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首页> 外文期刊>Anatomy and embryology >Postnatal differentiation of Merkel cells in the rat palatine mucosa, with special reference to the timing of peripheral nerve development and the potency of cell mitosis.
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Postnatal differentiation of Merkel cells in the rat palatine mucosa, with special reference to the timing of peripheral nerve development and the potency of cell mitosis.

机译:鼠kel粘膜中默克尔细胞的产后分化,特别涉及周围神经发育的时机和细胞有丝分裂的潜能。

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摘要

The origin and mechanism of the differentiation and proliferation of Merkel cells are enigmatic. A preliminary study in our laboratory showed that Merkel cells in the rat palatine mucosa emerge after birth. This is in contrast to the case of similar cells in the skin that differentiate during the embryonic period prior to the establishment of peripheral nerve innervation. We studied immunohistochemically the developmental timings of Merkel cells and peripheral nerves in the rat palatine mucosa using antibodies to cytokeratins 18 and 20, PGP 9.5, and CGRP using developing palates of prenatal and postnatal rats. We also studied the potency of mitosis in Merkel cells by immunohistochemistry using antibodies for a cell proliferation marker Ki67 and cyclin D-kinase inhibitors p16, p21 and p27. It was shown that Merkel cells in the rat palatine mucosa differentiate postnatally, after the development of peripheral nerve fiber terminals was almost established. The emergence and increase in number of Merkel cells progressed in an anterior-to-posterior wave. Newly appearing Merkel cells were usually negative for anti-cytokeratin 20 antibody but gained affinity for the antibody with progress of maturation. All Merkel cells in the palatine mucosa were negative for anti-Ki67 antibody but positive for anti-p27 antibody. These results indicate that Merkel cells in the rat palatine mucosa are not responsible for the development of peripheral nerve fiber terminals and that these cells differentiate in situ from intraepithelial stem cells.
机译:默克尔细胞分化和增殖的起源和机制是谜。我们实验室的初步研究表明,鼠p黏膜中的默克尔细胞在出生后就会出现。这与皮肤中类似细胞在周围神经支配建立之前的胚胎时期分化的情况相反。我们使用免疫球化学方法使用产前和产后大鼠的裂对细胞角蛋白18和20,PGP 9.5和CGRP的抗体,对大鼠the粘膜中默克尔细胞和周围神经的发育时机进行了研究。我们还使用细胞增殖标记Ki67和细胞周期蛋白D激酶抑制剂p16,p21和p27的抗体,通过免疫组织化学研究了默克尔细胞中有丝分裂的效力。结果表明,在几乎确定了周围神经纤维末端的发育之后,大鼠p黏膜中的默克尔细胞会在出生后分化。默克尔细胞的出现和增加以前后波的形式进行。新出现的默克尔细胞通常对抗细胞角蛋白20抗体呈阴性,但随着成熟的进展对抗体具有亲和力。 ala粘膜中的所有默克尔细胞均抗Ki67抗体阴性,但抗p27抗体阳性。这些结果表明,大鼠p粘膜中的默克尔细胞不负责周围神经纤维末端的发育,并且这些细胞与上皮内干细胞原位分化。

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