Differential expression of FGF receptors and of myogenic regulatory factors in primary cultures of satellite cells originating from fast (EDL) and slow (Soleus) twitch rat muscles
I. Martelly et al., Differential expression of FGF receptors and of myogenic regulatory factors in primary cultures of satellite cells originating from fast (EDL) and slow (Soleus) twitch rat muscles, CELL MOL B, 46(7), 2000, pp. 1239-1248
In the rat, the fast and slow twitch muscles respectively Extensor digitoru
m longus (EDL) and Soleus present differential characteristics during regen
eration. This suggests that their satellite cells responsible for muscle gr
owth and repair represent distinct cellular populations. We have previously
shown that satellite cells dissociated from Soleus and grown in vitro prol
iferate more readily than those isolated from EDL muscle. Fibroblast growth
factors (FGFs) are known as regulators of myoblast proliferation and sever
al studies have revealed a relationship between the response of myoblasts t
o FGF and the expression of myogenic regulatory factors (MRF) of the MyoD f
amily by myoblasts. Therefore, we presently examined the possibility that t
he satellite cells isolated from EDL and Soleus muscles differ in the expre
ssion of FGF receptors (FGR-R) and of MRF expression. FGF-R1 and -R4 were s
trongly expressed in proliferating cultures whereas FGF-R2 and R3 were not
detected in these cultures. In differentiating cultures, only -R1 was prese
nt in EDL satellite cells while FGF-R4 was also still expressed in Soleus c
ells, interestingly, the unconventional receptor for FGF called cystein ric
h FGF receptor (CFR), of yet unknown function, was mainly detected in EDL s
atellite cell cultures. Soleus and EDL satellite cell cultures also differe
d in the expression MRFs. These results are consistent with the notion that
satellite cells from fast and slow twitch muscles belong to different type
s of myogenic cells and suggest that satellite cells might play distinct ro
les in the formation and diversification of fast and slow fibres.