TRANSFORMING GROWTH-FACTOR-BETA ALTERS DIFFERENTIATION IN CULTURES OF AVIAN NEURAL CREST-DERIVED CELLS - EFFECTS ON CELL MORPHOLOGY, PROLIFERATION, FIBRONECTIN EXPRESSION, AND MELANOGENESIS

Neural crest cell differentiation is responsive to a variety of extrinsic signals that include extracellular matrix (ECM) molecules and growth factors. Transforming growth factor-β (TGF-β) has diverse, cell type-specific effects, many of which involve regulation of synthesis of ECM molecules and their cell surface receptors. We are studying both separate and potentially interrelated influences of ECM and growth factors on crest differentiation and report here that TGF-β alters several aspects of crest cell behavior in vitro. Clusters of quail neural crest cells were cultured in the presence and absence of 400 pM TGF-β1 and examined at 1, 3, and 5 days. When examined at 5 days, there was a dramatic decrease in the number of melanocytes in treated cultures, regardless of the onset or duration of TGF-β treatment. With continuous TGF-β treatment, or with treatment only during crest cluster formation on explanted neural tubes, many cells increased in area, becoming extremely flat. These changes were evident beginning on Day 3. While quantitative analyses of video images documented the size increase, several aspects of motility were relatively unchanged. Synthesis of fibronectin (FN) by approximately 11% of cells on Day 3 and 31% of cells on Day 5 was demonstrated by immunocytochemistry and was associated with a sixfold increase in FN mRNA by Day 5. Experiments which correlated FN immunoreactivity with incorporation of bromodeoxyuridine suggested that the population of large, flat, FN-positive cells did not proliferate selectively and that there was a slower rate of proliferation in TGF-β-treated cultures than in untreated cultures. The large FN-immunoreactive cells resemble cells derived from cepalic neural crest and raise interesting questions concerning potential roles for TGF-β in regulating crest differentiation in vivo. © 1992.