Growth factors in mouse primordial germ cell migration and proliferation

Massimo De Felici, Maurizio Pesce
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引用次数: 51

Abstract

Information obtained mainly from in vitro culture studies and genetic analysis of mouse mutants White spotting and Steel indicate a pivotal role of growth factors in the development of mouse primordial germ cells (PGCs). While stem cell factor (SCF) and TGFβ1 seem to have a role in PGC migration (as an adhesion factor and a chemoattractant, respectively), the former is certainly required for PGC survival in vitro and probably in vivo as well. Recent findings suggest that the mechanism by which SCF supports PGC survival is by preventing PGC apoptosis. A similar action appears to be exerted by leukemia inhibitory factor (LIF), a further growth factor influencing PGC growth in culture.

PGC proliferation seems to be mainly induced by cAMP dependent mechanisms, but futther investigations are needed to clarify the interrelationships among the different molecular pathways activated by SCF, LIF, cAMP and other putative PGC growth factors (i.e. bFGF). Stimulation of long-term proliferation of PGCs, leading to derivation of ES-like cells (embryonal germ cells) obtained by using a combination of growth factors (bFGF, SCF and LIF), opens new intriguing perspectives for such studies and transgenic technology.

生长因子对小鼠原始生殖细胞迁移和增殖的影响
主要从小鼠突变体White spotting和Steel的体外培养研究和遗传分析中获得的信息表明,生长因子在小鼠原始生殖细胞(PGCs)的发育中起着关键作用。虽然干细胞因子(SCF)和TGFβ1似乎在PGC迁移中发挥作用(分别作为粘附因子和趋化剂),但前者肯定是PGC在体外和体内存活所必需的。最近的研究结果表明,SCF支持PGC存活的机制是通过阻止PGC凋亡。白血病抑制因子(LIF)似乎也有类似的作用,LIF是影响PGC生长的另一个生长因子。PGC增殖似乎主要由cAMP依赖机制诱导,但SCF、LIF、cAMP和其他可能的PGC生长因子(如bFGF)激活的不同分子通路之间的相互关系需要进一步研究。通过使用生长因子(bFGF, SCF和LIF)的组合,刺激PGCs的长期增殖,导致es样细胞(胚胎生殖细胞)的衍生,为此类研究和转基因技术开辟了新的有趣的前景。
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