亮氨酸和组氨酸通过mTOR信号通路调控奶牛腺上皮细胞中酪蛋白的合成

Leucine and histidine independently regulate milk protein synthesis in bovine mammary epithelial cells via mTOR signaling pathway 亮氨酸和组氨酸通过mTOR信号通路调控奶牛腺上皮细胞中酪蛋白的合成 1 2 3 4 first-author 1 3 4 1 3 4 corresp ‡Corresponding Author ‡Corresponding Author †E-mail:zhengnan_1980@126.com †E-mail:zhengnan_1980@126.com zhengnan_1980@126.com 1 3 4 Ministry of Agriculture-Milk Risk Assessment Laboratory, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China Ministry of Agriculture-Milk Risk Assessment Laboratory, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China Ministry of Agriculture-Milk and Dairy Product Inspection Center, Beijing 100193, China Ministry of Agriculture-Milk and Dairy Product Inspection Center, Beijing 100193, China State Key Laboratory of Animal Nutrition, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China State Key Laboratory of Animal Nutrition, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China The aim of this study is to investigate the effects of leucine (Leu) and histidine (His) on the expression of both the mammalian target of rapamycin (mTOR) signaling pathway-related proteins and caseins in immortalized bovine mammary epithelial cells (CMEC-H), using a single supplement through Western blotting. The Earle’s balanced salt solution (EBSS) was set as the control group and other treatment groups, based on the EBSS, were added with different concentrations of Leu or His, respectively. The results showed that, compared with the control group, the expression of caseins and the phosphorylation of mTOR (Ser 2481 ), Raptor (Ser 792 ), eIF4E (Ser 209 ), and eEF2 (Thr 56 ) increased with the Leu concentrations ranging from 0.45 to 10.80 mmol/L ( P < 0.01). The P-4EBP1 (Thr 37 ) at 10.80 mmol/L Leu, and P-RPS6 (Ser 235/236 ) at 5.40 to 10.80 mmol/L Leu all decreased. Similarly, the His supplementation from 0.15 to 9.60 mmol/L increased the expression of αs2-casein, β-casein, κ-casein, P-mTOR (Ser 2481 ), P-Raptor (Ser 792 ), P-S6K1 (Thr 389 ), P-4EBP1 (Thr 37 ), P-eIF4E (Ser 209 ), and P-eEF2 (Thr 56 ) ( P < 0.01) in CMEC-H, whereas the αs1-casein expression was only reduced at 9.60 mmol/L His, G protein β subunit-like protein (GβL) at 0.15 and 9.60 mmol/L His, and P-RPS6 at 4.80 to 9.60 mmol/L His. Our linear regression model assay suggested that the αs1-casein expression was positively correlated with P-mTOR ( P< 0.01), P-S6K1 ( P< 0.01), and P-eEF2 ( P< 0.01) for the addition of Leu, while the expressions of β-casein ( P< 0.01) and κ-casein ( P< 0.01) were positively correlated with P-eEF2 for the addition of His. In conclusion, the milk protein synthesis was up-regulated through activation of the mTOR pathway with the addition of Leu and His in CMEC-H. 目的 2 以体外培养的永生化奶牛乳腺上皮细胞（CMEC-H）为模型，利用蛋白免疫印迹法（Westernblotting）检测酪蛋白和哺乳动物雷帕霉素靶蛋白（mTOR）信号路径元件的蛋白磷酸化表达。进一步探索亮氨酸和组氨酸通过mTOR信号途径调控酪蛋白合成机制的重要意义。 创新点 2 首次在CMEC-H模型中研究不同浓度的亮氨酸和组氨酸通过mTOR复合物1（mTORC1）中mTOR（Ser 2481 ）、mTOR调控蛋白（Raptor，Ser 792 ）和G蛋白β亚基样蛋白（GβL）对酪蛋白表达调控的影响。研究证明mTOR（Ser 2448 ）并不是在乳腺上皮细胞中激活mTOR信号通路的唯一磷酸化位点，mTOR（Ser 2481 ）同样可作为激活mTOR信号通路的生物标记。 方法 2 以厄尔平衡溶液代替培养基，设为阴性对照，分别添加不同浓度的亮氨酸或组氨酸，利用Westernblotting检测酪蛋白和mTOR信号路径元件的蛋白表达。 结论 2 与阴性对照组相比，当在CMEC-H细胞中添加0.45~10.80mmol/L亮氨酸6h时，4种酪蛋白的表达和mTOR（Ser 2481 ）、Raptor（Ser 792 ）、真核翻译起始因子4E（eIF4E，Ser 209 ）和真核细胞翻译延伸因子（eEF2，Thr 56 ）的磷酸化表达均显著上调（ P < 0.01）。而当亮氨酸浓度在10.80mmol/L时，真核翻译起始因子4E结合蛋白1（4EBP1，Thr 37 ）的磷酸化表达被抑制；在5.40~10.80mmol/L时，核糖体蛋白S6（RPS6，Ser 235/236 ）的磷酸化被抑制。当添加0.15~9.60mmol/L组氨酸6h时，αs2-酪蛋白、β-酪蛋白、κ-酪蛋白的表达和mTOR（Ser 2481 ）、Raptor（Ser 792 ）、核糖体S6蛋白激酶（S6K1，Thr 389 ）、4EBP1（Thr 37 ）、eIF4E（Ser 209 ）和eEF2（Thr 56 ）的磷酸化表达均显著上调（ P < 0.01）。而当组氨酸浓度在9.60mmol/L时，αs1-酪蛋白的表达量降低；在0.15和9.60mmol/L时，GβL被抑制；在4.80~9.60mmol/L时，RPS6磷酸化被抑制。线性回归模型显示，当添加亮氨酸时，αs1-酪蛋白的表达与mTOR、S6K1和eEF2的磷酸化表达成显著的正相关（ P < 0.01；表4）；当添加组氨酸，β-酪蛋白和κ-酪蛋白均与eEF2磷酸化表达成显著的正相关（ P < 0.01；表5）。综上所述，在乳腺上皮细胞中，亮氨酸和组氨酸能通过mTOR信号通路促进酪蛋白基因的表达。 Bovine mammary epithelial cells Leucine Histidine Western blotting mTOR Casein 奶牛乳腺上皮细胞 亮氨酸 组氨酸 蛋白免疫印迹 mTOR 酪蛋白 Introduction 1 Dairy cow nutrient requirement systems regard essential amino acid (EAA) requirements in aggregate as metabolizable protein (MP), and presume a fixed efficiency of MP use for milk protein (Arriola Apelo et al., 2014b 2014b ). The composition of EAAs in MP vastly affects milk protein synthesis. Since the exact amount of limiting amino acids (LAAs) in dairy cow’s diets was unknown, cows were easily overfed to meet the balance of MP requirements, which leads to a waste of amino acids (AAs) and poor N efficiency (Bionaz et al., 2012 2012 ; Arriola Apelo et al., 2014a 2014a ). In current dairy production systems, an average of 25% of dietary N is captured in milk, which results in approximately 75% of the dietary N being excreted in urine and feces (Hristov et al., 2004 2004 ; Arriola Apelo et al., 2014b 2014b ). Feeding animals with low-protein diets (Kalscheur et al., 2006 2006 ) and supplementation of those deficient EAAs (lysine (Lys), methionine, leucine (Leu), isoleucine, valine, and histidine (His)) may maintain production, which can improve the total N efficiency (Kim et al., 2001 2001 ; Wang et al., 2010 2010 ; Appuhamy et al., 2011a 2011a ; 2012 2012 ), which is in accordance