Pickard Bryce, Damjanovski Sashko
Department of Biology, University of Western Ontario, London, Ontario, Canada.
Cell Res. 2004 Oct;14(5):389-99. doi: 10.1038/sj.cr.7290239.
Tissue inhibitors of metalloproteinases (TIMPs) modulate extracellular matrix remodeling during embryonic development and disease. TIMP-3 expression was examined during Xenopus laevis embryogenesis: TIMP-3 transcripts detected in the maternal pool of RNA increased at the mid-blastula transition, decreased dramatically during gastrulation and increased again during neurulation and axis elongation. Interestingly, the decrease during gastrulation was not seen in LiCl treated (dorsalized) embryos. Whole mount in situ hybridization of TIMP-3 using DIG-labeled RNA probes demonstrated that the transcripts were present in all dorsal tissues during embryogenesis, but were prominent only in head structures starting at stage 35. Overexpression of TIMP-3 through transgenesis and RNA injections led to developmental abnormalities and death. Both overexpression strategies resulted in post-gastrulation perturbation including those to neural and head structures, as well as truncated axes. However, RNA injections resulted in more severe early defects such as failure of neural tube closure, and transgenesis caused truncated axes and head abnormalities. No transgenic embryo expressing TIMP-3 survived past stage 40.
金属蛋白酶组织抑制剂(TIMPs)在胚胎发育和疾病过程中调节细胞外基质重塑。在非洲爪蟾胚胎发生过程中检测了TIMP-3的表达:在RNA的母源池中检测到的TIMP-3转录本在囊胚中期转变时增加,在原肠胚形成期间急剧下降,在神经胚形成和轴伸长期间再次增加。有趣的是,在氯化锂处理(背化)的胚胎中未观察到原肠胚形成期间的下降。使用地高辛标记的RNA探针进行TIMP-3的全胚胎原位杂交表明,转录本在胚胎发生期间存在于所有背侧组织中,但仅在第35阶段开始时在头部结构中突出。通过转基因和RNA注射过表达TIMP-3导致发育异常和死亡。两种过表达策略都导致原肠胚形成后扰动,包括对神经和头部结构的扰动,以及轴缩短。然而,RNA注射导致更严重的早期缺陷,如神经管闭合失败,而转基因导致轴缩短和头部异常。没有表达TIMP-3的转基因胚胎能存活到第40阶段以后。