Feinstein Yael, Klar Avihu
Department of Anatomy and Cell Biology, Hadassah Medical School, Hebrew University, P.O. Box 12272, Jerusalem 91120, Israel.
Int J Biochem Cell Biol. 2004 Jun;36(6):975-80. doi: 10.1016/j.biocel.2004.01.002.
F-spondin and Mindin are members of a subgroup of the thrombospondin type 1 (TSR) class molecules, defined by two domains of homology, the FS1/FS2 and TSR domains. The TSRs of F-spondin proteins are typical of class 2 TSRs. F-spondin and Mindin are evolutionarily conserved proteins. The embryonic expression of the vertebrate genes is enriched in the nervous system, mainly at the floor plate and the hippocampus. Similar to thrombospondin, F-spondin and Mindin are extracellular matrix attached molecules that promote neurite outgrowth and inhibit angiogenesis. Analysis of gain and loss of function experiments reveal that F-spondin is required for accurate pathfinding of embryonic axons. F-spondin plays a dual role in patterning axonal trajectories: it promotes the outgrowth of commissural and inhibits the outgrowth of motor axons. Macrophages of Mindin-deficient mice exhibit defective responses to a broad spectrum of microbial stimuli. This may implicate Mindin and F-spondin in inflammatory processes in the nervous system.
F-腱蛋白和Mindin是血小板反应蛋白1型(TSR)类分子亚组的成员,由两个同源结构域FS1/FS2和TSR结构域定义。F-腱蛋白的TSR属于典型的2类TSR。F-腱蛋白和Mindin是进化上保守的蛋白质。脊椎动物基因的胚胎表达在神经系统中富集,主要在底板和海马体。与血小板反应蛋白类似,F-腱蛋白和Mindin是附着于细胞外基质的分子,可促进神经突生长并抑制血管生成。功能获得和丧失实验分析表明,F-腱蛋白是胚胎轴突精确寻路所必需的。F-腱蛋白在轴突轨迹形成中起双重作用:它促进连合轴突的生长并抑制运动轴突的生长。Mindin缺陷小鼠的巨噬细胞对多种微生物刺激表现出缺陷反应。这可能表明Mindin和F-腱蛋白参与神经系统的炎症过程。