PTBP1 mediates Sertoli cell actin cytoskeleton organization by regulating alternative splicing of actin regulators

Nucleic Acids Res. 2024 Nov 11;52(20):12244-12261. doi: 10.1093/nar/gkae862.

Abstract

Spermatogenesis is a biological process within the testis that produces haploid spermatozoa for the continuity of species. Sertoli cells are somatic cells in the seminiferous epithelium that orchestrate spermatogenesis. Cyclic reorganization of the Sertoli cell actin cytoskeleton is vital for spermatogenesis, but the underlying mechanism remains largely unclear. Here, we report that the RNA-binding protein PTBP1 controls Sertoli cell actin cytoskeleton reorganization by programming alternative splicing of actin cytoskeleton regulators. This splicing control enables ectoplasmic specializations, the actin-based adhesion junctions, to maintain the blood-testis barrier and support spermatid transport and transformation. Particularly, we show that PTBP1 promotes actin bundle formation by repressing the inclusion of exon 14 of Tnik, a kinase present at the ectoplasmic specialization. Our results thus reveal a novel mechanism wherein Sertoli cell actin cytoskeleton dynamics are controlled post-transcriptionally by utilizing functionally distinct isoforms of actin regulatory proteins, and PTBP1 is a critical regulatory factor in generating such isoforms.

MeSH terms

  • Actin Cytoskeleton* / genetics
  • Actin Cytoskeleton* / metabolism
  • Actins / genetics
  • Actins / metabolism
  • Alternative Splicing* / genetics
  • Animals
  • Blood-Testis Barrier / metabolism
  • Cofilin 1 / genetics
  • Cofilin 1 / metabolism
  • Exons / genetics
  • Heterogeneous-Nuclear Ribonucleoproteins* / genetics
  • Heterogeneous-Nuclear Ribonucleoproteins* / metabolism
  • Male
  • Mice
  • Polypyrimidine Tract-Binding Protein* / genetics
  • Polypyrimidine Tract-Binding Protein* / metabolism
  • Sertoli Cells* / metabolism
  • Spermatids / metabolism
  • Spermatogenesis / genetics

Substances

  • Polypyrimidine Tract-Binding Protein
  • Heterogeneous-Nuclear Ribonucleoproteins
  • Ptbp1 protein, mouse
  • Actins
  • Cofilin 1