with Liebig’s hypothesis on developing the concept of the order of LAAs. This concept is commonly described by using the analogy of a water barrel with broken staves (Appuhamy et al., 2012 2012 ). The utilization of AAs is important for mammary protein synthesis in lactating cows (Appuhamy et al., 2012 2012 ; Arriola Apelo et al., 2014c 2014c ). Previous research on AA metabolism primarily focused on optimizing balanced diets, which is essential for maintaining and enhancing milk protein synthesis in dairy cattle (Hanigan et al., 2001 2001 ). AAs not only serve as a precursor for protein synthesis but also as signaling molecules that regulate the protein synthesis in mammalians (Kimball, 2002 2002 ; Arriola Apelo et al., 2014c 2014c ). A great number of reports have shown that AA-induced stimulation of milk protein synthesis is partially mediated by the mammalian target of rapamycin (mTOR), a protein kinase present in the rapamycin-sensitive mTOR complex 1 (mTORC1) (Yang et al., 2006 2006 ; Prizant and Barash, 2008 2008 ; Appuhamy et al., 2012 2012 ; Arriola Apelo et al., 2014c 2014c ). mTORC1 consists of mTOR, regulatory associated protein of TOR (Raptor), and a G protein β subunit-like protein (GβL) (Kim, 2009 2009 ). A great deal of evidence indicated that P-mTOR at Ser 2448 was an indicator of mTOR pathway activity in immortalized bovine mammary epithelial cells (MAC-T) (Appuhamy et al., 2011b 2011b ; 2012 2012 ). Prizant and Barash ( 2008 2008 ) showed that P-mTOR in Ser 2448 was completely inhibited by His supplementation, but phosphorylation of the ribosomal protein S6 kinase 1 (S6K1) and eukaryotic initiation factor 4E binding protein (4EBP1) could still be detected. AA supplementation may have contributed to other existent phosphorylation sites of mTOR that were not detected, resulting in phosphorylation of downstream effectors. Peterson et al. ( 2000 2000 ) and Gerasimovskaya et al. ( 2005 2005 ) demonstrated that the P-mTOR at Ser 2481 was also a good biomarker for mTOR pathway activation. Cheng et al. ( 2004 2004 ) demonstrated that the P-mTOR in Thr 2446 acted as a nutrient-regulated phosphorylation site located in the mTOR catalytic domain. We cannot exclude the possibility that phosphorylation of mTOR in Ser 2448 was important, yet it was not the only one regulating mTOR activity in bovine mammary epithelial cells (CMECs). Kim et al. ( 2002 2002 ) confirmed that P-Raptor is associated with mTOR and modulated by AAs, which regulate the mTOR kinase activity. When activated by AAs, mTORC1 in turn catalyzed S6K1 and 4EBP1 phosphorylation, followed by phosphorylating the ribosomal protein S6 (RPS6) (Wang and Proud, 2006 2006 ). S6K1 was a target of mTOR activated in Thr 389 whose phosphorylation status was a main indicator of the AA-induced mTORC1-activated signaling pathway (Moshel et al., 2006 2006 ; Prizant and Barash, 2008 2008 ; Appuhamy et al., 2012 2012 ; Arriola Apelo et al., 2014c 2014c ). In addition, phosphorylation of 4EBP1 by mTOR increased the initial reaction rates (Beugnet et al., 2003 2003 ). When 4EBP1 was activated, the expression of a regulatory protein binding into the mRNA cap-binding protein eukaryotic initiation factor 4E (eIF4E) was also promoted. When 4EBP1 was unphosphorylated, cap-dependent translation was inhibited by competitively blocking the binding of eukaryotic translation initiation factor 4G (eIF4G) to eIF4E (Gingras et al., 1999 1999 ; Harris and Lawrence, 2003 2003 ). The elongation step of mRNA translation was enhanced by eukaryotic elongation factor 2 (eEF2) (Wang and Proud, 2006 2006 ) and was inhibited by its phosphorylation on Thr 56 , which suggested that eEF2 may be a limiting factor in milk protein synthesis (Christophersen et al., 2002 2002 ; Appuhamy et al., 2011b 2011b ). These studies have shown that Leu and His in addition to Lys and Met are main LAAs in forage diets (Kim et al., 2001 2001 ; Korhonen et al., 2002 2002 ). Leu, a branched chain amino acid (BCAA), is currently the most prevalent EAA in the diet (Korhonen et al., 2002 2002 ; Appuhamy et al., 2012 2012 ). According to previous reports, Leu was involved in cell growth and differentiation through the mTOR pathway (Proud, 2007 2007 ; Stipanuk, 2007 2007 ). Moreover, Leu produced a dose-dependent regulation of mTOR and served as a key intracellular regulatory factor of the mTORC1 pathway in CMECs (Moshel et al., 2006 2006 ; Prizant and Barash, 2008 2008 ; Appuhamy et al., 2012 2012 ; Durán and Hall, 2012 2012 ). Kim et al. ( 2001 2001 ) found that His was the first limiting factor for milk protein secretion. Some traditional experiments indicated that the perfusion of His promoted milk protein synthesis (Bequette et al., 2000 2000 ). Likewise, some cell experiments demonstrated that the addition of His activated the mTOR pathway, which up-regulated phosphorylation of the downstream protein and ultimately promoted milk protein synthesis (Appuhamy et al., 2012 2012 ). Prizant and Barash ( 2008 2008 ) also reported that His was a key intracellular regulatory factor of the mTORC1 pathway in L-1 cells, a cloned cell line derived from lactating bovine mammary gland, however, negatively regulated P-S6K1, and decreased