Gassner K M, Tassava R A
Department of Molecular Genetics, Ohio State University, Columbus 43210, USA.
J Exp Zool. 1997 Dec 15;279(6):571-8.
Limb regeneration in the short-toes axolotl is impaired. Our goal was to characterize the regeneration process in this mutant by histological and immunocytochemical methods. Previous research indicates that age and a defective basement membrane may be instrumental factors in short-toes axolotl regeneration (Del Rio-Tsonis et al. [1992] Proc. Natl. Acad. Sci. U.S.A., 89:5502-5506). The present results show that limb regeneration can occur even in older (1-2-year-old) short-toes axolotls. The process was always significantly delayed, but the time required for complete regeneration varied. Even so, the basement membrane of short-toes regenerates showed no differences in thickness or shape compared with wild-type regenerates. Distally amputated short-toes limbs gave rise to more digits in the regenerate, indicating that regeneration may be somewhat dependent on the level of amputation. Since extracellular matrix (ECM) remodeling occurs extensively during regeneration, we compared the ECM of the short-toes and wild-type regenerates using monoclonal antibodies (mAbs) MT2 and ST1 (Tassava et al. [1996] Wound Rep. Reg., 4:75-81). The short-toes regenerates showed decreased reactivity to mAb MT2, which identifies type XII collagen, an ECM protein that is normally unregulated during regeneration, and increased reactivity to mAb ST1, which identifies a limb ECM component that typically undergoes breakdown in the distal stump. Thus, impaired regeneration in the short-toes axolotl is correlated with impaired ECM remodeling in the distal limb stump. This supports the view that ECM remodeling plays an important role in regeneration.
短趾蝾螈的肢体再生能力受损。我们的目标是通过组织学和免疫细胞化学方法来描述这种突变体的再生过程。先前的研究表明,年龄和有缺陷的基底膜可能是短趾蝾螈再生的重要因素(德尔里奥 - 索尼斯等人,[1992]《美国国家科学院院刊》,89:5502 - 5506)。目前的结果表明,即使是年龄较大(1 - 2岁)的短趾蝾螈也能发生肢体再生。这个过程总是明显延迟,但完全再生所需的时间各不相同。即便如此,短趾蝾螈再生肢体的基底膜与野生型再生肢体相比,在厚度或形状上并无差异。短趾蝾螈肢体远端截肢后,再生肢体中长出的指(趾)更多,这表明再生可能在一定程度上取决于截肢的水平。由于细胞外基质(ECM)重塑在再生过程中广泛发生,我们使用单克隆抗体(mAb)MT2和ST1比较了短趾蝾螈和野生型再生肢体的ECM(塔萨瓦等人,[1996]《伤口修复与再生》,4:75 - 81)。短趾蝾螈再生肢体对识别XII型胶原蛋白的mAb MT2的反应性降低,XII型胶原蛋白是一种在再生过程中通常不受调控的ECM蛋白,而对识别一种通常在远端残端会发生分解的肢体ECM成分的mAb ST1的反应性增加。因此,短趾蝾螈再生能力受损与肢体远端残端的ECM重塑受损相关。这支持了ECM重塑在再生中起重要作用的观点。