Britto Joanne M, Lukehurst Sherralee, Weller Renae, Fraser Chris, Qiu Yubin, Hertzog Paul, Busfield Samantha J
Western Australian Institute for Medical Research and UWA Centre for Medical Research, University of Western Australia, Perth, Australia.
Mol Cell Biol. 2004 Sep;24(18):8221-6. doi: 10.1128/MCB.24.18.8221-8226.2004.
The neuregulins (NRGs) are a family of four structurally related growth factors that are expressed in the developing and adult brain. NRG-1 is essential for normal heart formation and has been implicated in the development and maintenance of both neurons and glia. NRG-2 was identified on the basis of its homology to NRG-1 and, like NRG-1, is expressed predominantly by neurons in the central nervous system. We have generated mice with the active domain of NRG-2 deleted in an effort to characterize the biological function of NRG-2 in vivo. In contrast to the NRG-1 knockout animals, NRG-2 knockouts have no apparent heart defects and survive embryogenesis. Mutant mice display early growth retardation and reduced reproductive capacity. No obvious histological differences were observed in the major sites of NRG-2 expression. Our results indicate that in vivo NRG-2 activity differs substantially from that of NRG-1 and that it is not essential for normal development in utero.
神经调节蛋白(NRGs)是一族由四种结构相关的生长因子组成的蛋白,在发育中的大脑和成年大脑中均有表达。NRG-1对正常心脏形成至关重要,并且与神经元和神经胶质细胞的发育及维持有关。NRG-2是基于其与NRG-1的同源性而被鉴定出来的,与NRG-1一样,主要由中枢神经系统中的神经元表达。为了在体内表征NRG-2的生物学功能,我们构建了缺失NRG-2活性结构域的小鼠。与NRG-1基因敲除动物不同,NRG-2基因敲除小鼠没有明显的心脏缺陷,并且能够存活至胚胎发育完成。突变小鼠表现出早期生长发育迟缓以及繁殖能力下降。在NRG-2表达的主要部位未观察到明显的组织学差异。我们的结果表明,在体内NRG-2的活性与NRG-1的活性有很大不同,并且它对于子宫内的正常发育并非必不可少。