Altered primordial germ cell migration in the absence of transforming growth factor beta signaling via ALK5

S M C D Lopes, S van den Driesche, R L C Carvalho, Jonas Larsson, B Eggen, M A Surani, C L Mummery

Research output: Contribution to journalArticlepeer-review

46 Citations (SciVal)

Abstract

Transforming growth factor beta (TGF beta) inhibits proliferation and promotes the migration of primordial germ cells (PGCs) towards explants of gonadal ridges in vitro. However, its effects in vivo are still unclear. Here, we analyzed the behavior of PGCs in embryos lacking TGF beta signaling via the type I receptor ALK5. TGF beta in vivo was neither a chemoattractant for PGCs, nor did it affect their proliferation during migration towards the gonadal ridges up to embryonic day (E) 10. Unexpectedly, the absence of TGF beta signaling in fact resulted in significant facilitation of PGC migration out of the hindgut, due to the reduced deposition of collagen type I surrounding the gut of Alk5-deficient mutant embryos. Migratory PGCs adhere strongly to collagen; therefore, reduced collagen type I along the gut may result in reduced adhesion, facilitating migration into the dorsal mesenterium and gonadal ridges. Our results provide new evidence for the role of TGF beta signaling in migration of PGCs in vivo distinct from that described previously.
Original languageEnglish
Pages (from-to)194-203
JournalDevelopmental Biology
Volume284
Issue number1
DOIs
Publication statusPublished - 2005

Subject classification (UKÄ)

  • Hematology

Keywords

  • migration
  • TGF beta
  • primordial germ cells
  • mouse embryo
  • collagen
  • hindgut

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