Suppr超能文献

间充质干细胞:21世纪分子医学的基石。

Mesenchymal stem cells: building blocks for molecular medicine in the 21st century.

作者信息

Caplan A I, Bruder S P

机构信息

Dept of Biology, Skeletal Research Center, Case Western Reserve University, Cleveland, OH, USA.

出版信息

Trends Mol Med. 2001 Jun;7(6):259-64. doi: 10.1016/s1471-4914(01)02016-0.

Abstract

Mesenchymal stem sells (MSCs) are present in a variety of tissues during human development, and in adults they are prevalent in bone marrow. From that readily available source, MSCs can be isolated, expanded in culture, and stimulated to differentiate into bone, cartilage, muscle, marrow stroma, tendon, fat and a variety of other connective tissues. Because large numbers of MSCs can be generated in culture, tissue-engineered constructs principally composed of these cells could be re-introduced into the in vivo setting. This approach is now being explored to regenerate tissues that the body cannot naturally repair or regenerate when challenged. Moreover, MSCs can be transduced with retroviral and other vectors and are, thus, potential candidates to deliver somatic gene therapies for local or systemic pathologies. Untapped applications include both diagnostic and prognostic uses of MSCs and their descendents in healthcare management. Finally, by understanding the complex, multistep and multifactorial differentiation pathway from MSC to functional tissues, it might be possible to manipulate MSCs directly in vivo to cue the formation of elaborate, composite tissues in situ.

摘要

间充质干细胞(MSCs)在人类发育过程中存在于多种组织中,在成人中它们在骨髓中普遍存在。从这个容易获得的来源,可以分离出MSCs,在培养中进行扩增,并刺激其分化为骨、软骨、肌肉、骨髓基质、肌腱、脂肪和各种其他结缔组织。由于可以在培养中产生大量的MSCs,主要由这些细胞组成的组织工程构建体可以重新引入体内环境。目前正在探索这种方法来再生身体在受到挑战时无法自然修复或再生的组织。此外,MSCs可以用逆转录病毒和其他载体进行转导,因此是为局部或全身性疾病提供体细胞基因治疗的潜在候选者。未开发的应用包括MSCs及其后代在医疗管理中的诊断和预后用途。最后,通过了解从MSCs到功能组织的复杂、多步骤和多因素分化途径,有可能直接在体内操纵MSCs以促使原位形成精细的复合组织。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验