SUN1 inhibits osteogenesis and promotes adipogenesis of human adipose-derived stem cells by regulating α-tubulin and CD36 expression

J Cell Mol Med. 2024 Oct;28(19):e70143. doi: 10.1111/jcmm.70143.

Abstract

Sad and UNC84 domain 1 (SUN1) is a kind of nuclear envelope protein with established involvement in cellular processes, including nuclear motility and meiosis. SUN1 plays an intriguing role in human adipose-derived stem cells (hASCs) differentiation; however, this role remains largely undefined. This study was undertaken to investigate the role of SUN1 in hASCs differentiation, as well as its underlying mechanisms. Employing siRNAs, we selectively downregulated SUN1 and CD36 expression. Microtubules were depolymerized using nocodazole, and PPARγ was activated using rosiglitazone. Western blotting was performed to quantify SUN1, PPARγ, α-tubulin, CD36, OPN, and adiponectin protein expression levels. Alkaline phosphatase and Oil red O staining were used to assess osteogenesis and adipogenesis, respectively. Downregulated SUN1 expression increased osteogenesis and decreased adipogenesis in hASCs, concomitant with upregulated α-tubulin expression and downregulated CD36 expression, alongside reduced nuclear localization of PPARγ. Microtubule depolymerization increased CD36 expression. Rescue experiments indicated that microtubule depolymerization counteracted the downregulated SUN1-induced phenotypic changes. This study demonstrates that SUN1 influences the differentiation of hASCs towards osteogenic and adipogenic lineages, indicating its essential role in cell fate.

Keywords: CD36; Sad1 and UNC84 domain 1; adipogenesis; osteogenesis; α‐Tubulin.

MeSH terms

  • Adipogenesis* / genetics
  • Adipose Tissue* / cytology
  • Adipose Tissue* / metabolism
  • CD36 Antigens* / genetics
  • CD36 Antigens* / metabolism
  • Cell Differentiation*
  • Cells, Cultured
  • Gene Expression Regulation
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Nuclear Proteins
  • Osteogenesis* / genetics
  • PPAR gamma* / genetics
  • PPAR gamma* / metabolism
  • Stem Cells* / cytology
  • Stem Cells* / metabolism
  • Tubulin* / metabolism

Substances

  • CD36 Antigens
  • Tubulin
  • PPAR gamma
  • SUN1 protein, human
  • Membrane Proteins
  • Microtubule-Associated Proteins
  • CD36 protein, human
  • Nuclear Proteins