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Reggie-1和Reggie-2是视网膜神经节细胞在轴突再生过程中表达的两种细胞表面蛋白。

Reggie-1 and reggie-2, two cell surface proteins expressed by retinal ganglion cells during axon regeneration.

作者信息

Schulte T, Paschke K A, Laessing U, Lottspeich F, Stuermer C A

机构信息

Faculty of Biology, University of Konstanz, Germany.

出版信息

Development. 1997 Jan;124(2):577-87. doi: 10.1242/dev.124.2.577.

Abstract

Fish--in contrast to mammals--regenerate retinal ganglion cell axons when the optic nerve is severed. Optic nerve injury leads to reexpression of proteins, which typically are first expressed in newly differentiated retinal ganglion cells and axons. Here we identified two new proteins of fish retinal ganglion cells, reggie-1 and reggie-2, with monoclonal antibody M802 and molecular cloning techniques. In normal fish, M802 stained the few retinal axons derived from newborn ganglion cells which in fish are added lifelong to the retinal margin. After optic nerve injury, however, M802 labeled all retinal ganglion cells and retinal axons throughout their path into tectum. Consistent with M802 staining, reggie-1 and reggie-2 mRNAs were present in lesioned retinal ganglion cells, as demonstrated by in situ hybridization, but were not detectable in their normal mature counterparts. In western blots with membrane proteins of the adult goldfish brain, M802 recognizes a 48x10(3) Mr protein band. At the amino acid level, 48x10(3) Mr reggie-1 and reggie-2 are 44% identical, lack transmembrane and membrane anchor domains, but appear membrane associated by ionic interactions. Reggie-1 and reggie-2 are homologous to 35x10(3) Mr ESA (human epidermal surface antigen) but are here identified as neuronal surface proteins, present on newly differentiated ganglion cells at the retinal margin and which are reexpressed in mature ganglion cells upon injury and during axonal regeneration.

摘要

与哺乳动物不同,鱼类在视神经切断后能再生视网膜神经节细胞轴突。视神经损伤会导致蛋白质重新表达,这些蛋白质通常最初在新分化的视网膜神经节细胞和轴突中表达。在这里,我们用单克隆抗体M802和分子克隆技术鉴定了鱼类视网膜神经节细胞的两种新蛋白质,即reggie-1和reggie-2。在正常鱼类中,M802标记了源自新生神经节细胞的少数视网膜轴突,在鱼类中这些轴突终生添加到视网膜边缘。然而,视神经损伤后,M802标记了所有视网膜神经节细胞及其进入顶盖的整个路径中的视网膜轴突。与M802染色一致,原位杂交显示reggie-1和reggie-2 mRNA存在于受损的视网膜神经节细胞中,但在其正常成熟对应物中未检测到。在成年金鱼脑的膜蛋白免疫印迹中,M802识别出一条48×10³ Mr的蛋白带。在氨基酸水平上,48×10³ Mr的reggie-1和reggie-2有44%的同一性,缺乏跨膜和膜锚定结构域,但似乎通过离子相互作用与膜相关。Reggie-1和reggie-2与35×10³ Mr的ESA(人表皮表面抗原)同源,但在这里被鉴定为神经元表面蛋白,存在于视网膜边缘新分化的神经节细胞上,并且在损伤后和轴突再生期间在成熟神经节细胞中重新表达。

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