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一种肌肉衍生的底物结合因子,可促进中枢和外周神经系统神经元的神经突生长。

A muscle-derived substrate-bound factor that promotes neurite outgrowth from neurons of the central and peripheral nervous systems.

作者信息

Oh T H, Markelonis G J, Dion T L, Hobbs S L

机构信息

Department of Anatomy, University of Maryland, School of Medicine, Baltimore 21201.

出版信息

Dev Biol. 1988 May;127(1):88-98. doi: 10.1016/0012-1606(88)90191-1.

Abstract

The development and survival of spinal motor neurons depends upon muscle-derived trophic factors. Some circumstantial evidence suggested to us that the regulatory subunit of cyclic adenosine 3':5'-monophosphate-dependent protein kinase (cAMP-dPK)-type II might be involved in neuritic outgrowth from spinal neurons. In the present study, we tested a commercial preparation of cAMP-dPK for neurite-promoting activity. Commercial cAMP-dPK-type II from skeletal and cardiac muscles elicited a significant neurite outgrowth from cultured embryonic chicken neurons when the enzyme preparation was bound to polylysine-coated substrata; type I cAMP-dPK from skeletal muscle was ineffective. Neither cAMP-dPK-type I nor -type II had a significant effect on the survival of spinal neurons in culture. Type II cAMP-dPK also stimulated neurite outgrowth from chicken cerebral hemisphere neurons, dorsal root ganglionic neurons, ciliary ganglionic neurons, and rat sympathetic ganglionic neurons in culture. The neurite-promoting activity appears to reside in a contaminant of the preparation since neither the purified regulatory nor catalytic subunits of cAMP-dPK-type II had an effect on neurite outgrowth per se from cultured neurons and since neurite-promoting activity did not correlate with [3H]cAMP binding or cAMP-dependent kinase activity. The neurite-promoting protein was then partially purified from commercial cAMP-dPK-type II by gel filtration on Sephadex G-200 followed by ion-exchange chromatography on DE-52 cellulose. Sodium dodecyl sulfate gel electrophoresis of the active protein peak revealed a major protein band (MW 50 kDa) and several minor bands (e.g., MW 200 kDa, 52 kDa, 45 kDa). Also, immunoblot analysis and immunoprecipitation revealed that the partially purified neurite-promoting protein was distinct from laminin, heparan sulfate proteoglycan, nerve growth factor, neural cell adhesion molecule, and fibronectin. Furthermore, the neurite-promoting activity was not diminished by treatment with heparinase nor was it bound to heparin conjugated to Sepharose. Our results demonstrate that a protein unrelated to laminin or its associated macromolecules and which copurifies with the type II cAMP-dPK of striated muscle stimulates neurite outgrowth from neurons of the central and peripheral nervous systems.

摘要

脊髓运动神经元的发育与存活依赖于肌肉衍生的营养因子。一些间接证据使我们推测,环磷酸腺苷(cAMP)依赖性蛋白激酶(cAMP-dPK)II型的调节亚基可能参与脊髓神经元的神经突生长。在本研究中,我们测试了一种市售的cAMP-dPK制剂的促神经突生长活性。当将来自骨骼肌和心肌的市售cAMP-dPK II型酶制剂与聚赖氨酸包被的基质结合时,可诱导培养的胚胎鸡神经元显著长出神经突;而来自骨骼肌的I型cAMP-dPK则无此作用。I型和II型cAMP-dPK对培养的脊髓神经元的存活均无显著影响。II型cAMP-dPK还能刺激培养的鸡脑半球神经元、背根神经节神经元、睫状神经节神经元以及大鼠交感神经节神经元长出神经突。促神经突生长活性似乎存在于该制剂的一种污染物中,因为纯化的II型cAMP-dPK调节亚基和催化亚基本身对培养神经元的神经突生长均无影响,且促神经突生长活性与[3H]cAMP结合或cAMP依赖性激酶活性无关。然后,通过在Sephadex G-200上进行凝胶过滤,随后在DE-52纤维素上进行离子交换色谱,从市售的II型cAMP-dPK中部分纯化了促神经突生长蛋白。活性蛋白峰的十二烷基硫酸钠凝胶电泳显示出一条主要蛋白带(分子量50 kDa)和几条次要蛋白带(例如分子量200 kDa、52 kDa、45 kDa)。此外,免疫印迹分析和免疫沉淀表明,部分纯化的促神经突生长蛋白与层粘连蛋白、硫酸乙酰肝素蛋白聚糖、神经生长因子、神经细胞黏附分子和纤连蛋白不同。此外,用肝素酶处理后促神经突生长活性并未降低,且它也不与偶联到琼脂糖上的肝素结合。我们的结果表明,一种与层粘连蛋白或其相关大分子无关且与横纹肌II型cAMP-dPK共纯化的蛋白可刺激中枢和外周神经系统神经元的神经突生长。

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