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SESN2 negatively regulates cell proliferation and casein synthesis by inhibition the amino acid-mediated mTORC1 pathway in cow mammary epithelial cells

机译:SESN2通过抑制牛乳腺上皮细胞中氨基酸介导的mTORC1途径来负调节细胞增殖和酪蛋白合成

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摘要

Amino acids (AA) are one of the key nutrients that regulate cell proliferation and casein synthesis in cow mammary epithelial cells (CMEC), but the mechanism of this regulation is not yet clear. In this study, the effect of SESN2 on AA-mediated cell proliferation and casein synthesis in CMEC was assessed. After 12 h of AA starvation, CMECs were cultured in the absence of all AA (AA−), in the presences of only essential AA (EAA+), or of all AA (AA+). Cell proliferation, casein expression, and activation of the mammalian target of rapamycin complex 1 (mTORC1) pathway were increased; but SESN2 expression was decreased in response to increased EAA or AA supply. Overexpressing or inhibiting SESN2 demonstrated that cell proliferation, casein expression, and activation of the mTORC1 pathway were all controlled by SESN2 expression. Furthermore, the increase in cell proliferation, casein expression, and activation of the mTORC1 pathway in response to AA supply was inhibited by overexpressing SESN2, and those effects were reversed by inhibiting SESN2. These results indicate that SESN2 is an important inhibitor of mTORC1 in CMEC blocking AA-mediated cell proliferation and casein synthesis.
机译:氨基酸(AA)是调节牛乳腺上皮细胞(CMEC)中细胞增殖和酪蛋白合成的关键营养素之一,但这种调节的机制尚不清楚。在这项研究中,评估了SESN2对CMEC中AA介导的细胞增殖和酪蛋白合成的影响。饥饿12小时后,在不存在所有AA(AA-),仅存在必需AA(EAA +)或所有AA(AA +)的情况下培养CMEC。细胞增殖,酪蛋白表达和雷帕霉素复合物1(mTORC1)途径的哺乳动物靶标的激活增加;但SESN2表达随EAA或AA供应增加而降低。过表达或抑制SESN2证明细胞增殖,酪蛋白表达和mTORC1途径的激活均受SESN2表达控制。此外,过表达SESN2抑制了细胞增殖,酪蛋白表达和响应于AA供应的mTORC1途径的激活,而通过抑制SESN2则逆转了这些作用。这些结果表明SESN2是CMEC中mTORC1的重要抑制剂,可阻止AA介导的细胞增殖和酪蛋白合成。

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