the β-casein synthesis rate. So, it is meaningful to explore the mechanism of how His influenced the mTOR pathway. We hypothesize that AAs affect milk protein synthesis in CMEC-H through phosphorylation of translation factors of the mTOR signaling pathway. Although the effects of EAAs on mTOR cell signaling and milk protein synthesis have been extensively explored (Moshel et al., 2006 2006 ; Burgos and Cant, 2010 2010 ; Toerien et al., 2010 2010 ), effects of different levels of Leu or His on phosphorylation of Raptor on Ser 792 , mTOR on Ser 2481 , and GβL expression involved in casein protein synthesis were not clear in bovine mammary cells. Our study investigated the regulatory effects of different concentrations of Leu and His on the mTOR signaling pathway and the relationships between these signaling protein activities with milk protein synthesis. Materials and methods 1 In the present study, all animal care and experimental procedures were approved and conducted under the established standards of the Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China. Unless otherwise stated, all components were purchased from the Sigma-Aldrich Shanghai Trading Co. Ltd. (Shanghai, China). The Dulbecco’s modified Eagle’s medium (DMEM)/Ham’s F12 (diluted 1:1 (v/v), 1439945/1491066, Invitrogen Trading Co. Ltd., China) was used as the basal growth medium, supplemented with 10% fetal bovine serum (FBS) (Invitrogen Trading Co. Ltd., China) and 100 μg/ml penicillin-streptomycin solution (C0222, Beyotime Institute of Biotechnology, China). The differentiation medium contained bovine insulin, progesterone, bovine holo-transferrin, hydrocortisone, bovine epithelial growth factor, and bovine estradiol (Sigma-Aldrich, Cat. Nos. I4434, T1283, P8783, H0888, E4127, and E2758, respectively). Individual AAs (L-Leu and L-His, Cat. Nos. L8912 and H5659, respectively) were purchased from the Sigma-Aldrich Shanghai Trading Co. Ltd., China. The non-and site-specific phosphorylated antibodies against mTOR (Ser 2481 , YT2913/YP1134), 4EBP1 (Thr 37 , YT0018/YP0001), RPS6 (Ser 235/236 , YT4139/YP0832), and eIF4E (Ser 209 , YT1516/YP0094) were purchased from Immuno Way. The total and site-specific phosphorylated antibodies against Raptor (Ser 792 , No. 2280/2083), S6K1 (Thr 389 , No. 9202/9205), eEF2 (Thr 56 , No. 2332/2331), and GβL (No. 3274) were purchased from Cell Signaling Technology (Danvers, MA, USA). The αs1-casein antibody (SAB1401093) and κ-casein antibody (SAB1401094) were purchased from Sigma-Aldrich Shanghai Trading Co., Ltd. China, the αs2-casein antibody (bs-10034R) was purchased from Bioss (Beijing Biosynthesis Biotechnology Co., Ltd., China) and the β-casein antibody (orb18512) was purchased from Biorbyt (Cambridge, UK). β-Actin (ab8226), used as a loading control, was purchased from Abcam Trading (Shanghai) Company Ltd. (China). Cell culture and experimental design 2 The immortalized bovine mammary epithelial cell line (CMEC-H) was established in our previous work (Hu et al., 2014 2014 ). The cells were cultured at 37 °C with 5% CO 2 and digested with 0.25% (2.5 g/L) trypsin-0.02% etilendiaminetetraacetic acid (EDTA) (C0203, Beyotime Institute of Biotechnology, China). The Earle’s balanced salt solution (EBSS, CC0043, Leagene Biotechnology, China) was used as a substitute of medium without AAs (Table 1 1 ), and was set as a negative control in the experimental design. The EBSS was supplemented with 10% FBS and was used as a positive control. The concentrations of Leu and His in the DMEM/F12 medium were 0.45 and 0.15 mmol/L, respectively. EAAs were added according to the concentrations described in Tables 2 2 and 3 3 . The CMEC-H cells were cultured in 9-cm plates (172958, Thermo Scientific, China) to 80% confluence and induced to be differentiated by the differentiation medium for 24 h. The differentiated CMEC-H cells were incubated in serum-free, complete DMEM/F12 media overnight. Leu or His was supplemented individually for 6 h at the indicated concentrations. Each experiment was triplicated and each of the whole experiments was repeated three times on three different days. Modified from Gao et al. ( 2015 2015 ) Component Concentration (mmol/L)  Anhydrous CaCl 2 1.050  CuSO 4 ∙5H 2 O 5.2×10 −6  Fe(NO 3 ) 3 ∙9H 2 O 1.238×10 −4  FeSO 4 ∙7H 2 O 0.002  Anhydrous MgCl 2 0.301  Anhydrous MgSO 4 0.407  KCl 4.157  NaHCO 3 14.286  NaCl 120.612  Anhydrous Na 2 HPO 4 0.500  NaH 2 PO 4 ∙H 2 O 0.453  ZnSO 4 ∙7H 2 O 0.002  D-Glucose (dextrose) 17.506  Phenol red 0.022 DMEM/F12 base media contained leucine (0.45 mmol/L) at a level sufficient for normal cellular processes. +: add Group EBSS Leu (mmol/L) 10% FBS Negative control + Positive control + + 4 Treatment + 0.45 + 1.35 + 5.40 + 10.80 DMEM/F12 base media contained histidine (0.14999 mmol/L) at a level sufficient for normal cellular processes. +: add Group EBSS His (mmol/L) 10% FBS Negative control + Positive control + + 4 Treatment + 0.15 + 1.20 + 4.80 + 9.60 Protein immunoblot analysis 2 The cell samples were homogenized in an ice-cold radio immunoprecipitation assay (RIPA) buffer (P0013, Beyotime Institute of Biotechnology, China) containing 1 mmol/L phenylmethylsulfonyl fluoride (PMSF), 