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大鼠视网膜中GTP结合蛋白Gi和G(o)的个体发生

Ontogeny of GTP-binding proteins, Gi and G(o), in rat retina.

作者信息

Oguni M, Shinohara H, Asano T, Kato K, Setogawa T

机构信息

Department of Ophthalmology, Shimane Medical University, Japan.

出版信息

Histochem Cell Biol. 1996 Aug;106(2):235-40. doi: 10.1007/BF02484406.

Abstract

The distribution and the levels of Gi1 (plus Gi3), Gi2, and G(o) in rat retina were studied immunohistochemically and immunochemically during development. At embryonic day (E) 15, Gi1 alpha/Gi3 alpha was observed in the inner layer of the neural retina, the future nerve fiber layer (NFL), while Gi2 alpha was observed both in the inner and outer layers of the neural retina. No immunoreactivity for G(o) alpha was observed. At E18, Gi1 alpha/Gi3 alpha and Gi2 alpha appeared in the inner plexiform layer (IPL), while G(o) alpha was faintly immunoreactive only in the NFL. At birth, Gi2 alpha/Gi3 alpha and G(o) alpha appeared in the ganglion cell layer. Gi2 alpha was intensely immunoreactive in the NFL and IPL. At postnatal day (P) 10, the inner portions of the retina, from the NFL to the outer plexiform layer, were immunoreactive to Gi1 alpha/Gi3 alpha, Gi2 alpha, and G(o) alpha. Gi1 alpha/Gi3 alpha and G(o) alpha were distributed characteristically in a laminated pattern in the IPL, but Gi2 alpha was present homogeneously in the IPL. At P12, Gi2 alpha appeared in the outer nuclear layer. As the postnatal days advanced, the laminated pattern of immunoreactivity to G(o) alpha in the IPL became diffuse, but immunoreactivity to Gi1 alpha/Gi3 alpha remained. The results of enzyme immunoassays showed that the concentration of G(o) alpha increased rapidly from P10 to P15 and reached almost the adult level at P20-P30, while Gi2 alpha decreased until P15 and was almost constant thereafter. These results showed that the distribution of Gi1 alpha/Gi3 alpha, Gi2 alpha, and G(o) alpha differs during development, suggesting that each G protein in the developing retina has a unique function.

摘要

在发育过程中,采用免疫组织化学和免疫化学方法研究了大鼠视网膜中Gi1(加Gi3)、Gi2和G(o)的分布及水平。胚胎第15天(E15)时,在神经视网膜的内层,即未来的神经纤维层(NFL)中观察到Gi1α/Gi3α,而在神经视网膜的内层和外层均观察到Gi2α。未观察到G(o)α的免疫反应性。E18时,Gi1α/Gi3α和Gi2α出现在内网层(IPL),而G(o)α仅在NFL中有微弱的免疫反应性。出生时,Gi2α/Gi3α和G(o)α出现在神经节细胞层。Gi2α在NFL和IPL中具有强烈的免疫反应性。出生后第10天(P10),视网膜从NFL到外网层的内部对Gi1α/Gi3α、Gi2α和G(o)α均有免疫反应性。Gi1α/Gi3α和G(o)α在IPL中呈特征性的分层分布模式,但Gi2α在IPL中均匀分布。P12时,Gi2α出现在外核层。随着出生后天数增加,IPL中对G(o)α的免疫反应性分层模式变得弥散,但对Gi1α/Gi3α的免疫反应性依然存在。酶免疫分析结果显示,G(o)α的浓度从P10到P15迅速增加,并在P20 - P30达到几乎成年水平,而Gi2α在P15之前下降,此后几乎保持恒定。这些结果表明,Gi1α/Gi3α、Gi2α和G(o)α在发育过程中的分布不同,提示发育中的视网膜中每种G蛋白具有独特功能。

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