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转化生长因子-β1在新鲜移植至关节软骨全层缺损处的生长板中的免疫组织化学定位

[Immunohistochemical localization of transforming growth factor-beta 1 in growth plate freshly transplanted into a full-thickness defect in articular cartilage].

作者信息

Umehara T

机构信息

Department of Orthopedic Surgery, School of Medicine, University of Tokushima, Japan.

出版信息

Nihon Seikeigeka Gakkai Zasshi. 1994 Sep;68(9):790-7.

PMID:7525796
Abstract

Transplants of the epiphyseal growth plate obtained from the proximal tibia of Lewis rats at 3 weeks of age were inserted into full-thickness defects in the patellofemoral articular surface of Lewis rats at 5 weeks of age. As controls, similar surface defects were induced but no transplants were inserted. Transplants were studied immunohistochemically at varying intervals up to 72 weeks in order to determine the effects of transforming growth factor-beta 1 (TGF-beta 1) on the repair of the articular cartilage by the epiphyseal growth plate. TGF-beta 1 was present in chondrocytes in the region corresponding to the hypertrophic zone of the transplanted growth plate at 1 week after transplantation. The distribution pattern of TGF-beta 1 in this hypertrophic zone was similar to that prior to transplantation. At 2 weeks after transplantation, TGF-beta 1 was detected in the matrix, but the hypertrophic chondrocyte cell membranes were not clear. TGF-beta 1 was undetectable in the transplanted growth plate at 4 weeks after transplantation, at which time a morphological examination revealed metaplastically-transformed articular cartilage but no hypertrophic cartilage cells. No immunostaining of TGF-beta 1 was present in the untreated articular defect. These findings suggested that TGF-beta 1 in the hypertrophic chondrocytes was probably transferred from the cytoplasm to the extracellular matrix and stimulated the ossification of the matrix with vessel induction and osteoid formation during the process of incorporation of the transplant into the articular cartilage defect.

摘要

将3周龄Lewis大鼠胫骨近端获取的骺生长板移植到5周龄Lewis大鼠髌股关节面的全层缺损处。作为对照,诱导产生类似的表面缺损但不植入移植组织。对移植组织进行免疫组织化学研究,时间间隔最长至72周,以确定转化生长因子-β1(TGF-β1)对骺生长板修复关节软骨的影响。移植后1周,在移植生长板对应肥大带区域的软骨细胞中存在TGF-β1。该肥大带中TGF-β1的分布模式与移植前相似。移植后2周,在基质中检测到TGF-β1,但肥大软骨细胞膜不清晰。移植后4周,在移植的生长板中未检测到TGF-β1,此时形态学检查显示为化生转化的关节软骨,但无肥大软骨细胞。未处理的关节缺损处未出现TGF-β1免疫染色。这些发现表明,肥大软骨细胞中的TGF-β1可能从细胞质转移到细胞外基质,并在移植组织融入关节软骨缺损的过程中,通过诱导血管生成和类骨质形成来刺激基质的骨化。

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