1% (v/v) protease, and a phosphatase inhibitor cocktail (78430, Thermo Scientific). Cell lysates were centrifuged at 2000× g for 3 min and the supernatants were transferred to new tubes. The protein concentrations of the samples were determined by bicinchoninic acid (BCA) assay kits (P0010S, Beyotime Institute of Biotechnology, China). The lysates (30 μg of protein) were loaded onto gels, separated by 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and blotted onto polyvinylidene fluoride (PVDF) transfer membranes (0.45 and 0.2 μmol/L immobilon-P, IPVH00010 and ISEQ00010, Millipore). The membranes were blocked for 1 h (blot-PO buffer, WBAVDP001, Millipore) and incubated overnight at 4 °C in primary antibodies (appropriately diluted 1:1000 in phosphate-buffered saline (PBS)) against total and site-specific phosphorylated mTOR (Ser 2481 ), 4EBP1 (Thr 37 ), RPS6 (Ser 235/236 ), eIF4E (Ser 209 ), Raptor (Ser 792 ), S6K1 (Thr 389 ), eEF2 (Thr 56 ), and GβL. The amounts of synthesized milk proteins were determined by antibodies against αs1-casein (1:1000), αs2-casein (1:400), β-casein (1:500), and κ-casein (1:1000). The blots were washed three times with Tris-buffered saline containing 0.02% (v/v) Tween-20 (TBST), and then incubated with a second antibody (anti-rabbit IgG, A9169, Sigma; anti-goat IgG, AP106P, Millipore; anti-Mouse IgG, A9044, Sigma) and diluted at 1:5000 in PBS. Immunoreactive bands were visualized by Pierce ECL Western Blotting Substrate kits (32106, Thermo Scientific) according to the manufacturer’s instructions and were then exposed to X-ray film. The protein band densities were determined by the Image J2x 2.1.4.7 Analyzer (Rawak Software, Inc., Germany). The relative values from the AA-supplemented cells were related to their AA-deprived controls. Statistical analysis 2 At least three independent experiments were done with identical results and all data were tested using the Duncan’s test for post-hoc multiple comparisons of treatment means by SAS software (SAS 9.2 Inst., Cary, NC, USA). Differences between experimental groups were considered significant at a P -value of < 0.05. The random effect in the one-way analysis of variance (ANOVA) model was replicated and the fixed effect was the levels of Leu and His. Meaningful relationships among the phosphorylation state of the signaling proteins and casein protein expression in CMEC-H were quantified with simple linear regression models using the REG procedure of SAS. Results 1 Effects of Leu or His supplementation on the expression of caseins 2 Compared with the negative control group, our data demonstrated that the addition of Leu to EBSS generated dose-responsive effects on the casein expression. Figs. 1a and 1b 1a and 1b show that Leu had stimulatory effects on the casein expression in the range of 0.45 to 10.80 mmol/L. Specific to each casein, αs1-casein, αs2-casein, β-casein, and κ-casein reached their highest expression at 0.45, 1.35, 5.40, and 10.80 mmol/L Leu with an increase of 260%, 66%, 150%, and 270%, respectively. Figs. 1c and 1d 1c and 1d show the effects of His supplementation on the casein expression. Compared with the negative control, the expression of casein was all promoted by His in the range of 0.15 to 9.60 mmol/L, except that αs1-casein expression was decreased at 9.6 mmol/L His. In addition, each casein, αs1-casein, αs2-casein, β-casein, and κ-casein reached their highest expression at 4.80, 1.20, 0.15, and 0.15 mmol/L His with 1.6-, 1.8-, 1.8-, and 1.8-fold changes, respectively. (a) Leu was supplemented for 6 h at the indicated concentrations. Casein levels were determined by immunoblot analysis. Numbers above the lanes refer to the levels (mmol/L) of the supplemented Leu relative to that in the Earle’s balanced salt solution. (b) Densitometric analysis of signals obtained from the casein immunoblot (a). (c) His was supplemented for 6 h at the indicated concentrations. Casein levels were determined by immunoblot analysis. Numbers above the lanes refer to the levels (mmol/L) of the supplemented His relative to that in the Earle’s balanced salt solution. (d) Densitometric analysis of signals obtained from the casein immunoblot (c). β-Actin was assessed as a loading control. A representative blot and quantitation of three independent experiments were shown. In all panels, data represent the mean±SD. E: Earle’s balanced salt solution; E+10% FBS: Earle’s balanced salt solution supplemented with 10% fetal bovine serum. Data in the same concentration marked with different letters represent a significant difference ( P < 0.05) Effects of Leu or His supplementation on the expression of mTORC1 2 Our results indicated that the Leu supplementation affected the phosphorylation of mTORC1 in a dose-dependent manner. Figs. 2a and 2b 2a and 2b show that, compared with the negative control group, only the P-Raptor was markedly increased with the addition of Leu from 0.45 to 10.80 mmol/L. The GβL expression at 10.80 mmol/L Leu and mTOR phosphorylation at 0.45 and 10.80 mmol/L Leu were not significantly changed, and they were significantly enhanced at other concentrations. The changes of mTORC1 all reached their summit at 5.40 mmol/L Leu. Figs. 2c and 2d 2c and 2d