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小鼠回肠派尔集合淋巴结中微皱褶细胞的结构、分布及起源

Structure, distribution, and origin of M cells in Peyer's patches of mouse ileum.

作者信息

Bye W A, Allan C H, Trier J S

出版信息

Gastroenterology. 1984 May;86(5 Pt 1):789-801.

PMID:6706062
Abstract

The derivation of membranous epithelial (M) cells, which are specialized antigen sampling cells overlying the lymphoid follicles of Peyer's patches, is unknown; it has been suggested recently, however, that M cells differentiate from absorptive cells on the follicular epithelium. To examine whether M cells, like other intestinal epithelial cells, derive directly from undifferentiated crypt cells, we studied the structure, selected functional features, proliferation, and distribution of Peyer's patch M cells in the ileum of adult mice. We observed a spectrum of M-cell structure ranging from mature to immature-appearing M cells. Most immature-appearing M cells lacked the central cytoplasmic hollow found in those mature M cells that contained lymphoid cells. The microvilli of immature-appearing M cells were more numerous and regular appearing than those of mature M cells, but they were sparser and shorter, and some were wider than those of absorptive cells. Many immature-appearing M cells contained more free ribosomes than did mature M cells. Both mature and immature-appearing M cells were observed on all regions of follicular domes, including the base near the mouths of surrounding crypts. Type 1 reovirions adhered with considerable selectivity to the apical membrane of mature and immature-appearing M cells but were observed in endocytic vesicles only in mature M cells. Neither mature nor immature-appearing M cells showed evidence of lipid absorption, in contrast to adjacent absorptive cells. Both mature and immature-appearing M cells internalized more bound cationized ferritin than did absorptive cells. Only mature M cells transported cationized ferritin to the intercellular spaces. Nuclei of a few immature-appearing M cells were labeled 24 h after injection of [3H]thymidine in concert with the appearance of labeled absorptive cell nuclei. These observations strongly suggest that many, if not all, M cells derive directly from undifferentiated crypt cells.

摘要

膜性上皮(M)细胞是位于派尔集合淋巴结淋巴滤泡上方的特殊抗原采样细胞,其来源尚不清楚;然而,最近有人提出M细胞是由滤泡上皮的吸收细胞分化而来。为了研究M细胞是否像其他肠道上皮细胞一样直接来源于未分化的隐窝细胞,我们研究了成年小鼠回肠中派尔集合淋巴结M细胞的结构、选定的功能特征、增殖和分布。我们观察到一系列M细胞结构,从成熟的到看起来不成熟的M细胞。大多数看起来不成熟的M细胞缺乏在含有淋巴细胞的成熟M细胞中发现的中央细胞质空洞。看起来不成熟的M细胞的微绒毛比成熟M细胞的更多且更规则,但它们比吸收细胞的微绒毛更稀疏、更短,有些还更宽。许多看起来不成熟的M细胞比成熟M细胞含有更多的游离核糖体。在滤泡圆顶的所有区域都观察到了成熟和看起来不成熟的M细胞,包括周围隐窝口附近的基部。1型呼肠孤病毒对成熟和看起来不成熟的M细胞的顶端膜有相当的选择性粘附,但仅在成熟M细胞的内吞小泡中观察到。与相邻的吸收细胞相比,成熟和看起来不成熟的M细胞均未显示脂质吸收的证据。成熟和看起来不成熟的M细胞内化的结合阳离子铁蛋白均比吸收细胞多。只有成熟M细胞将阳离子铁蛋白转运到细胞间隙。注射[3H]胸苷24小时后,一些看起来不成熟的M细胞的细胞核被标记,同时出现标记的吸收细胞核。这些观察结果强烈表明,许多(如果不是全部)M细胞直接来源于未分化的隐窝细胞。

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