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脂肪组织细胞外基质:在分化过程中由脂肪细胞重新构建。

Adipose tissue extracellular matrix: newly organized by adipocytes during differentiation.

作者信息

Nakajima I, Yamaguchi T, Ozutsumi K, Aso H

机构信息

Department of Animal Physiology, National Institute of Animal Industry, Ibaraki, Japan.

出版信息

Differentiation. 1998 Aug;63(4):193-200. doi: 10.1111/j.1432-0436.1998.00193.x.

Abstract

The distribution of eight types of extracellular matrix (ECM) proteins (type I-VI) collagen, laminin and fibronectin) in the skeletal muscle of Japanese Black cattle was determined by indirect immunofluorescence using specific antibodies against each protein. ECM proteins were well organized in the intramuscular connective tissue: type I, II, III collagen and fibronectin were localized primarily in the perimysium, type V and VI collagen in both the perimysium and endomysium, and type IV collagen and laminin were virtually confined to the endomysium. In the loose connective tissue holding the adipocytes together to form a tissue mass between the muscular bundles, seven of the ECM proteins not type II collagen were relatively abundant in a disordered arrangement. Further analysis by in vitro immunocytochemical staining also demonstrated that a stromal-vascular preadipocyte cell line (BIP cell), derived from Japanese Black cattle, synthesized various ECMs in much the same way as fibroblasts. Exponentially growing BIP cells with a fibroblastic phenotype were found to produce type II, V, and VI collagens, in addition to the other previously identified connective tissue glycoproteins of mouse 3T3 preadipocytes. When confluent preadipocyte cultures were stimulated with adipogenic medium, a fibrillar network of ECM was observed to bridge the intercellular space and connect adjacent cell surfaces. During adipocyte differentiation, type III collagen and laminin were arranged in a non-fibrous structure, and type-II collagen was only barely detected. These results are supported by the staining of the adipose tissue, where all ECM proteins studied except type II collagen were stained intensely. These data indicate that in vivo under conditions permissive for adipose conversion, the production and organization of ECM, accompanied by hyperplasia and hypertrophy of precursor cells, gives rise to adipose tissue in skeletal muscle with its own ECM products. These data further suggest that each ECM protein might have some role for the adipocytes in forming tissue.

摘要

利用针对每种蛋白质的特异性抗体,通过间接免疫荧光法测定了日本黑牛骨骼肌中八种细胞外基质(ECM)蛋白(I - VI型胶原蛋白、层粘连蛋白和纤连蛋白)的分布。ECM蛋白在肌内结缔组织中排列有序:I型、II型、III型胶原蛋白和纤连蛋白主要定位于肌束膜,V型和VI型胶原蛋白在肌束膜和肌内膜中均有分布,IV型胶原蛋白和层粘连蛋白几乎局限于肌内膜。在将脂肪细胞聚集在一起形成肌束间组织块的疏松结缔组织中,除II型胶原蛋白外的七种ECM蛋白以无序排列的形式相对丰富。体外免疫细胞化学染色进一步分析表明,源自日本黑牛的基质血管前脂肪细胞系(BIP细胞)合成各种ECM的方式与成纤维细胞大致相同。发现具有成纤维细胞表型且呈指数生长的BIP细胞除了产生小鼠3T3前脂肪细胞先前鉴定的其他结缔组织糖蛋白外,还产生II型、V型和VI型胶原蛋白。当用脂肪生成培养基刺激汇合的前脂肪细胞培养物时,观察到ECM的纤维状网络跨越细胞间空间并连接相邻细胞表面。在脂肪细胞分化过程中,III型胶原蛋白和层粘连蛋白呈非纤维结构排列,而II型胶原蛋白仅勉强检测到。这些结果得到了脂肪组织染色的支持,在脂肪组织中,除II型胶原蛋白外,所有研究的ECM蛋白均被强烈染色。这些数据表明,在允许脂肪转化的体内条件下,ECM的产生和组织伴随着前体细胞的增生和肥大,导致骨骼肌中形成具有自身ECM产物的脂肪组织。这些数据进一步表明,每种ECM蛋白可能在脂肪细胞形成组织中发挥某种作用。

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