Bernfield M, Hinkes M T, Gallo R L
Joint Program in Neonatology, Harvard Medical School, Boston, MA 02115.
Dev Suppl. 1993:205-12.
Recent work has made clear that heparan sulfate at the cell surface is essential for a wide variety of interactions of cells with their microenvironment, including the action of growth factors, extracellular matrix, proteases and protease inhibitors. A major source of this cell surface heparan sulfate is a multigene family of proteoglycans, the syndecans, that are expressed developmentally in association with changes in tissue organization and morphology and induced during wound repair. In this review, we describe mechanisms underlying the differential expression of the syndecans, focusing on syndecan-1. The induction of syndecan-1 can result from soluble extracellular factor(s) acting at multiple levels of cellular regulation. At the transcriptional level, the promoter of the murine syndecan-1 gene contains potential recognition sites for several well-known regulatory genes, including Hox and MyoD family members. Because changes in syndecan expression enable cells to become more or less responsive to their microenvironment, understanding these regulatory mechanisms can lead to an improved understanding of how cellular behavior is controlled during development and wound repair.
最近的研究表明,细胞表面的硫酸乙酰肝素对于细胞与其微环境的多种相互作用至关重要,包括生长因子、细胞外基质、蛋白酶和蛋白酶抑制剂的作用。这种细胞表面硫酸乙酰肝素的主要来源是一个蛋白聚糖多基因家族,即syndecans,它们在发育过程中与组织组织和形态的变化相关表达,并在伤口修复过程中被诱导。在这篇综述中,我们描述了syndecans差异表达的潜在机制,重点是syndecan-1。syndecan-1的诱导可能是由可溶性细胞外因子在细胞调节的多个水平上起作用导致的。在转录水平上,小鼠syndecan-1基因的启动子包含几个著名调节基因的潜在识别位点,包括Hox和MyoD家族成员。由于syndecan表达的变化使细胞对其微环境的反应或多或少,了解这些调节机制可以更好地理解细胞行为在发育和伤口修复过程中是如何被控制的。