Reduction of peritoneal cavity B1a cells in adult Slc7a5 knockdown mice via dysregulating the mTOR pathway

Int Immunopharmacol. 2023 Apr:117:109939. doi: 10.1016/j.intimp.2023.109939. Epub 2023 Mar 10.

Abstract

Slc7a5 is an important amino acid transporter that is highly expressed in metabolically active and rapidly proliferating cells. To explore the effect of Slc7a5 on adult B cell development, we conditionally deleted Slc7a5 in murine B cells and observed a significant reduction of B1a cells. In contrast to PI3K-Akt pathway activation, activity of the mTOR pathway was decreased. This may result from intracellular amino acid starvation in Slc7a5 knockdown (Slc7a5 KD) bone marrow B cells, thereby dampening B1a development. RNA-seq analysis demonstrated increased translation and reduced proliferation in Slc7a5 KD bone marrow B cells. Overall, the results of our study highlight the importance of Slc7a5 in peritoneal B1a cell development.

Keywords: B1a cell; Peritoneal cavity; Slc7a5; mTOR pathway.

MeSH terms

  • Animals
  • B-Lymphocytes* / metabolism
  • Cell Proliferation
  • Large Neutral Amino Acid-Transporter 1* / genetics
  • Large Neutral Amino Acid-Transporter 1* / metabolism
  • Mice
  • Peritoneal Cavity*
  • Phosphatidylinositol 3-Kinases / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Large Neutral Amino Acid-Transporter 1
  • Phosphatidylinositol 3-Kinases
  • TOR Serine-Threonine Kinases
  • Slc7a5 protein, mouse