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Neurogenic origin of human prostate endocrine cells.

机译:人前列腺内分泌细胞的神经源性起源。

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OBJECTIVES: To determine the histogenetic origin of prostate neuroendocrine cells in human embryos. METHODS: Prostatic tissue in human fetuses, ranging in gestational age from early week 10 to term, and infantile and pubertal glands were studied immunohistochemically. The distribution of neuroendocrine cells within the developing gland was semiquantitatively determined. Antibodies against the neuroendocrine markers chromogranin A (CgA) and protein gene product 9.5 (PGP), along with markers of prostatic secretion (prostate-specific antigen [PSA], prostatic acid phosphatase [PAP]), were used. They were applied either individually or in double-labeling experiments, as well as in experiments combining CgA immunohistochemical analysis with in situ hybridization or in situ end-labeling. RESULTS: In embryos of less than 65-mm crown-rump length (CRL) (ie, younger than 12 weeks of gestation), the epithelium of the urogenital sinus was free of endocrine cells. On either side of the future prostatic mesenchyme, paraganglia containing CgA-immunoreactive cells are present, which start to penetrate the urogenital mesenchyme. In the late 10th week, these CgA-immunoreactive cells are found dispersed in the urogenital mesenchyme. In embryos of 65-mm CRL, when prostatic anlagen start to sprout from the urogenital epithelium, very few (but typically shaped) neuroendocrine cells appear in the urogenital sinus epithelium. Later, after the 12th week, when solid prostatic ducts have started forming, CgA-immunoreactive neuroendocrine cells are also present in these buds. The number of neuroendocrine cells in the urethral epithelium is considerably increased, and with the continuous sprouting and lumen formation of prostatic anlagen, neuroendocrine cells are transported into the future gland. Neuroendocrine cells observed in stroma of prenatal and postnatal prostates may also contribute to the neuroendocrine cell population of the gland. CONCLUSIONS: Our results provide the first evidence that human prostate neuroendocrine cells represent a cell lineage of their own, being of neurogenic origin and therefore distinct from the urogenital sinus-derived prostate secretory and basal cells.
机译:目的:确定人类胚胎中前列腺神经内分泌细胞的组织遗传学起源。方法:采用免疫组织化学方法对人胎儿的前列腺组织进行了研究,从胎龄早十周到足月,以及婴儿和青春期的腺体。半定量确定发育中腺内神经内分泌细胞的分布。使用了针对神经内分泌标记物嗜铬粒蛋白A(CgA)和蛋白质基因产物9.5(PGP)的抗体,以及前列腺分泌的标记物(前列腺特异性抗原[PSA],前列腺酸性磷酸酶[PAP])。它们可以单独使用,也可以用于双标记实验,也可以用于结合CgA免疫组织化学分析与原位杂交或原位末端标记的实验。结果:在小于65毫米冠臀长(CRL)的胚胎(即小于12周妊娠的胚胎)中,泌尿生殖窦的上皮没有内分泌细胞。在未来的前列腺间充质的任何一侧,都存在含有CgA免疫反应性细胞的旁神经节,该细胞开始渗透到泌尿生殖道间质。在第10周后期,发现这些CgA免疫反应性细胞分散在泌尿生殖道间质中。在65毫米CRL的胚胎中,当前列腺尿囊素开始从泌尿生殖道上皮发芽时,泌尿生殖窦上皮中几乎没有(但通常是成形的)神经内分泌细胞出现。随后,在第12周后,当开始形成固体前列腺导管时,这些芽中也存在CgA免疫反应性神经内分泌细胞。尿道上皮中神经内分泌细胞的数量大大增加,并且随着前列腺胶原蛋白的不断发芽和管腔形成,神经内分泌细胞被转运到未来的腺体中。在产前和产后前列腺的基质中观察到的神经内分泌细胞也可能有助于腺体的神经内分泌细胞群。结论:我们的结果提供了第一个证据,证明人类前列腺神经内分泌细胞代表了自己的细胞谱系,具有神经源性,因此不同于泌尿生殖窦来源的前列腺分泌和基底细胞。

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