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神经营养因子-3基因敲除小鼠中默克尔细胞的凋亡

Apoptosis of Merkel cells in neurotrophin-3 null mice.

作者信息

Halata Zdenek, Kucera Jan, Kucera Tomas, Grim Milos

机构信息

Institute of Functional Morphology, University of Hamburg, Martinstrasse 52, 22045 Hamburg, Germany.

出版信息

Anat Embryol (Berl). 2005 Apr;209(4):335-40. doi: 10.1007/s00429-005-0455-0. Epub 2005 Mar 2.

Abstract

Postnatal mice lacking neurotrophin-3 (NT3) are deficient in Merkel cells of touch domes and whisker follicles. We examined the mechanism of Merkel cell loss by immunocytochemistry and electron microscopy. Merkel cell of whisker follicles of NT3 null newborns exhibited decreased immunoreactivity for cytokeratin 8 and contained apoptotic bodies that were positive for cleaved caspase-3, a marker of active apoptosis. By electron microscopy, the Merkel cells displayed aggregation of chromatin along the nuclear membrane, with the marginated chromatin forming caps at the periphery of the nucleus. Ribosomes aggregated in the cytoplasm, while dense core granules characteristic of Merkel cells were still discernible. Finally, the Merkel cells and their nuclei fragmented into apoptotic bodies. None of the apoptotic Merkel cells were contacted by nerve fibers, and their desmosomal contacts with surrounding keratinocytes disappeared. After postnatal day 6 apoptotic Merkel cells were no longer observed, and the number of surviving Merkel cells was severely reduced. They were flat and contained few osmiophilic granules. We conclude that perinatal apoptosis is responsible for the loss of Merkel cells lacking innervation in NT3 null mice.

摘要

缺乏神经营养因子-3(NT3)的出生后小鼠,其触盘和触须毛囊中的默克尔细胞存在缺陷。我们通过免疫细胞化学和电子显微镜检查了默克尔细胞丢失的机制。NT3基因敲除新生小鼠触须毛囊中的默克尔细胞,细胞角蛋白8的免疫反应性降低,并含有凋亡小体,这些凋亡小体对活化凋亡的标志物——裂解的半胱天冬酶-3呈阳性。通过电子显微镜观察,默克尔细胞的染色质沿核膜聚集,边缘化的染色质在核周边形成帽状。核糖体在细胞质中聚集,而默克尔细胞特有的致密核心颗粒仍可辨认。最后,默克尔细胞及其细胞核破碎成凋亡小体。没有神经纤维与凋亡的默克尔细胞接触,并且它们与周围角质形成细胞的桥粒连接消失。出生后第6天之后,不再观察到凋亡的默克尔细胞,存活的默克尔细胞数量严重减少。它们扁平,含有很少的嗜锇颗粒。我们得出结论,围产期凋亡是NT3基因敲除小鼠中缺乏神经支配的默克尔细胞丢失的原因。

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