Kordeli E, Bennett V
Howard Hughes Medical Institute, Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710.
J Cell Biol. 1991 Sep;114(6):1243-59. doi: 10.1083/jcb.114.6.1243.
Isoforms of ankyrin (ankyrinsR) immunologically related to erythrocyte ankyrin (ankyrinRo) are associated with distinct neuronal plasma membrane domains of functional importance, such as cell bodies and dendrites, axonal hillock and initial segments, and nodes of Ranvier. AnkyrinRo is expressed in brain, and accounts for at least one of the ankyrinR isoforms. Another ankyrin isoform of brain, ankyrinB, is encoded by a distinct gene and is immunologically distinct from ankyrinsR. Mutant mice with normoblastosis (nb/nb) constitute the first described genetic model of ankyrin deficiency: they display a severe hemolytic anemia due to a significantly reduced expression of the ankyrinRo gene in reticulocytes as well as brain (Peters L. L., C. S. Birkenmeier, R. T. Bronson, R. A. White, S. E. Lux, E. Otto, V. Bennett, A. Higgins, and J. E. Barker. 1991. J. Cell Biol. 114:1233-1241). In the present report, we distinguish between ankyrinRo and other ankyrinR isoforms using immunoblot analysis and immunofluorescence localization of ankyrinsR throughout the nervous system (forebrain, cerebellum, brain stem, spinal cord, and sciatic nerve) of nb/nb and normal mice. This is the first immunocytochemical characterization of the neurological component of the nb mutation and shows the following. (a) The isoform of ankyrin at the nodes of Ranvier and initial axonal segments is present in the nb/nb mice and does not cross-react with an ankyrinRo-specific antibody; this isoform, therefore, is distinct from both ankyrin isoforms identified in brain, ankyrinRo and ankyrinB, and is probably the product of a distinct gene and a unique component of the specialized membrane skeleton associated with nodes of Ranvier. (b) AnkyrinRo missing from nb/nb mice is selectively associated with neuronal cell bodies and dendrites, excluded from myelinated axons, and displays a selective pattern of expression in the nervous system whereby expression is almost ubiquitous in neurons of the cerebellum (Purkinje and granule cells) and spinal cord, and restricted to a very minor subset of neurons in hippocampus and neocortex of forebrain.
与红细胞锚蛋白(ankyrinRo)存在免疫相关性的锚蛋白异构体(ankyrinsR),与具有功能重要性的不同神经元质膜结构域相关联,如细胞体和树突、轴突丘和起始节段,以及郎飞结。AnkyrinRo在脑中表达,并且是ankyrinR异构体中的至少一种。脑中的另一种锚蛋白异构体ankyrinB,由一个不同的基因编码,并且在免疫上与ankyrinsR不同。患有幼红细胞增多症(nb/nb)的突变小鼠构成了首个被描述的锚蛋白缺乏的遗传模型:由于网织红细胞以及脑中ankyrinRo基因的表达显著降低,它们表现出严重的溶血性贫血(彼得斯L.L.、C.S.比尔肯迈尔、R.T.布朗森、R.A.怀特、S.E.勒克斯、E.奥托、V.贝内特、A.希金斯和J.E.巴克。1991年。《细胞生物学杂志》114:1233 - 1241)。在本报告中,我们通过免疫印迹分析以及对nb/nb和正常小鼠整个神经系统(前脑、小脑、脑干、脊髓和坐骨神经)中ankyrinsR的免疫荧光定位,区分了ankyrinRo和其他ankyrinR异构体。这是对nb突变的神经学成分的首次免疫细胞化学表征,结果如下。(a)郎飞结和轴突起始节段处的锚蛋白异构体存在于nb/nb小鼠中,并且不与ankyrinRo特异性抗体发生交叉反应;因此,这种异构体与在脑中鉴定出的两种锚蛋白异构体ankyrinRo和ankyrinB都不同,并且可能是一个不同基因的产物,是与郎飞结相关的特殊膜骨架的独特成分。(b)nb/nb小鼠中缺失的ankyrinRo与神经元细胞体和树突选择性相关,被排除在有髓轴突之外,并且在神经系统中呈现出一种选择性表达模式,即其表达在小脑(浦肯野细胞和颗粒细胞)和脊髓的神经元中几乎普遍存在,而在前脑的海马体和新皮质中则局限于非常小的一部分神经元。