Wu Ya Fang, Zhou You Lang, Mao Wei Feng, Avanessian Bella, Liu Paul Y, Tang Jin Bo
Hand Surgery Research Center, Department of Hand Surgery, Affiliated Hospital of Nantong University, Nantong, China.
J Hand Surg Am. 2012 Feb;37(2):209-16. doi: 10.1016/j.jhsa.2011.10.049. Epub 2011 Dec 29.
Cellular apoptosis might be an important molecular event in the middle or late healing periods of intrasynovial tendons, but this has not been studied. We aimed to investigate cellular apoptosis and corresponding cellular proliferation in the middle and late healing stages of intrasynovial tendons.
The flexor digitorum profundus tendons of 48 long toes (24 chickens) were completely transected within the sheath region and were repaired surgically. At days 28, 42, 56, and 84 after surgery, tendons were harvested and sectioned. In situ terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay was performed to detect apoptotic cells. The sections were stained immunofluorescently with antibodies to proliferating cell nuclear antigen to assess proliferation and to Bcl-2 (an anti-apoptotic protein). Positively stained tenocytes were counted, and their distributional differences were verified in 3-dimensional images.
The repaired intrasynovial tendons exhibited generally greater apoptosis in the surface region than in the core. The differences were more remarkable in the extended region than in the junction region of the cut tendon. At the core of the junction site, apoptosis of tenocytes was pronounced at all time points, but it was less severe at the core of the extended region. The proliferating cell nuclear antigen-positive and Bcl-2-positive tenocytes decreased significantly and continually at days 28, 42, and 56, respectively; these tenocytes were at a minimum at days 56 and 84.
Apoptotic changes of tenocytes are most marked in the surface region and in the junction region of the healing tendon in the middle and late healing stages. Apoptosis in the core is less dramatic compared to that in the surface in the extended tendon regions. Cellular proliferation declines drastically and is minimal at days 56 and 84.
Tenocyte apoptosis in the middle and late stages might be an important event contributing to intrasynovial tendon remodeling, which affects the healing strength and formation of adhesions.
细胞凋亡可能是滑膜内肌腱愈合中后期的一个重要分子事件,但尚未得到研究。我们旨在研究滑膜内肌腱愈合中后期的细胞凋亡及相应的细胞增殖情况。
将48只长趾(24只鸡)的指深屈肌腱在腱鞘区域完全横断并进行手术修复。术后第28、42、56和84天,采集肌腱并切片。采用原位末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)法检测凋亡细胞。切片用增殖细胞核抗原抗体进行免疫荧光染色以评估增殖情况,并用抗凋亡蛋白Bcl-2抗体进行染色。对阳性染色的腱细胞进行计数,并在三维图像中验证其分布差异。
修复后的滑膜内肌腱表面区域的凋亡通常比核心区域更明显。在切断肌腱的延伸区域,差异比在连接区域更显著。在连接部位的核心,腱细胞的凋亡在所有时间点都很明显,但在延伸区域的核心则较轻。增殖细胞核抗原阳性和Bcl-2阳性的腱细胞分别在第28、42和56天显著且持续减少;这些腱细胞在第56和84天最少。
在愈合中后期,腱细胞的凋亡变化在愈合肌腱的表面区域和连接区域最为明显。与延伸肌腱区域的表面相比,核心区域的凋亡不那么显著。细胞增殖在第56和84天急剧下降且最少。
中后期的腱细胞凋亡可能是导致滑膜内肌腱重塑的一个重要事件,这会影响愈合强度和粘连形成。