show the influence of His supplementation on mTORC1. P-Raptor was dramatically increased from 0.15 to 9.60 mmol/L His. The P-mTOR and GβL expression were slightly enhanced in the full concentration range, except that the GβL expression was subtly reduced at 0.15 and 9.60 mmol/L His. (a) Leu was supplemented for 6 h at the indicated concentrations. mTORC1 levels were determined by immunoblot analysis. Numbers above the lanes refer to the levels (mmol/L) of the supplemented Leu relative to that in the Earle’s balanced salt solution. (b) Densitometric analysis of signals obtained from the mTORC1 immunoblot (a). (c) His was supplemented for 6 h at the indicated concentrations. mTORC1 levels were determined by immunoblot analysis. Numbers above the lanes refer to the levels (mmol/L) of the supplemented His relative to that in the Earle’s balanced salt solution. (d) Densitometric analysis of signals obtained from the mTORC1 immunoblot (c). β-Actin was assessed as a loading control. A representative blot and quantitation of three independent experiments were shown. In all panels, data represent the mean±SD. E: Earle’s balanced salt solution; E+10% FBS: Earle’s balanced salt solution supplemented with 10% fetal bovine serum. Data in the same concentration marked with different letters represent a significant difference ( P < 0.05) Effects of Leu or His level on the expression of mTOR downstream signaling proteins 2 Figs. 3a and 3b 3a and 3b show that Leu had obvious stimulatory effects on phosphorylation of eEF2 and eIF4E compared to the negative control group, while S6K1 phosphorylation with the addition of Leu was not significantly changed except at 0.45 mmol/L Leu with 2.2-fold changes. For 4EBP1 phosphorylation, its enhancement was observed from 0.45 to 5.40 mmol/L Leu, while 10.80 mmol/L Leu impaired its phosphorylation. Leu supplementation had a minor enhancing effect on the RPS6 phosphorylation level between 0.45 and 1.35 mmol/L, while the phosphorylation level was inhibited over 1.35 mmol/L Leu. Figs. 3c and 3d 3c and 3d suggest that His supplementation up-regulated all of the studied mTOR downstream proteins in the full concentration range except P-RPS6 at 9.60 mmol/L His and S6K1 phosphorylation which increased in a dose-dependent manner. In addition, at 9.60 mmol/L His, P-S6K1 was nearly 7 times greater than that of the control group. The phosphorylation of 4EBP1 reached its peak ( P < 0.01) at 1.20 mmol/L His. It was noteworthy that P-RPS6 at 0.15 mmol/L His was 20 times greater than that of the control group. (a) Leu was supplemented for 6 h at the indicated concentrations. mTOR downstream signaling protein levels were determined by immunoblot analysis. Numbers above the lanes refer to the levels (mmol/L) of the supplemented Leu relative to that in the Earle’s balanced salt solution. (b) Densitometric analysis of signals obtained from the mTOR downstream signaling protein immunoblot (a). (c) His was supplemented for 6 h at the indicated concentrations. mTOR downstream signaling protein levels were determined by immunoblot analysis. Numbers above the lanes refer to the levels (mmol/L) of the supplemented His relative to that in the Earle’s balanced salt solution. (d) Densitometric analysis of signals obtained from the mTOR downstream signaling protein immunoblot (c). β-Actin was assessed as a loading control. A representative blot and quantitation of three independent experiments were shown. In all panels, data represent the mean±SD. E: Earle’s balanced salt solution; E+10% FBS: Earle’s balanced salt solution supplemented with 10% fetal bovine serum. Data in the same concentration marked with different letters represent a significant difference ( P < 0.05) Relationships between casein expression and mTOR pathway-related protein changes with Leu supplementation 2 A simple linear regression model assay demonstrated that αs1-casein expression was positively associated with phosphorylation of mTOR, GβL, Raptor, S6K1, 4EBP1, eEF2, RPS6, and eIF4E ( P < 0.01), respectively (Table 4 4 ). With the addition of Leu, a 1-fold increase in αs1-casein expression was related to 4.85-, 2.04-, 1.15-, 2.48-, 2.44-, 8.14-, 1.41-, and 2.12-fold changes in mTOR, GβL, Raptor, S6K1, 4EBP1, eEF2, RPS6, and eIF4E phosphorylation, respectively. A notably positive relationship ( R 2 =0.7820, 0.5815, 0.7881, 0.7835, and 0.6164; P < 0.01) was found between αs1-casein expression and mTOR, GβL, S6K1, eEF2 and eIF4E phosphorylation, respectively. No phosphorylation of other mTOR signaling proteins explained the further variation in αs1-casein protein expression in CMEC-H (Table 4 4 ). Dependent variable Independent variable P -value Regression coefficient R 2 αs1-casein mTOR 0.0001 4.84738 0.7820 GβL 0.0001 2.03558 0.5815 Raptor 0.0052 1.15177 0.3572 S6K1 0.0001 2.48016 0.7881 4EBP1 0.0010 2.44002 0.4710 eEF2 0.0001 8.14314 0.7835 RPS6 0.0087 1.40988 0.3179 eIF4E 0.0001 2.11775 0.6164 αs2-casein mTOR 0.0285 0.41805 0.2200 GβL 0.0046 0.24768 0.3663 Raptor 0.0001 0.21865 0.6179 S6K1 0.0008 0.29594 0.4823 4EBP1 0.0172 0.28417 0.2630 eEF2 0.0341 0.68184 0.2043 RPS6 0.3133 0.08850 0.0049 eIF4E 0.0021 0.26688 0.4225 β-casein mTOR 0.0170 1.20726 0.2638 GβL 0.0013 