BMPs, TGFbetas and integrins in muscle and germ cell development in mice

Abstract

We characterized the expression of PSmad1/5/8 (BMP R-Smads) and PSmad2 (TGFbeta R-Smad) during peri-implantation and gastrulation in the mouse, and further characterized the expression of PSmad2 until E12.5, showing were the BMP and TGFbeta Smad-dependent signalling pathways are active (Chapter 2, 3 and 4).

The role of ALK2 (BMP signalling) and ALK5 (TGFbeta signalling) in the development of PGCs in the mouse was studied in detail. ALK2 is needed for the formation of PGCs before gastrulation occurs and it signals in the visceral endoderm, a tissue that was previously not associated with primordial germ cell formation (Chapter 3). In contrast to suggestions derived from studies in vitro, ALK5 is probably not involved in PGC migration through the hindgut and to the gonadal ridges and TGF 1 is unlikely to be a chemoattractant for PGCs as proposed (Chapter 4). However, there may be a role for TGF signalling in PGC development in controlling mitotic arrest of PGCs in the gonadal ridges.

Beta1 integrin was also implicated in PGC migration to the genital ridges. Beta1 integrin has two isoforms in mice: a more common one beta1A and a muscle specific beta1D that is upregulated late during development. We studied whether the replacement of beta1A by beta1D influenced the development of PGCs, but this occurred normally and we found no evidence of an effect on migration on the genetic background used. Furthermore, beta1 integrin has been implicated in heart development. We showed that the replacement of beta1A by beta1D did not cause heart abnormalities during development. However, we were able to show a clear role for beta1A during myogenesis. The differentiation of primary myoblasts was abnormal when only beta1D was expressed, while secondary myoblasts were formed normally. Furthermore, we showed a novel role of beta1 integrin during placentation, in particular the development of the labyrinthine layer (Chapter 5).

CTGF is known to crosstalk with both TGFbeta and BMP in vitro. We studied possible interactions between them, focusing on heart development, where BMP and TGFbeta are known to play prominent roles. However, we were not able to detect direct crosstalk. Both CTGF and TGFbeta are associated with fibrosis. We investigated whether CTGF and TGFbeta were expressed following experimental induction of myocardial infarction in the mouse and showed that both genes are present in particular in the scar tissue and that TGFbeta Smad-dependent signalling is transient 1 week post-infarction and largely restricted to cardiac fibroblasts (Chapter 6).