Godwin James W, Pinto Alexander R, Rosenthal Nadia A
The Jackson Laboratory, Bar Harbor, ME, 04609, USA; MDI Biological Laboratory, Salisbury Cove, ME 04672, USA; Australian Regenerative Medicine Institute, Monash University, Victoria, 3800, Australia.
The Jackson Laboratory, Bar Harbor, ME, 04609, USA.
Semin Cell Dev Biol. 2017 Jan;61:71-79. doi: 10.1016/j.semcdb.2016.08.008. Epub 2016 Aug 10.
Identification of the key ingredients and essential processes required to achieve perfect tissue regeneration in humans has so far remained elusive. Injury in vertebrates induces an obligatory wound response that will precede or overlap any regeneration specific program or scarring outcome. This process shapes the cellular and molecular landscape of the tissue, influencing the success of endogenous repair pathways or for potential clinical intervention. The involvement of immune cells is also required for aspects of development extending beyond the initial inflammatory phase of wounding. It has now become clear from amphibian, fish and mammalian models of tissue injury that the type of immune response and the profile of immune cells attending the site of injury can act as the gatekeepers that determine wound repair quality. The heterogeneity among innate and adaptive immune cell populations, along with the developmental origin of these cells, form key ingredients affecting the potential for downstream repair and the suppression of fibrosis. Cell-to-cell interactions between immune cells, such as macrophages and T cells, with stem cells and mesenchymal cells are critically important for shaping this process and these exchanges, are in turn influenced by the type of injury, tissue location and developmental stage of the organism. Developmentally, mouse cardiac regeneration is restricted to early stages of postnatal life where the balance of innate to adaptive immune cells may be poised towards regeneration. In the injured adult mouse liver, specific macrophage subsets improve repair while other bone marrow derived cells can exacerbate injury. Other studies using genetically diverse mice have shown enhanced regeneration in certain strains, restricted to specific tissues. This enhanced repair is linked with expression of genes such as Insulin-like Growth Factor- 1 (IGF-1) and activin (Act 1), that both play important roles in shaping the immune system. Immune cells are now appreciated to have powerful influences on critical cell types required for regeneration success. The winning recipe for tissue regeneration is likely to be found ultimately by identifying the genetic elements and specific cell populations that limit or allow intrinsic potential. This will be essential for developing therapeutic strategies for tissue regeneration in humans.
迄今为止,要确定实现人体完美组织再生所需的关键成分和基本过程仍然困难重重。脊椎动物受伤后会引发一种强制性的伤口反应,这种反应会先于任何再生特异性程序或瘢痕形成结果出现,或者与之重叠。这个过程塑造了组织的细胞和分子格局,影响内源性修复途径的成功与否或潜在临床干预的效果。除了伤口最初的炎症阶段之外,免疫细胞的参与对于发育的各个方面也是必需的。现在,从两栖动物、鱼类和哺乳动物的组织损伤模型中可以清楚地看到,免疫反应的类型以及聚集在损伤部位的免疫细胞谱可以充当决定伤口修复质量的守门人。先天免疫细胞群体和适应性免疫细胞群体之间的异质性,以及这些细胞的发育起源,构成了影响下游修复潜力和纤维化抑制的关键因素。免疫细胞之间的细胞间相互作用,如巨噬细胞和T细胞与干细胞和间充质细胞之间的相互作用,对于塑造这个过程至关重要,而这些相互作用又反过来受到损伤类型、组织位置和生物体发育阶段的影响。在发育过程中,小鼠心脏再生仅限于出生后的早期阶段,此时先天免疫细胞与适应性免疫细胞的平衡可能有利于再生。在成年小鼠肝脏损伤模型中,特定的巨噬细胞亚群可改善修复,而其他骨髓来源的细胞则可能加剧损伤。其他使用基因多样化小鼠的研究表明,某些品系在特定组织中再生能力增强。这种增强的修复与胰岛素样生长因子-1(IGF-1)和激活素(Act 1)等基因的表达有关,这些基因在塑造免疫系统方面都发挥着重要作用。现在人们认识到免疫细胞对再生成功所需的关键细胞类型有强大影响。最终,可能通过确定限制或允许内在潜力的遗传因素和特定细胞群体来找到组织再生的成功秘诀。这对于开发人类组织再生的治疗策略至关重要。