0.73002 0.4534 Raptor 0.0001 0.60842 0.6670 S6K1 0.0068 0.68103 0.3370 4EBP1 0.4660 0.25321 −0.0267 eEF2 0.0188 2.00066 0.2556 RPS6 0.4630 −0.17444 −0.0262 eIF4E 0.0013 0.73944 0.4531 κ-casein mTOR 0.2831 0.82785 0.0136 GβL 0.6733 0.15885 −0.0504 Raptor 0.0018 0.71268 0.4338 S6K1 0.0475 0.74591 0.1751 4EBP1 0.2856 −0.52169 0.0128 eEF2 0.2485 1.48963 0.0249 RPS6 0.0626 −0.60010 0.1503 eIF4E 0.0017 1.03420 0.4375 The αs2-casein expression was positively correlated with phosphorylation of mTOR, GβL, Raptor, S6K1, 4EBP1, eEF2, and eIF4E ( P < 0.05), respectively (Table 4 4 ). A 1-fold increase in αs2-casein protein expression was related to 0.42-, 0.25-, 0.22-, 0.30-, 0.28-, 0.68-, and 0.27-fold changes in mTOR, GβL, Raptor, S6K1, 4EBP1, eEF2, and eIF4E phosphorylation, respectively. However, Raptor phosphorylation appeared to be the primary driver when computed in a multivariate model, which explained 61.79% of the observed variation (Table 4 4 ). The β-casein expression was positively associated with phosphorylation of mTOR, GβL, Raptor, S6K1, eEF2, and eIF4E ( P < 0.05), respectively (Table 4 4 ). A 1-fold increase in the β-casein protein expression was related to 1.21-, 0.73-, 0.61-, 0.68-, 2.00-, and 0.74-fold changes in mTOR, GβL, Raptor, S6K1, eEF2, and eIF4E phosphorylation, respectively. A notably positive relationship ( R 2 =0.6670, P < 0.01) was found between the β-casein expression and P-Raptor, while no correlations were found between the expression of β-casein and phosphorylation of 4EBP1 ( P =0.4660) or RPS6 ( P =0.4630) in CMEC-H (Table 4 4 ). The κ-casein expression was positively associated with phosphorylation of Raptor, S6K1, and eIF4E ( P < 0.05), respectively (Table 4 4 ). No correlations were found between the κ-casein expression and phosphorylation of mTOR ( P =0.2831), GβL ( P =0.6733), 4EBP1 ( P =0.2856), eEF2 ( P =0.2485), or RPS6 ( P =0.0626) in CMEC-H (Table 4 4 ). Relationships between casein expression and mTOR pathway-related protein changes with His supplementation 2 The expression of αs1-casein was positively correlated with phosphorylation of mTOR, GβL, and eEF2 ( P < 0.05), respectively (Table 5 5 ). A 1-fold increase in the αs1-casein expression was related to 0.59-, 0.60-, and 0.14-fold changes in mTOR, GβL, and eEF2 phosphorylation, respectively. A notable positive relationship ( R 2 =0.5133, P < 0.01) was found between the αs1-casein expression and eEF2 phosphorylation. Dependent variable Independent variable P -value Regression coefficient R 2 αs1-casein mTOR 0.0023 0.58689 0.4149 GβL 0.0234 0.60173 0.2370 Raptor 0.5879 0.02210 −0.0424 S6K1 0.1926 0.10670 0.0476 4EBP1 0.3503 0.05559 −0.0044 eEF2 0.0005 0.13542 0.5133 RPS6 0.3110 0.01383 0.0055 eIF4E 0.1374 0.08256 0.0784 αs2-casein mTOR 0.0007 0.60885 0.4954 GβL 0.0018 0.74109 0.4307 Raptor 0.0598 0.07033 0.1544 S6K1 0.0020 0.21580 0.4267 4EBP1 0.0001 0.17724 0.5790 eEF2 0.1536 0.06191 0.0682 RPS6 0.9829 0.00029 −0.0625 eIF4E 0.0029 0.14346 0.3995 β-casein mTOR 0.0003 1.22687 0.5341 GβL 0.0263 1.10642 0.2271 Raptor 0.3081 0.07720 0.0063 S6K1 0.0628 0.27713 0.1500 4EBP1 0.2005 0.14074 0.0440 eEF2 0.0001 0.33806 0.9638 RPS6 0.0003 0.07675 0.5368 eIF4E 0.0049 0.26810 0.3624 κ-casein mTOR 0.0006 0.85113 0.5050 GβL 0.0544 0.69444 0.1629 raptor 0.1936 0.06931 0.0472 S6K1 0.0501 0.20637 0.1704 4EBP1 0.2484 0.09071 0.0250 eEF2 0.0001 0.23346 0.9048 RPS6 0.0001 0.05838 0.6228 eIF4E 0.0015 0.20877 0.4464 The αs2-casein expression was positively associated with phosphorylation of mTOR, GβL, S6K1, 4EBP1, and eIF4E ( P < 0.01), respectively (Table 5 5 ). A 1-fold increase in the αs2-casein expression was related to 0.61-, 0.74-, 0.22-, 0.18-, and 0.14-fold changes in mTOR, GβL, S6K1, 4EBP1, and eIF4E phosphorylation, respectively. A positive relationship ( R 2 =0.5790, P < 0.01) was found between the αs2-casein expression and P-4EBP1. The β-casein expression was positively associated with phosphorylation of mTOR, GβL, eEF2, RPS6, and eIF4E ( P < 0.05), respectively (Table 5 5 ). A 1-fold increase in the β-casein expression was related to 1.23-, 1.11-, 0.34-, and 0.27-fold changes in mTOR, GβL, eEF2, and eIF4E phosphorylation, respectively. A notable positive relationship ( R 2 =0.5341, 0.9638, and 0.5368, P < 0.01) was found between the β-casein expression and mTOR, eEF2 and RPS6 phosphorylation, respectively. The κ-casein expression was positively associated with phosphorylation of mTOR, eEF2, RPS6, and eIF4E ( P < 0.01), respectively (Table 5 5 ). A 1-fold increase in the κ-casein expression was related to 0.85-, 0.23-, and 0.21-fold changes in mTOR, eEF2, and eIF4E phosphorylation, respectively. A notable positive relationship ( R 2 =0.5050, 0.9048, and 0.6228, P < 0.01) was found between the κ-casein expression and mTOR, eEF2 and RPS6 phosphorylation, respectively. Discussion 1 In this paper, the functions and potential molecular mechanisms of Leu and His effects on the mTOR signaling pathway in the regulation of milk protein synthesis were studied. In order to eliminate the impact of the other AAs on CMEC-H, all AAs were removed from EBSS and Leu or His was then individually added to it. In our study, all four forms of caseins were up-regulated by