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通过软骨模型形成骨骼:“边缘”软骨细胞。

Bone formation via cartilage models: the "borderline" chondrocyte.

作者信息

Bianco P, Cancedda F D, Riminucci M, Cancedda R

机构信息

Department of Experimental Medicine, University of Aquila, Italy.

出版信息

Matrix Biol. 1998 Jul;17(3):185-92. doi: 10.1016/s0945-053x(98)90057-9.

Abstract

Increasing evidence substantiates the view that death is not necessarily the only fate of hypertrophic chondrocytes and that, when exposed to the right microenvironment, these cells can further differentiate to osteoblast-like cells and contribute to initial bone formation. In vitro, when replated as adherent cells in the presence of ascorbic acid, hypertrophic chondrocytes resume cell proliferation, switch from the synthesis of the cartilage-characteristic type II and X collagens to the synthesis of type I collagen, and organize a mineralizing bone matrix. In vivo, expression of bone specific markers by growth plate chondrocytes occurs initially in early hypertrophic cells located at the mid-diaphysis and directly facing the osteogenic perichondrium. In bones formed via cartilage models, the first mineralized bone matrix (the earliest bony collar preceding vascular invasion and the onset of endochondral bone formation) is deposited at the outer aspect of the mid-diaphysis between rows of early hypertrophic chondrocytes and osteoblasts, which are arranged in a peculiar "vis à vis" fashion. The "vis à vis" organization of perichondrial osteogenic cells and peripheral early hypertrophic chondrocytes suggests that the latter cells are exposed -- compared to their cognate, the central hypertrophic chondrocytes -- to a specific microenvironment composed of unique matrix-originating signals and cellular cross-talks. A major role in the differentiation control of, and interaction between, hypertrophic chondrocytes and osteogenic perichondrial cells is certainly played by the Indian Hedgehog/PTHrP signalling system. We propose that all early hypertrophic chondrocytes have the inherent potential to differentiate to osteoblast-like cells and to contribute to initial bone formation, but that only chondrocytes positioned at the "borderland" between cartilage and (non-cartilage) osteogenic tissues undergo further differentiation to bone producing cells. We call these hypertrophic chondrocytes "borderline chondrocytes" to emphasize both their specific location and their dual differentiation potential. Hypertrophic chondrocytes located in different cartilage areas are exposed to an inappropriate matrix and endocrine/paracrine environment, cannot differentiate to osteoblast-like cells and therefore undergo apoptosis.

摘要

越来越多的证据支持以下观点

死亡不一定是肥大软骨细胞的唯一命运,并且当暴露于合适的微环境时,这些细胞可以进一步分化为成骨样细胞并有助于初始骨形成。在体外,当在抗坏血酸存在下作为贴壁细胞重新接种时,肥大软骨细胞恢复细胞增殖,从合成软骨特征性的II型和X型胶原转变为合成I型胶原,并组织矿化骨基质。在体内,生长板软骨细胞中骨特异性标志物的表达最初发生在位于骨干中部并直接面对成骨软骨膜的早期肥大细胞中。在通过软骨模型形成的骨骼中,第一个矿化骨基质(在血管侵入和软骨内骨形成开始之前最早的骨环)沉积在骨干中部的外侧,位于排成行的早期肥大软骨细胞和成骨细胞之间,它们以一种特殊的“面对面”方式排列。软骨膜成骨细胞和外周早期肥大软骨细胞的“面对面”组织表明,与它们的同源细胞——中央肥大软骨细胞相比,后者细胞暴露于由独特的基质起源信号和细胞间相互作用组成的特定微环境中。印度刺猬蛋白/甲状旁腺激素相关蛋白信号系统在肥大软骨细胞和成骨软骨膜细胞的分化控制及相互作用中肯定起着重要作用。我们提出,所有早期肥大软骨细胞都具有分化为成骨样细胞并有助于初始骨形成的内在潜力,但只有位于软骨和(非软骨)成骨组织之间“边界地带”的软骨细胞才会进一步分化为产骨细胞。我们将这些肥大软骨细胞称为“边缘软骨细胞”,以强调它们的特定位置和双重分化潜力。位于不同软骨区域的肥大软骨细胞暴露于不合适的基质和内分泌/旁分泌环境中,无法分化为成骨样细胞,因此会发生凋亡。

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