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兔股骨远端软骨骨骺在次级骨化中心发育过程中的血管生成。

Angiogenesis in the distal femoral chondroepiphysis of the rabbit during development of the secondary centre of ossification.

作者信息

Doschak M R, Cooper D M L, Huculak C N, Matyas J R, Hart D A, Hallgrimsson B, Zernicke R F, Bray R C

机构信息

Department of Surgery, McCaig Centre for Joint Injury and Arthritis Research, Faculty of Medicine, University of Calgary, Alberta, Canada.

出版信息

J Anat. 2003 Aug;203(2):223-33. doi: 10.1046/j.1469-7580.2003.00198.x.

Abstract

In the developing chondroepiphyses of long bones, the avascular cartilaginous anlage is invaded by numerous blood vessels, through the process of angiogenesis. The objective of this study was to investigate the chronology of this vascular invasion with the spontaneous calcification of the cartilaginous epiphysis during development of the secondary ossification centre in the rabbit distal femur. The time-course of chondroepiphyseal vascular invasion was determined histologically and standardized for eight gestational and four postnatal intervals by plotting kit body mass against crown-rump length. Similarly, microcomputed tomography (micro-CT) helped to visualize calcification at those same gestational and postnatal intervals. To confirm the angiogenic nature of the avascular chondroepiphysis, such samples were assayed on the chick chorio-allantoic membrane (CAM). Neovascular outgrowths from the CAM were apparent 48 h following introduction of an 18-day (gestational) chondroepiphyseal sample. Chondroepiphyseal samples were assayed for the potent developmental angiogenic factors bFGF and VEGF, with the mRNA expression for both these mediators being confirmed using RT-PCR. As angiogenesis and calcification during chondroepiphyseal development occur in a defined tissue environment initially devoid of blood vessels and mineral, those processes provided a unique opportunity to study their progression without complication of injury-related inflammation or extant vasculature and mineral. Furthermore, the discovery of angiogenic, angiostatic or mineral-regulating mediators specific to developing connective tissue may prove useful for analysing the regulation of vascular and mineral pathogenesis in articular tissues.

摘要

在长骨发育中的软骨骨骺中,无血管的软骨原基通过血管生成过程被大量血管侵入。本研究的目的是研究在兔股骨远端次级骨化中心发育过程中,这种血管侵入与软骨骨骺自发钙化的时间顺序。通过绘制试剂盒体重与顶臀长度的关系图,从组织学上确定软骨骨骺血管侵入的时间进程,并将其标准化为八个孕期和四个出生后间隔。同样,显微计算机断层扫描(micro-CT)有助于观察相同孕期和出生后间隔的钙化情况。为了证实无血管软骨骨骺的血管生成性质,将此类样本在鸡胚绒毛尿囊膜(CAM)上进行检测。在引入18天(孕期)的软骨骨骺样本后48小时,CAM上出现了新生血管生长。对软骨骨骺样本检测了强效发育血管生成因子bFGF和VEGF,并使用RT-PCR确认了这两种介质的mRNA表达。由于软骨骨骺发育过程中的血管生成和钙化发生在最初无血管和矿物质的特定组织环境中,这些过程提供了一个独特的机会来研究它们的进展,而不会受到损伤相关炎症或现有血管和矿物质的干扰。此外,发现特定于发育中结缔组织的血管生成、血管抑制或矿物质调节介质可能有助于分析关节组织中血管和矿物质发病机制的调节。

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