Chang Hua, Brown Chester W, Matzuk Martin M
Department of Pathology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.
Endocr Rev. 2002 Dec;23(6):787-823. doi: 10.1210/er.2002-0003.
Members of the TGF-beta superfamily, which includes TGF-betas, growth differentiation factors, bone morphogenetic proteins, activins, inhibins, and glial cell line-derived neurotrophic factor, are synthesized as prepropeptide precursors and then processed and secreted as homodimers or heterodimers. Most ligands of the family signal through transmembrane serine/threonine kinase receptors and SMAD proteins to regulate cellular functions. Many studies have reported the characterization of knockout and knock-in transgenic mice as well as humans or other mammals with naturally occurring genetic mutations in superfamily members or their regulatory proteins. These investigations have revealed that TGF-beta superfamily ligands, receptors, SMADs, and upstream and downstream regulators function in diverse developmental and physiological pathways. This review attempts to collate and integrate the extensive body of in vivo mammalian studies produced over the last decade.
转化生长因子-β(TGF-β)超家族成员包括TGF-β、生长分化因子、骨形态发生蛋白、激活素、抑制素和胶质细胞源性神经营养因子,它们最初作为前体肽前体被合成,然后加工并以同二聚体或异二聚体形式分泌。该家族的大多数配体通过跨膜丝氨酸/苏氨酸激酶受体和SMAD蛋白发出信号,以调节细胞功能。许多研究报道了基因敲除和基因敲入转基因小鼠以及在超家族成员或其调节蛋白中存在自然发生基因突变的人类或其他哺乳动物的特征。这些研究表明,TGF-β超家族配体、受体、SMAD蛋白以及上游和下游调节因子在多种发育和生理途径中发挥作用。本综述试图整理和整合过去十年中产生的大量体内哺乳动物研究。