Leu or His supplementation with the exception of 9.60 mmol/L His on αs1-casein, which supported the notion that both Leu and His are key limiting factors for milk protein synthesis. It is widely accepted that mTOR is a key regulator of milk protein synthesis and most reports were concerned with the role of AAs in the regulation of P-mTOR on Ser 2448 in milk protein synthesis (Prizant and Barash, 2008 2008 ; Appuhamy et al., 2012 2012 ; Arriola Apelo et al., 2014c 2014c ). Here we identify another mTOR phosphorylation site on Ser 2481 as an indicator of activated mTOR pathway in CMEC-H, which was increased by the addition of Leu or His in the full concentration range. An exception to this was the supplementation of Leu at 0.45 mmol/L with no obvious change. This data indicated that P-mTOR on Ser 2481 could act as an alternative switch to integrate signals from Leu and His to regulate protein translation. The effects of Leu and His supplementation on two other mTORC1 components, Raptor and GβL, were also studied. The association between Raptor and mTOR was manipulated by AAs. Raptor acts as a scaffold protein regulating the assembly, localization, and substrate binding of mTORC1 (Laplante and Sabatini, 2012 2012 ), and it is also used for the mTOR-catalyzed phosphorylation of 4EBP1 and mediates TOR action in vivo (Hara et al., 2002 2002 ). With AA deprivation, the mTOR kinase activity is inactive (Kim et al., 2013 2013 ). The addition of Leu and His activates mTOR kinase to increase the Raptor expression (Kim et al., 2002 2002 ). GβL also plays a positive role in mTOR activation by AA supplementation. The binding of GβL to the mTOR kinase domain stabilized the interaction between the Raptor and mTOR (Kim et al., 2003 2003 ). Our results indicated that Raptor notably increased (1.8 and 4.7 times) in comparison with the control group, when added Leu and His, respectively. GβL expression increased in the range of 0.45 and 5.40 mmol/L of Leu with a 2.5-fold change in comparison with the control, whereas His supplementation slightly enhanced GβL expression in the same range. Both GβL and P-mTOR demonstrated the highest changes at 5.40 mmol/L Leu or 4.80 mmol/L His. Previous studies indicated that GβL positively correlated with P-mTOR on Ser 2448 (Kim et al., 2003 2003 ), and that there was a strong relationship between GβL and P-mTOR on Ser 2481 . S6K1, a major downstream target of mTOR, serves as an indicator of activation of the mTORC1 pathway (Yang et al., 2006 2006 ; Prizant and Barash, 2008 2008 ; Appuhamy et al., 2012 2012 ; Arriola Apelo et al., 2014c 2014c ). As most reports showed, 0.45 mmol/L Leu dramatically increased S6K1 phosphorylation. The effect of Leu concentrations greater than 0.45 mmol/L on S6K1 phosphorylation was monitored, and there was no obvious change in comparison with the control group. P-S6K1 increased along with His supplementation in the full concentration range. This was in contrast to the negative effects of His on P-S6K1 in CMECs reported by Prizant and Barash ( 2008 2008 ). However, as a whole, P-S6K1 has a dose-dependent effect from His concentration. However, our results support the traditional perfused experiment in which His was positively associated with P-S6K1 in dairy cows (Toerien et al., 2010 2010 ). The difference between those two studies was potentially due to the different time response of the His addition. In the study of Prizant and Barash ( 2008 2008 ), CMECs were incubated in His for 10 min; however, in our study 6 h was used for incubation. We thought after starvation, the CMECs were in a stress period responding to the His addition in a short time, because they needed a period to repair the damages resulting from the devoid of AAs. So the addition of His may first maintain the cell survival instead of proving the milk synthesis. 4EBP1 is another major downstream target of mTOR (Li et al., 2005 2005 ). Activated mTOR regulates protein translation by directly inducing P-4EBP1. Our results indicated that the addition of Leu and His to the EBSS increased P-4EBP1 in CMEC-H. Furthermore, only the highest concentrations of Leu inhibited its phosphorylation, which further validated the notion that 4EBP1 was up-regulated by mTOR. RPS6 is phosphorylated by S6K1. In our study, Leu supplementation slightly improved RPS6 phosphorylation levels between 0.45 and 1.35 mmol/L, while the phosphorylation level was inhibited over 1.35 mmol/L. As a substrate of S6K1, RPS6 was positively correlated with S6K1 phosphorylation between 0.45 and 1.35 mmol/L Leu, which was consistent with the results of Appuhamy et al. ( 2012 2012 ) that focused on 0.45 mmol/L Leu. On the other hand, His supplementation vastly enhanced the RPS6 phosphorylation level at 0.15 mmol/L, followed by a sharply decreased phosphorylation level between 1.20 and 9.60 mmol/L. Our study revealed that there may have been a negative feedback between RPS6 and S6K1 beyond 1.35 mmol/L Leu or 0.15 mmol/L His supplementation. The eIF4E is involved in directing ribosomes to the cap structure of mRNAs (Stipanuk, 2007 2007 ). The mTORC1 phosphorylates 4EBP1 to release eIF4E from the 4EBP1-eIF4E complex, thus promoting eIF4E-dependent translation