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成人耳软骨膜中软骨祖细胞的鉴定:用于软骨重建

Identification of cartilage progenitor cells in the adult ear perichondrium: utilization for cartilage reconstruction.

作者信息

Togo Takeshi, Utani Atsushi, Naitoh Motoko, Ohta Masayoshi, Tsuji Yasumi, Morikawa Noriyuki, Nakamura Motonobu, Suzuki Shigehiko

机构信息

Department of Plastic and Reconstructive Surgery, Kyoto University Graduate School of Medicine, Sakyo-Ku, Kyoto, Japan.

出版信息

Lab Invest. 2006 May;86(5):445-57. doi: 10.1038/labinvest.3700409.

Abstract

For cartilage reconstruction, it is still difficult to obtain a sufficient volume of cartilage and to maintain its functional phenotype for a long period. Utilizing tissue stem cells is one approach to overcome such difficulties. We show here the presence of cartilage progenitor cells in the ear perichondrium of adult rabbits by 5-bromo-2'-deoxyuridine labeling, clonogenicity, and differentiation analyses. Long-term label-retaining cells were demonstrated in the perichondrium. Cells from the perichondrium, that is, perichondrocytes were mechanically isolated using a raspatory and maintained in D-MEM/F-12 medium with 10% FCS. They proliferated more vigorously than chondrocytes from the cartilage. Perichondrocytes could differentiate into adipocytes as well as osteocytes in differentiation induction medium. For cartilage reconstruction in vivo, perichondrocytes were seeded on collagen sponge scaffolds and implanted in nude mice. After 4 weeks, the composites with perichondrocytes generated the same weight of cartilaginous tissue as those with chondrocytes. They produced glycosaminoglycan and type II collagen as shown by RT-PCR and immunohistochemical examination. On the contrary, rabbit bone marrow mesenchymal stem cells used as control could regenerate significantly smaller cartilage than perichondrocytes in the implant study. Based on these findings, we propose that the perichondrium containing tissue progenitor cells is one of the potential candidates for use in reconstructing cartilage and new therapeutic modalities.

摘要

对于软骨重建而言,获取足够体积的软骨并长期维持其功能表型仍然具有挑战性。利用组织干细胞是克服这些困难的一种方法。我们通过5-溴-2'-脱氧尿苷标记、克隆形成能力和分化分析,证明成年兔耳软骨膜中存在软骨祖细胞。在软骨膜中发现了长期标记保留细胞。使用刮匙机械分离软骨膜细胞,即软骨膜细胞,并将其置于含有10%胎牛血清的D-MEM/F-12培养基中培养。它们比软骨中的软骨细胞增殖更旺盛。在分化诱导培养基中,软骨膜细胞可分化为脂肪细胞和骨细胞。为了进行体内软骨重建,将软骨膜细胞接种在胶原海绵支架上并植入裸鼠体内。4周后,含有软骨膜细胞的复合物产生的软骨组织重量与含有软骨细胞的复合物相同。逆转录-聚合酶链反应(RT-PCR)和免疫组织化学检查显示,它们产生了糖胺聚糖和II型胶原。相反,在植入研究中,用作对照的兔骨髓间充质干细胞再生的软骨明显小于软骨膜细胞。基于这些发现,我们提出,含有组织祖细胞的软骨膜是用于软骨重建和新治疗模式的潜在候选物之一。

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