Amiel D, Nagineni C N, Choi S H, Lee J
Department of Orthopaedics, University of California San Diego, La Jolla 92093-0630, USA.
Med Sci Sports Exerc. 1995 Jun;27(6):844-51.
Different intrinsic properties of the constituent cells of the anterior cruciate ligament (ACL) and medial collateral ligament (MCL) have been proposed to be one of the factors in the differential repair mechanisms. We have found that the outgrowth of cells from rabbit ACL explants was slower than from MCL explants after 10 d. Growth curves of ACL and MCL cultures at both Passage numbers 2 and 6 showed a slower rate of proliferation of ACL cells than MCL cells (P < 0.005). The proliferative response of rabbit ACL and MCL cells to b-FGF and TGF-beta was also investigated. Both b-FGF and TGF-beta had no significant effect on cell proliferation of ACL and MCL cultures after 48 h. However, TGF-beta did have an inhibitory effect on thymidine incorporation, especially at concentrations greater than 1 ng.ml-1, while b-FGF stimulated thymidine incorporation in ACL and MCL in a dose-dependent manner. Differences in the cell morphology of the ACL and MCL cells grown in culture were seen also. Cells from Passages 3-6 demonstrated these differences more prominently, and phalloidin staining for actin showed that ACL cells appeared to have more intracellular actin fibers.
前交叉韧带(ACL)和内侧副韧带(MCL)组成细胞的不同内在特性被认为是导致不同修复机制的因素之一。我们发现,10天后,兔ACL外植体的细胞生长速度比MCL外植体慢。第2代和第6代ACL和MCL培养物的生长曲线显示,ACL细胞的增殖速度比MCL细胞慢(P < 0.005)。我们还研究了兔ACL和MCL细胞对碱性成纤维细胞生长因子(b-FGF)和转化生长因子-β(TGF-β)的增殖反应。48小时后,b-FGF和TGF-β对ACL和MCL培养物的细胞增殖均无显著影响。然而,TGF-β对胸苷掺入有抑制作用,尤其是在浓度大于1 ng/ml时,而b-FGF以剂量依赖的方式刺激ACL和MCL中的胸苷掺入。培养的ACL和MCL细胞的形态也存在差异。第3 - 6代细胞的这些差异更为明显,肌动蛋白的鬼笔环肽染色显示ACL细胞似乎有更多的细胞内肌动蛋白纤维。