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具有多向分化能力的小鼠颞下颌关节盘细胞克隆的永生化及特性分析

Immortalization and characterization of mouse temporomandibular joint disc cell clones with capacity for multi-lineage differentiation.

作者信息

Park Y, Hosomichi J, Ge C, Xu J, Franceschi R, Kapila S

机构信息

Department of Orthodontics and Pediatric Dentistry, School of Dentistry, The University of Michigan, Ann Arbor, MI, USA.

Department of Orthodontics and Pediatric Dentistry, School of Dentistry, The University of Michigan, Ann Arbor, MI, USA; Department of Orthodontic Science, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Osteoarthritis Cartilage. 2015 Sep;23(9):1532-42. doi: 10.1016/j.joca.2015.04.006. Epub 2015 Apr 14.

Abstract

OBJECTIVE

Despite the importance of temporomandibular joint (TMJ) disc in normal function and disease, studying the responses of its cells has been complicated by the lack of adequate characterization of the cell subtypes. The purpose of our investigation was to immortalize, clone, characterize and determine the multi-lineage potential of mouse TMJ disc cells.

DESIGN

Cells from 12-week-old female mice were cultured and immortalized by stable transfection with human telomerase reverse transcriptase (hTERT). The immortalized cell clones were phenotyped for fibroblast- or chondrocyte-like characteristics and ability to undergo adipocytic, osteoblastic and chondrocytic differentiation.

RESULTS

Of 36 isolated clones, four demonstrated successful immortalization and maintenance of stable protein expression for up to 50 passages. Two clones each were initially characterized as fibroblast-like and chondrocyte-like on the basis of cell morphology and growth rate. Further the chondrocyte-like clones had higher mRNA expression levels of cartilage oligomeric matrix protein (COMP) (>3.5-fold), collagen X (>11-fold), collagen II expression (2-fold) and collagen II:I ratio than the fibroblast-like clones. In contrast, the fibroblast-like clones had higher mRNA expression level of vimentin (>1.5-fold), and fibroblastic specific protein 1 (>2.5-fold) than the chondrocyte-like clones. Both cell types retained multi-lineage potential as demonstrated by their capacity to undergo robust adipogenic, osteogenic and chondrogenic differentiation.

CONCLUSIONS

These studies are the first to immortalize TMJ disc cells and characterize chondrocyte-like and fibroblast-like clones with retained multi-differentiation potential that would be a valuable resource in studies to dissect the behavior of specific cell types in health and disease and for tissue engineering.

摘要

目的

尽管颞下颌关节(TMJ)盘在正常功能和疾病中具有重要作用,但由于缺乏对细胞亚型的充分表征,研究其细胞反应一直很复杂。我们研究的目的是使小鼠TMJ盘细胞永生化、克隆、表征并确定其多谱系潜能。

设计

培养来自12周龄雌性小鼠的细胞,并通过用人端粒酶逆转录酶(hTERT)进行稳定转染使其永生化。对永生化细胞克隆进行表型分析,以确定其成纤维细胞样或软骨细胞样特征以及进行脂肪形成、成骨和软骨形成分化的能力。

结果

在36个分离的克隆中,有4个显示成功永生化并维持稳定的蛋白质表达达50代。根据细胞形态和生长速率,最初将两个克隆分别表征为成纤维细胞样和软骨细胞样。此外,软骨细胞样克隆的软骨寡聚基质蛋白(COMP)(>3.5倍)、胶原蛋白X(>11倍)、胶原蛋白II表达(2倍)和胶原蛋白II:I比值的mRNA表达水平高于成纤维细胞样克隆。相反,成纤维细胞样克隆的波形蛋白(>1.5倍)和成纤维细胞特异性蛋白1(>2.5倍)的mRNA表达水平高于软骨细胞样克隆。两种细胞类型都保留了多谱系潜能,这通过它们进行强大的脂肪生成、成骨和软骨生成分化的能力得到证明。

结论

这些研究首次使TMJ盘细胞永生化,并表征了具有保留的多分化潜能的软骨细胞样和成纤维细胞样克隆,这将是研究健康和疾病中特定细胞类型行为以及组织工程的宝贵资源。

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