Lévesque Mathieu, Gatien Samuel, Finnson Kenneth, Desmeules Sophie, Villiard Eric, Pilote Mireille, Philip Anie, Roy Stéphane
Department of Biochemistry, Université de Montréal, Montréal, Québec, Canada.
PLoS One. 2007 Nov 28;2(11):e1227. doi: 10.1371/journal.pone.0001227.
Axolotls (urodele amphibians) have the unique ability, among vertebrates, to perfectly regenerate many parts of their body including limbs, tail, jaw and spinal cord following injury or amputation. The axolotl limb is the most widely used structure as an experimental model to study tissue regeneration. The process is well characterized, requiring multiple cellular and molecular mechanisms. The preparation phase represents the first part of the regeneration process which includes wound healing, cellular migration, dedifferentiation and proliferation. The redevelopment phase represents the second part when dedifferentiated cells stop proliferating and redifferentiate to give rise to all missing structures. In the axolotl, when a limb is amputated, the missing or wounded part is regenerated perfectly without scar formation between the stump and the regenerated structure. Multiple authors have recently highlighted the similarities between the early phases of mammalian wound healing and urodele limb regeneration. In mammals, one very important family of growth factors implicated in the control of almost all aspects of wound healing is the transforming growth factor-beta family (TGF-beta). In the present study, the full length sequence of the axolotl TGF-beta1 cDNA was isolated. The spatio-temporal expression pattern of TGF-beta1 in regenerating limbs shows that this gene is up-regulated during the preparation phase of regeneration. Our results also demonstrate the presence of multiple components of the TGF-beta signaling machinery in axolotl cells. By using a specific pharmacological inhibitor of TGF-beta type I receptor, SB-431542, we show that TGF-beta signaling is required for axolotl limb regeneration. Treatment of regenerating limbs with SB-431542 reveals that cellular proliferation during limb regeneration as well as the expression of genes directly dependent on TGF-beta signaling are down-regulated. These data directly implicate TGF-beta signaling in the initiation and control of the regeneration process in axolotls.
美西螈(有尾两栖动物)在脊椎动物中具有独特的能力,能够在受伤或截肢后完美地再生身体的许多部位,包括四肢、尾巴、颌骨和脊髓。美西螈的四肢是研究组织再生时使用最广泛的结构作为实验模型。这个过程具有良好的特征,需要多种细胞和分子机制。准备阶段是再生过程的第一部分,包括伤口愈合、细胞迁移、去分化和增殖。重新发育阶段是第二部分,去分化细胞停止增殖并重新分化以产生所有缺失的结构。在美西螈中,当四肢被截肢时,缺失或受伤的部分会完美再生,残端和再生结构之间不会形成疤痕。最近有多位作者强调了哺乳动物伤口愈合早期阶段与有尾两栖动物肢体再生之间的相似性。在哺乳动物中,参与控制伤口愈合几乎所有方面的一个非常重要的生长因子家族是转化生长因子-β家族(TGF-β)。在本研究中,分离出了美西螈TGF-β1 cDNA的全长序列。TGF-β1在再生四肢中的时空表达模式表明,该基因在再生的准备阶段被上调。我们的结果还证明了美西螈细胞中存在TGF-β信号传导机制的多个成分。通过使用TGF-β I型受体的特异性药理抑制剂SB-431542,我们表明TGF-β信号传导是美西螈肢体再生所必需的。用SB-431542处理再生四肢发现,肢体再生过程中的细胞增殖以及直接依赖于TGF-β信号传导的基因表达均下调。这些数据直接表明TGF-β信号传导在美西螈再生过程的启动和控制中起作用。