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经滤器诱导的后肾间充质中细胞糖缀合物的表达

Expression of cellular glycoconjugates in transfilter-induced metanephric mesenchyme.

作者信息

Laitinen L, Virtanen I, Saxén L, Lehtonen E

机构信息

Department of Pathology, University of Helsinki, Finland.

出版信息

Anat Rec. 1988 Feb;220(2):190-7. doi: 10.1002/ar.1092200210.

Abstract

Expression of glycoconjugates during transfilter-induced differentiation of metanephric mesenchyme was studied by using fluorochrome- and peroxidase-coupled lectins. All cells in the uninduced metanephric mesenchyme expressed mannose, beta-D-galactose (beta-Gal), N-acetylglucosamine (GlucNAc), and terminal sialic acids. Additionally, solitary cells showed terminal alpha-D-galactose alpha-D-galactose (alpha-Gal) typical of mouse endothelial cells. During culture, undifferentiated mesenchymal cells seemed to disappear from induced explants, and many of the stromal cells between the evolving tubules presented terminal alpha-Gal residues. Similar positivity could be revealed in monolayer cultures of induced mesenchymes. A number of tubules in induced explants displayed alpha-L-fucosyl (Fuc) residues, characteristic of mature proximal tubules. Some terminal Ga1NAc residues, recognized only by Dolichos biflorus agglutinin, emerged in a few tubular cells after prolonged culture. The early tubules and glomerular bodies displayed a basement membrane presenting both terminal Ga1-(beta 1-3)-Ga1NAc and Ga1NAc residues. These positivities disappeared later from many tubular structures and glomerular bodies but persisted in tubules expressing proximal tubular differentiation. The glomerular bodies displayed only one cell type, reminiscent of maturing podocytes, presenting terminal Ga1-(beta 1-3)-Ga1NAc and Ga1NAc residues. Later these saccharide residues became covered by sialylation, as they could then be revealed only after treatment with neuraminidase. The results indicate that the segment-specific expression of saccharide residues during differentiation of nephron in vitro resembles the sequence seen in vivo. This study also suggests that the basement membranes surrounding the nephron show a stepwise, segment-specific maturation. Despite the presence of endothelial cells in the metanephric explants, only avascular glomeruli evolved in this differentiation model.

摘要

利用荧光染料和过氧化物酶偶联凝集素,研究了转滤诱导后肾间充质分化过程中糖缀合物的表达。未诱导的后肾间充质中的所有细胞均表达甘露糖、β-D-半乳糖(β-Gal)、N-乙酰葡糖胺(GlucNAc)和末端唾液酸。此外,单个细胞显示出典型的小鼠内皮细胞的末端α-D-半乳糖α-D-半乳糖(α-Gal)。在培养过程中,未分化的间充质细胞似乎从诱导的外植体中消失,并且在发育中的肾小管之间的许多基质细胞呈现末端α-Gal残基。在诱导间充质的单层培养物中也可显示出类似的阳性反应。诱导外植体中的许多肾小管显示出α-L-岩藻糖基(Fuc)残基,这是成熟近端肾小管的特征。仅由双花扁豆凝集素识别的一些末端GalNAc残基在长时间培养后出现在少数肾小管细胞中。早期的肾小管和肾小球体显示出同时呈现末端Gal-(β1-3)-GalNAc和GalNAc残基的基底膜。这些阳性反应后来在许多肾小管结构和肾小球体中消失,但在表达近端肾小管分化的肾小管中持续存在。肾小球体仅显示一种细胞类型,让人联想到成熟的足细胞,呈现末端Gal-(β1-3)-GalNAc和GalNAc残基。后来这些糖残基被唾液酸化覆盖,因为只有在用神经氨酸酶处理后才能显示出来。结果表明,体外肾单位分化过程中糖残基的节段特异性表达类似于体内所见的序列。这项研究还表明,围绕肾单位的基底膜显示出逐步的、节段特异性的成熟。尽管后肾外植体中存在内皮细胞,但在这种分化模型中仅形成了无血管的肾小球。

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