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Extracellular Glutamine Promotes Intestinal Porcine Epithelial Cell Proliferation via Arf1-mTORC1 Pathway Independently of Rag GTPases.
Yan, Ling; Fang, Yong-Xia; Lu, En-Qing; Xu, E; Zhang, Yi-Yu; Chen, Xiang; Zhu, Min.
Afiliación
  • Yan L; Laboratory of Animal Genetics, Breeding and Reproduction in the Plateau Mountainous Region, Ministry of Education, College of Animal Science, Guizhou University, Guiyang 550025, Guizhou Province China.
  • Fang YX; Institute of Animal Nutrition and Feed Science, Guizhou University, Guiyang 550025, China.
  • Lu EQ; Laboratory of Animal Genetics, Breeding and Reproduction in the Plateau Mountainous Region, Ministry of Education, College of Animal Science, Guizhou University, Guiyang 550025, Guizhou Province China.
  • Xu E; Institute of Animal Nutrition and Feed Science, Guizhou University, Guiyang 550025, China.
  • Zhang YY; Laboratory of Animal Genetics, Breeding and Reproduction in the Plateau Mountainous Region, Ministry of Education, College of Animal Science, Guizhou University, Guiyang 550025, Guizhou Province China.
  • Chen X; Institute of Animal Nutrition and Feed Science, Guizhou University, Guiyang 550025, China.
  • Zhu M; Laboratory of Animal Genetics, Breeding and Reproduction in the Plateau Mountainous Region, Ministry of Education, College of Animal Science, Guizhou University, Guiyang 550025, Guizhou Province China.
J Agric Food Chem ; 71(39): 14251-14262, 2023 Oct 04.
Article en En | MEDLINE | ID: mdl-37738360
Glutamine (Gln) is the major energy source of intestinal porcine epithelial cells (IPEC-J2 cells) and plays a critical role in the nutritional physiological function of the intestine. However, the underlying mechanism requires further investigation. Here, the Gln-sensing pathway in IPEC-J2 cells was investigated. The results showed that Gln increased the cell proliferation. Subsequently, an analysis of the phosphorylated proteome revealed that Gln markedly upregulated ribosomal protein S6 (RPS6) phosphorylation at serine 235/236, suggesting that Gln activated the mTORC1 pathway. mTOR inhibition revealed that Gln promotes cell proliferation through the mTORC1 pathway. Similarly, blocking ADP-ribosylation factor 1 (Arf1) activity indicated that Gln-induced mTORC1 activation promoted cell proliferation in an Arf1-dependent manner. Additionally, the RagA/B pathway did not participate in Gln-induced mTORC1 activation. Collectively, these findings suggest that Gln-induced mTORC1 activation promotes IPEC-J2 cell proliferation via Arf1, not Rag GTPases. These results broaden our understanding of functional-cell-sensing amino acids, particularly Gln, that are regulated by mTORC1.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factor 1 de Ribosilacion-ADP / Glutamina Idioma: En Revista: J Agric Food Chem Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factor 1 de Ribosilacion-ADP / Glutamina Idioma: En Revista: J Agric Food Chem Año: 2023 Tipo del documento: Article