initiation. The stimulatory effects of His and Leu supplementation on the phosphorylation of eIF4E in CMECs were notably enhanced, which was in accordance with P-4EBP1 changes. The eEF2 was known to catalyze the mRNA translocation step in the elongation process during protein synthesis (Kaul et al., 2011 2011 ). Compared with initiation, eEF2 may be an important factor and is likely to be a rate-limiting enzyme for milk protein synthesis under AA-deprived conditions in the mammary gland of cows only in late-lactation because it consumes more energy in elongation (Merrick, 1992 1992 ; Wilde et al., 1997 1997 ; Christophersen et al., 2002 2002 ). Direct spatially-controlled inhibition of eEF2 phosphorylation induces local translational activation (Li et al., 2005 2005 ; Kaul et al., 2011 2011 ). Our study demonstrated that both Leu and His ( P < 0.01) enhanced eEF2 phosphorylation levels in comparison with a negative control. However, Leu supplementation had enhanced eEF2 phosphorylation by no more than a 20% increase. A linear regression model was employed to analyze the relationships among EAA, milk protein and mTOR pathway-related proteins. Appuhamy et al. ( 2014 2014 ) reported that intracellular EAA tended ( P =0.09) to positively affect mTOR phosphorylation, and the phosphorylation of mTOR ( P < 0.01) was positively associated with fractional rates of mammary protein synthesis (FSR) in bovine mammary tissue slices. Consistently, in the current work, a 1-fold increase in mTOR phosphorylation and GβL expression was associated with a remarkable increase in αs1-casein, αs2-casein, and β-casein expression ( P < 0.05), provision of extracellular Leu and His in CMEC-H. However, Leu supplementation on four casein expressions explained 115%, 22%, 60%, and 71% ( P < 0.01), respectively, of the variability in Raptor phosphorylation. Alternatively, the addition of His to casein protein expression was insignificantly associated with Raptor phosphorylation ( P =0.59, 0.06, 0.31, and 0.19, respectively). Both Leu and His significantly increased mTOR phosphorylation. Leu significantly activated phosphorylation of S6K1, which enhanced four casein expressions in CMEC-H ( P < 0.05). However, when the addition of His was analyzed with the same regression model, the S6K1 phosphorylation had a notable association with αs2-casein and κ-casein ( P < 0.05). With the addition of Leu or His, αs1-casein was positively related to eEF2 phosphorylation ( P < 0.01) in CMEC-H. In previous experiments, P-eEF2 was associated with P-mTOR, which tended ( P =0.10) to impose a negative effect on casein synthesis rates, independent of mTOR phosphorylation (Appuhamy et al., 2014 2014 ). Therefore, the inconsistent results of the effects of Leu and His on eEF2 phosphorylation could be due to different substitutes of the medium. In our study, we did not contain AAs and insulin, while insulin and nonessential amino acids (NEAAs) were present in the medium of the study of Appuhamy et al. ( 2012 2012 ). It is possible that the potential presence of greater nutrients in substituting in the medium may have partly masked the single AA effects on the cellular status in CMECs. We believe that the interaction of AAs and insulin is more significant than the influence of adding a single AA on mTOR pathways. Conclusions 1 In summary, the results of this study demonstrated that Leu or His supplementation stimulated αs-casein, β-casein, and κ-casein expression. Casein expression, P-mTOR (Ser 2481 ), P-Raptor (Ser 792 ), P-eIF4E (Ser 209 ), and P-eEF2 (Thr 56 ) increased with Leu concentration in the range of 0.45 to 10.80 mmol/L. Leu supplementation suppressed P-4EBP1 (Thr 37 ) at 10.80 mmol/L, and inhibited P-RPS6 (Ser 235/236 ) over 5.40 mmol/L. Supplementing His from 0.15 to 9.60 mmol/L increased the αs2-casein, β-casein, and κ-casein expression and phosphorylation of S6K1 (Thr 389 ), 4EBP1 (Thr 37 ), eIF4E (Ser 209 ), and eEF2 (Thr 56 ) in CMEC-H cells, at 0.15 and 9.60 mmol/L reduced the GβL expression, and over 4.80 mmol/L inhibited RPS6 (Ser 235/236 ). When adding Leu, the αs1-casein was positively correlated with P-mTOR (Ser 2481 ) ( R 2 =0.7820, P < 0.01) and P-S6K1 (Thr 389 ) ( R 2 =0.7881, P < 0.01), respectively. With the addition of His, eEF2 was positively correlated with β-casein ( R 2 =0.9638, P < 0.01) and κ-casein ( R 2 =0.9048, P < 0.01), respectively. Our results provide basic information for further study to clarify the regulation mechanism of Leu and His on casein expression through the mTOR pathway in the dairy cattle mammary gland. References JA Appuhamy , JR Knapp , O Becvar , 等 . 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All institutional and national guidelines for the care and use of laboratory animals were followed. 10.1631/jzus.B1400337 Project supported by the National Basic Research Program (973) of China (No. 2011CB100805), the Modern Agro-Industry Technology Research System of China (No. nycytx-04-01), and the Agricultural Science and Technology Innovation Program (No. ASTIP-IAS12), China 2014-11-30 2015-05-25 2015-05-23 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2015 2015 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 06 16