Sieber-Blum M, Zhang J M
Department of Cellular Biology and Anatomy, Medical College of Wisconsin, Milwaukee 53226, USA.
J Anat. 1997 Nov;191 ( Pt 4)(Pt 4):493-9. doi: 10.1046/j.1469-7580.1997.19140493.x.
At the onset of their migration into the embryo, many neural crest cells are pluripotent in the sense that they have the capacity to generate progeny that consist of more than one cell type. More recently, we have found that there are pluripotent neural crest cell-derived cells even at sites of terminal differentiation. These findings support the notion that cues originating from the microenvironment, at least in part, direct neural crest cell type specification. Based on the rationale that growth factors that are known to support survival of neural crest cell derivatives may have additional functions in progenitor cell development, we have examined the action of pertinent growth factors. Trophic, mitogenic, antiproliferative and differentiation promoting activities were found. Stem cell factor (SCF) is trophic for pluripotent neural crest cells. Contrary to expectation, SCF plus a neurotrophin, rather than SCF alone is trophic for committed melanogenic cells. Basic fibroblast growth factor (bFGF) is mitogenic both for pluripotent cells and committed melanogenic cells. However, the cells become dependent on another factor for survival. Whereas any neurotrophin tested can rescue bFGF-activated pluripotent neural crest cells, the factor that rescues melanogenic cells remains to be determined. Transforming growth factor beta 1 (TGF-beta 1) is a powerful antimitotic signal for all neural crest cells that overrides the bFGF/neurotrophin proliferative signal. Furthermore, SCF promotes differentiation of neural crest cells into cells of the sensory neuron lineage. Neurotrophin-3 (NT-3) specifically promotes high affinity uptake of norepinephrine by neural crest cells and is thus thought to play a critical role in the differentiation of sympathetic neuroblasts. In summary, our data indicate that neurotrophins and other pertinent growth factors affect survival, proliferation and differentiation of neural crest cells at multiple levels and in different lineages. Moreover, our findings emphasise the importance of the concerted action of combinations of growth factors, rather than of individual factors.
在迁移进入胚胎时,许多神经嵴细胞具有多能性,因为它们有能力产生由不止一种细胞类型组成的后代。最近,我们发现即使在终末分化部位也存在多能性神经嵴细胞衍生的细胞。这些发现支持了这样一种观点,即至少部分源自微环境的信号指导神经嵴细胞类型的特化。基于已知支持神经嵴细胞衍生物存活的生长因子可能在祖细胞发育中具有额外功能这一原理,我们研究了相关生长因子的作用。发现了营养、促有丝分裂、抗增殖和促进分化的活性。干细胞因子(SCF)对多能性神经嵴细胞具有营养作用。与预期相反,SCF加上一种神经营养因子,而不是单独的SCF,对已定向的黑素生成细胞具有营养作用。碱性成纤维细胞生长因子(bFGF)对多能细胞和已定向的黑素生成细胞都有促有丝分裂作用。然而,这些细胞变得依赖另一种因子来存活。虽然所测试的任何一种神经营养因子都能挽救bFGF激活的多能性神经嵴细胞,但挽救黑素生成细胞的因子仍有待确定。转化生长因子β1(TGF-β1)是所有神经嵴细胞的强大抗有丝分裂信号,它能超越bFGF/神经营养因子的增殖信号。此外,SCF促进神经嵴细胞分化为感觉神经元谱系的细胞。神经营养因子-3(NT-3)特异性促进神经嵴细胞对去甲肾上腺素的高亲和力摄取,因此被认为在交感神经母细胞的分化中起关键作用。总之,我们的数据表明神经营养因子和其他相关生长因子在多个水平和不同谱系中影响神经嵴细胞的存活、增殖和分化。此外,我们的发现强调了生长因子组合协同作用而非单个因子作用的重要性。