Muschler George F, Nakamoto Chizu, Griffith Linda G
Departments of Orthopaedic Surgery and Biomedical Engineering (A41), The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
J Bone Joint Surg Am. 2004 Jul;86(7):1541-58. doi: 10.2106/00004623-200407000-00029.
Tissue engineering is a rapidly evolving discipline that seeks to repair, replace, or regenerate specific tissues or organs by translating fundamental knowledge in physics, chemistry, and biology into practical and effective materials, devices, systems, and clinical strategies. Stem cells and progenitors that are capable of forming new tissue with one or more connective tissue phenotypes are available from many adult tissues and are defined as connective tissue progenitors. There are four major cell-based tissue-engineering strategies: (1) targeting local connective tissue progenitors where new tissue is desired, (2) transplanting autogenous connective tissue progenitors, (3) transplanting culture-expanded or modified connective tissue progenitors, and (4) transplanting fully formed tissue generated in vitro or in vivo. Stem cell function is controlled by changes in stem cell activation and self-renewal or by changes in the proliferation, migration, differentiation, or survival of the progeny of stem cell activation, the downstream progenitor cells. Three-dimensional porous scaffolds promote new tissue formation by providing a surface and void volume that promotes the attachment, migration, proliferation, and desired differentiation of connective tissue progenitors throughout the region where new tissue is needed. Critical variables in scaffold design and function include the bulk material or materials from which it is made, the three-dimensional architecture, the surface chemistry, the mechanical properties, the initial environment in the area of the scaffold, and the late scaffold environment, which is often determined by degradation characteristics. Local presentation or delivery of bioactive molecules can change the function of connective tissue progenitors (activation, proliferation, migration, differentiation, or survival) in a manner that results in new or enhanced local tissue formation. All cells require access to substrate molecules (oxygen, glucose, and amino acids). A balance between consumption and local delivery of these substrates is needed if cells are to survive. Transplanted cells are particularly vulnerable. Theoretical calculations can be used to explore the relationships among cell density, diffusion distance, and cell viability within a graft and to design improved strategies for transplantation of connective tissue progenitors. Rational strategies for tissue engineering seek to optimize new tissue formation through the logical selection of conditions that modulate the performance of connective tissue progenitors in a graft site to produce a desired tissue. This increasingly involves strategies that combine cells, matrices, inductive stimuli, and techniques that enhance the survival and performance of local or transplanted connective tissue progenitors.
组织工程学是一门快速发展的学科,它试图通过将物理、化学和生物学的基础知识转化为实用且有效的材料、装置、系统及临床策略,来修复、替换或再生特定的组织或器官。能够形成具有一种或多种结缔组织表型的新组织的干细胞和祖细胞可从许多成体组织中获取,它们被定义为结缔组织祖细胞。基于细胞的组织工程学主要有四种策略:(1)在需要新组织的部位靶向局部结缔组织祖细胞;(2)移植自体结缔组织祖细胞;(3)移植经培养扩增或修饰的结缔组织祖细胞;(4)移植在体外或体内生成的完全形成的组织。干细胞功能受干细胞激活和自我更新的变化控制,或者受干细胞激活的子代(下游祖细胞)的增殖、迁移、分化或存活变化的控制。三维多孔支架通过提供一个表面和孔隙体积来促进新组织形成,该表面和孔隙体积可促进结缔组织祖细胞在需要新组织的整个区域的附着、迁移、增殖及所需的分化。支架设计和功能的关键变量包括其所用的主体材料、三维结构、表面化学性质、机械性能、支架区域的初始环境以及后期支架环境,后期支架环境通常由降解特性决定。生物活性分子的局部呈现或递送能够以导致新组织形成或增强局部组织形成的方式改变结缔组织祖细胞的功能(激活、增殖、迁移、分化或存活)。所有细胞都需要获取底物分子(氧气、葡萄糖和氨基酸)。如果细胞要存活,就需要在这些底物的消耗和局部递送之间保持平衡。移植的细胞尤其脆弱。理论计算可用于探索移植物内细胞密度、扩散距离和细胞活力之间的关系,并设计改进的结缔组织祖细胞移植策略。合理的组织工程学策略旨在通过合理选择条件来优化新组织形成,这些条件可调节结缔组织祖细胞在移植部位的性能,以产生所需的组织。这越来越多地涉及将细胞、基质、诱导刺激以及增强局部或移植的结缔组织祖细胞存活和性能的技术相结合的策略。