I. Goddard et al., TRANSFORMING GROWTH-FACTOR-BETA RECEPTOR EXPRESSION IN CULTURED PORCINE GRANULOSA-CELLS, Molecular and cellular endocrinology, 115(2), 1995, pp. 207-213
By using primary cultures of porcine granulosa cells as a model, TGF b
eta receptors have been identified and characterized through three dif
ferent approaches including cross-linking experiments, Western- and No
rthern-blotting analysis. In cross-linking experiments, labeled TGF be
ta was shown to bind to four different molecular species of 300, 168,
72 and 58 kDa. The 300-kDa species may correspond to beta-glycan, whil
e the 72- and 58-kDa correspond to TGF beta type II and I receptors, r
espectively. The presence of these receptors was further demonstrated
by Western blotting analysis using specific polyclonal antibodies. Fin
ally, both the expression of beta-glycan, type II and type I mRNA, was
confirmed through Northern-blotting analysis as shown by the presence
of 6.4, 4.6 and 5.8 kb mRNA, respectively. Additionally, we detected
another TGF beta binding protein of 168 kDa which remains to be identi
fied. Together, our present data indicate that the regulatory action o
f TGF beta on cultured granulosa cells previously reported in several
laboratories may be mediated through the receptors identified here.