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神经元微管相关蛋白2D是一种在大鼠卵巢颗粒细胞中表达的双a激酶锚定蛋白。

Neuronal microtubule-associated protein 2D is a dual a-kinase anchoring protein expressed in rat ovarian granulosa cells.

作者信息

Salvador Lisa M, Flynn Maxfield P, Avila Jesús, Reierstad Scott, Maizels Evelyn T, Alam Hena, Park Youngkyu, Scott John D, Carr Daniel W, Hunzicker-Dunn Mary

机构信息

Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA.

出版信息

J Biol Chem. 2004 Jun 25;279(26):27621-32. doi: 10.1074/jbc.M402980200. Epub 2004 Mar 31.

Abstract

A-kinase anchoring proteins (AKAPs) function to target protein kinase A (PKA) to specific locations within the cell. AKAPs are functionally identified by their ability to bind the type II regulatory subunits (RII) of PKA in an in vitro overlay assay. We previously showed that follicle-stimulating hormone (FSH) induces the expression of an 80-kDa AKAP (AKAP 80) in ovarian granulosa cells as they mature from a preantral to a preovulatory phenotype. In this report, we identify AKAP 80 as microtubule-associated protein 2D (MAP2D), a low molecular weight splice variant of the neuronal MAP2 protein. MAP2D is induced in granulosa cells by dexamethasone and by FSH in a time-dependent manner that mimics that of AKAP 80, and immunoprecipitation of MAP2D depletes extracts of AKAP 80. MAP2D is the only MAP2 protein present in ovaries and is localized to granulosa cells of preovulatory follicles and to luteal cells. MAP2D is concentrated at the Golgi apparatus along with RI and RII and, based on coimmunoprecipitation results, appears to bind both RI and RII in granulosa cells. Reduced expression of MAP2D resulting from treatment of granulosa cells with antisense oligonucleotides to MAP2 inhibited the phosphorylation of cAMP-response element-binding protein. These results suggest that this classic neuronal RII AKAP is a dual RI/RII AKAP that performs unique functions in ovarian granulosa cells that contribute to the preovulatory phenotype.

摘要

A激酶锚定蛋白(AKAPs)的功能是将蛋白激酶A(PKA)靶向细胞内的特定位置。在体外覆盖分析中,AKAPs通过其结合PKA II型调节亚基(RII)的能力在功能上得以鉴定。我们之前发现,随着卵巢颗粒细胞从前窦状卵泡成熟为排卵前卵泡表型,促卵泡激素(FSH)会诱导一种80 kDa的AKAP(AKAP 80)表达。在本报告中,我们确定AKAP 80为微管相关蛋白2D(MAP2D),它是神经元MAP2蛋白的一种低分子量剪接变体。地塞米松和FSH能以时间依赖性方式诱导颗粒细胞中MAP2D的表达,这种方式与AKAP 80相似,且对MAP2D进行免疫沉淀会耗尽AKAP 80提取物。MAP2D是卵巢中唯一存在的MAP2蛋白,定位于排卵前卵泡的颗粒细胞和黄体细胞。MAP2D与RI和RII一起集中在高尔基体,基于共免疫沉淀结果,它似乎在颗粒细胞中同时结合RI和RII。用针对MAP2的反义寡核苷酸处理颗粒细胞导致MAP2D表达降低,这抑制了环磷酸腺苷反应元件结合蛋白的磷酸化。这些结果表明,这种经典的神经元RII AKAP是一种双重RI/RII AKAP,在卵巢颗粒细胞中发挥独特功能,有助于形成排卵前卵泡表型。

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