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股骨头骨骺滑脱中的基因表达。激光捕获显微切割及定量逆转录-聚合酶链反应评估

Gene expression in slipped capital femoral epiphysis. Evaluation with laser capture microdissection and quantitative reverse transcription-polymerase chain reaction.

作者信息

Scharschmidt Thomas, Jacquet Robin, Weiner Dennis, Lowder Elizabeth, Schrickel Tyson, Landis William J

机构信息

Northeastern Ohio Universities Colleges of Medicine and Pharmacy, Rootstown, Ohio, USA.

出版信息

J Bone Joint Surg Am. 2009 Feb;91(2):366-77. doi: 10.2106/JBJS.G.00039.

Abstract

BACKGROUND

Slipped capital femoral epiphysis is a poorly understood condition affecting adolescents. Prior studies have suggested that the etiology may be related to abnormal collagen in the growth plate cartilage, but we are not aware of any investigations analyzing collagen or other structural proteins on a molecular level in the affected tissue. This study was performed to evaluate expression of mRNA for key structural molecules in growth plate chondrocytes of patients with slipped capital femoral epiphysis.

METHODS

A core biopsy of the proximal femoral physis was performed in nine patients with slipped capital femoral epiphysis, and the specimens were compared with five specimens from the normal distal femoral and proximal tibial and fibular physes of age-matched patients treated surgically for a limb-length inequality. We utilized laser capture microdissection techniques followed by quantitative reverse transcription-polymerase chain reaction analysis to determine if a change or abnormality in type-II-collagen and/or aggrecan gene expression may be associated with slipped capital femoral epiphysis. With these techniques, we correlated chondrocyte spatial location and gene expression to provide greater insight into this pathological condition and a more complete understanding of growth plate biology in general.

RESULTS

Downregulation of both type-II collagen and aggrecan was found in the growth plates of the subjects with slipped capital femoral epiphysis when compared with the levels in the age-matched controls. In eight specimens from affected patients, the level of expression of type-II-collagen mRNA was, on the average (and standard error of the mean), 13.7% +/- 0.2% of that in four control specimens and the aggrecan level averaged only 26% +/- 0.2% of the control aggrecan level.

CONCLUSIONS

The decreases that we identified in type-II-collagen and aggrecan expression would affect the quantity, distribution, and organization of both components in a growth plate, but these changes could be associated with either the cause or the result of a slipped capital femoral epiphysis.

摘要

背景

股骨头骨骺滑脱是一种影响青少年但了解甚少的病症。既往研究表明,其病因可能与生长板软骨中胶原蛋白异常有关,但我们尚未知晓有任何研究在分子水平上分析受累组织中的胶原蛋白或其他结构蛋白。本研究旨在评估股骨头骨骺滑脱患者生长板软骨细胞中关键结构分子的mRNA表达。

方法

对9例股骨头骨骺滑脱患者进行股骨近端骨骺的核心活检,并将标本与5例因肢体长度不等接受手术治疗的年龄匹配患者的正常股骨远端、胫骨近端和腓骨近端骨骺标本进行比较。我们采用激光捕获显微切割技术,随后进行定量逆转录-聚合酶链反应分析,以确定II型胶原蛋白和/或聚集蛋白聚糖基因表达的变化或异常是否可能与股骨头骨骺滑脱有关。通过这些技术,我们将软骨细胞的空间位置与基因表达相关联,以更深入地了解这种病理状况,并更全面地了解生长板生物学。

结果

与年龄匹配的对照组相比,股骨头骨骺滑脱患者生长板中II型胶原蛋白和聚集蛋白聚糖均下调。在8例受累患者的标本中,II型胶原蛋白mRNA的平均表达水平(及平均标准误差)为4例对照标本的13.7%±0.2%,聚集蛋白聚糖水平平均仅为对照聚集蛋白聚糖水平的26%±0.2%。

结论

我们所确定的II型胶原蛋白和聚集蛋白聚糖表达的降低会影响生长板中这两种成分的数量、分布和组织,但这些变化可能与股骨头骨骺滑脱的病因或结果有关。

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