首页> 美国卫生研究院文献>Reproductive Biology and Endocrinology : RBE >Multiple luteinizing hormone receptor (LHR) protein variants interspecies reactivity of anti-LHR mAb clone 3B5 subcellular localization of LHR in human placenta pelvic floor and brain and possible role for LHR in the development of abnormal pregnancy pelvic floor disorders and Alzheimers disease
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Multiple luteinizing hormone receptor (LHR) protein variants interspecies reactivity of anti-LHR mAb clone 3B5 subcellular localization of LHR in human placenta pelvic floor and brain and possible role for LHR in the development of abnormal pregnancy pelvic floor disorders and Alzheimers disease

机译:多种黄体生成激素受体(LHR)蛋白变体抗LHR mAb克隆3B5的种间反应性LHR在人胎盘骨盆底和脑中的亚细胞定位以及LHR在异常妊娠骨盆底疾病和阿尔茨海默氏病发展中的可能作用疾病

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摘要

Distinct luteinizing hormone receptor (LHR) protein variants exist due to the posttranslational modifications. Besides ovaries, LHR immunoreactivity (LHRI) was also found in other tissues, such as the brain, fallopian tube, endometrium, trophoblast and resident tissue macrophages. The 3B5 mouse monoclonal antibody was raised against purified rat LHR. In rat, porcine and human ovaries, the 3B5 identified six distinct LHR bands migrating at ~92, 80, 68, 59, 52 and 48 kDa. Characteristic LHRI was detected in rat, human and porcine corpora lutea. During cellular differentiation, subcellular LHR distribution changed from none to granular cytoplasmic, perinuclear, surface, nuclear and no staining. There were also differences in vascular LHR expression – lack of LHRI in ovarian vessels and strong staining of vessels in other tissues investigated. In normal human term placentae, villous LHRI was associated with blood sinusoids and cytotrophoblast cells, and rarely detected in trophoblastic syncytium. In all abnormal placentae, the LHRI of sinusoids was absent, and syncytium showed either enhanced (immature placental phenotypes) or no LHRI (aged placental phenotype). LHRI in human brain was identified in microglial cells (CD68+ resident macrophages). Protein extracts from human vaginal wall and levator ani muscle and fascia showed strong ~92 and 68 kDa species, and LHRI was detected in smooth muscle cells, fibroblasts, resident macrophages and nuclei of skeletal muscle fibers. Our observations indicate that, in contrast to the theory on the role of vascular hormone receptors in preferential pick up of circulating hormones, there is no need to enhance selective pick up rather only prevent LH/CG transport to inappropriate sites. Abnormal placental LHR expression may play a role in the development of abnormal pregnancy. Expression of LHR in the pelvic floor compartments suggests that high LH levels in postmenopausal women may contribute to the pelvic floor relaxation and increased incidence of pelvic floor disorders. Since chorionic gonadotropin increases secretion of a variety of cytokines by monocytes, and induces their inflammatory reaction and phagocytic activity, high LH levels in aging individuals may also activate microglia (mononuclear phagocyte system in the central nervous system) and contribute to the development of Alzheimer's disease and other inflammation-mediated neurodegenerative diseases.
机译:由于翻译后修饰,存在不同的黄体生成激素受体(LHR)蛋白变体。除卵巢外,在其他组织中也发现了LHR免疫反应性(LHRI),例如大脑,输卵管,子宫内膜,滋养细胞和常驻组织巨噬细胞。产生了针对纯化的大鼠LHR的3B5小鼠单克隆抗体。在大鼠,猪和人的卵巢中,3B5鉴定出以〜92、80、68、59、52和48 kDa迁移的六个不同的LHR条带。在大鼠,人和猪黄体中检测到特征性LHRI。在细胞分化过程中,亚细胞LHR分布从无改变为颗粒状胞质,核周,表面,核和无染色。血管中LHR的表达也有差异-卵巢血管中缺乏LHRI,而其他组织中的血管则染色强烈。在正常人足月胎盘中,绒毛状LHRI与血窦和细胞滋养细胞有关,很少在滋养细胞合胞体中检测到。在所有异常胎盘中,不存在正弦曲线的LHRI,合胞体显示增强(胎盘表型未成熟)或无LHRI(胎盘表型老化)。在小胶质细胞(CD68 +常驻巨噬细胞)中鉴定出人脑中的LHRI。来自人阴道壁和肛提肌及筋膜的蛋白质提取物显示出约92和68 kDa的强种,在平滑肌细胞,成纤维细胞,驻留巨噬细胞和骨骼肌纤维核中检测到LHRI。我们的观察表明,与关于血管激素受体在优先摄取循环激素中的作用的理论相反,没有必要增强选择性摄取,而仅是防止LH / CG转运到不合适的部位。胎盘LHR表达异常可能在异常妊娠的发展中起作用。 LHR在骨盆底隔室中的表达表明,绝经后妇女中的高LH水平可能会导致骨盆底松弛和增加骨盆底疾病的发生率。由于绒毛膜促性腺激素会增加单核细胞分泌多种细胞因子,并诱导其炎症反应和吞噬活性,因此衰老个体的高LH水平也可能激活小胶质细胞(中枢神经系统中的单核吞噬细胞系统),并有助于阿尔茨海默氏病的发展和其他炎症介导的神经退行性疾病。

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