Cancedda Ranieri, Bollini Sveva, Descalzi Fiorella, Mastrogiacomo Maddalena, Tasso Roberta
Biorigen Srl, Genova, Italy.
Department of Experimental Medicine, University of Genova, Genova, Italy.
Front Bioeng Biotechnol. 2017 Apr 28;5:28. doi: 10.3389/fbioe.2017.00028. eCollection 2017.
For repair of chronic or difficult-to-heal tissue lesions and defects, major constraints exist to a broad application of cell therapy and tissue engineering approaches, i.e., transplantation of "" expanded autologous stem/progenitor cells, alone or associated with carrier biomaterials. To enable a large number of patients to benefit, new strategies should be considered. One of the main goals of contemporary regenerative medicine is to develop new regenerative therapies, inspired from Mother Nature. In all injured tissues, when platelets are activated by tissue contact, their released factors promote innate immune cell migration to the wound site. Platelet-derived factors and factors secreted by migrating immune cells create an inflammatory microenvironment, in turn, causing the activation of angiogenesis and vasculogenesis processes. Eventually, repair or regeneration of the injured tissue occurs paracrine signals activating, mobilizing or recruiting to the wound site cells with healing potential, such as stem cells, progenitors, or undifferentiated cells derived from the reprogramming of tissue differentiated cells. This review, largely based on our studies, discusses the identification of new tools, inspired by cellular and molecular mechanisms overseeing physiological tissue healing, that could reactivate dormant endogenous regeneration mechanisms lost during evolution and ontogenesis.
对于慢性或难以愈合的组织损伤和缺损的修复,细胞疗法和组织工程方法(即单独移植“扩增的自体干/祖细胞”或与载体生物材料联合移植)的广泛应用存在重大限制。为了使大量患者受益,应考虑新的策略。当代再生医学的主要目标之一是借鉴大自然的灵感开发新的再生疗法。在所有受伤组织中,当血小板通过与组织接触而被激活时,其释放的因子会促进先天免疫细胞向伤口部位迁移。血小板衍生因子和迁移的免疫细胞分泌的因子会形成一种炎症微环境,进而导致血管生成和血管发生过程的激活。最终,受伤组织通过旁分泌信号激活、动员或招募具有愈合潜力的细胞(如干细胞、祖细胞或由组织分化细胞重编程产生的未分化细胞)迁移到伤口部位,从而实现修复或再生。本综述主要基于我们的研究,讨论了受监督生理组织愈合的细胞和分子机制启发而发现的新工具,这些工具可以重新激活在进化和个体发育过程中丧失的休眠内源性再生机制。