SGLT2 knockdown restores the Th17/Treg balance and suppresses diabetic nephropathy in db/db mice by regulating SGK1 via Na

Mol Cell Endocrinol. 2024 Apr 15:584:112156. doi: 10.1016/j.mce.2024.112156. Epub 2024 Jan 24.

Abstract

The imbalance between T helper 17 (Th17) and regulatory T (Treg) cells is an important mechanism in the pathogenesis of diabetic nephropathy (DN). Serum/glucocorticoid regulated kinase 1 (SGK1) is a serine-threonine kinase critical for stabilizing the Th17 cell phenotype. Sodium-glucose cotransporter 2 (SGLT2) is a glucose transporter that serves as a treatment target for diabetes. Our study investigated the regulatory role of SGLT2 in the development of DN. The results revealed that SGLT2 knockdown suppressed high glucose-induced excessive secretion of sodium (Na+) and inflammatory cytokines in mouse renal tubular epithelial TCMK-1 cells. High Na+ content induced Th17 differentiation and upregulated SGK1, phosphorylated forkhead box protein O1 (p-FoxO1), and the interleukin 23 receptor (IL-23 R) in primary mouse CD4+ T cells. Co-culture of CD4+ T cells with the culture medium of TCMK-1 cells with insufficient SGLT2 expression significantly suppressed cell migration ability, reduced the production of pro-inflammatory cytokines, and inhibited Th17 differentiation possibly by downregulating SGK1, p-FoxO1, and IL-23 R. In addition, in vivo data demonstrated that SGLT2 knockdown markedly downregulated SGK1 in db/db mice. Insufficient SGLT2 or SGK1 expression also ameliorated the Th17/Treg imbalance, suppressed the development of DN, and regulated the expression of IL-23 R and p-FoxO1. In conclusion, this study showed that SGLT2 knockdown restored the Th17/Treg balance and suppressed DN possibly by regulating the SGK1/p-FoxO1/IL-23 R axis by altering Na+ content in the local environment. These findings highlight the potential use of SGLT2 and SGK1 for the management of DN.

Keywords: Diabetic nephropathy; SGK1; SGLT2; Th17; Tregs.

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Diabetes Mellitus* / metabolism
  • Diabetic Nephropathies* / genetics
  • Diabetic Nephropathies* / metabolism
  • Glucocorticoids / metabolism
  • Glucose / metabolism
  • Immediate-Early Proteins* / metabolism
  • Interleukin-23 / metabolism
  • Mice
  • Mice, Inbred Strains
  • Protein Serine-Threonine Kinases* / metabolism
  • Sodium / metabolism
  • Sodium-Glucose Transporter 2* / metabolism
  • T-Lymphocytes, Regulatory

Substances

  • Cytokines
  • Glucocorticoids
  • Glucose
  • Interleukin-23
  • Sodium
  • Sodium-Glucose Transporter 2
  • Slc5a2 protein, mouse
  • serum-glucocorticoid regulated kinase
  • Protein Serine-Threonine Kinases
  • Immediate-Early Proteins