干细胞概述:从不断发展的血液生物学概念到临床实践中的(自动)移植

B. Balint, M. Pavlovic, O. Markovic, S. Borović, M. Todorović
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摘要

常规的造血干细胞移植是一种众所周知的治疗许多获得性和先天性造血疾病、免疫系统疾病以及某些代谢疾病的方法。干细胞(SCs)可以被定义为具有自我更新能力的细胞,具有高增殖能力,并有可能分化为具有功能的成熟细胞。干细胞可分为胚胎干细胞(ESCs)和组织特异性或成体干细胞,如骨髓(BM)干细胞、外周血(PB)干细胞和来自脐带血(UCB)的SCs,以及其他非造血或体细胞SCs。成人的SCs通常被认为在再生和分化潜能方面受到限制,而胚胎干细胞是“真正的”全能/多能细胞,因为它们能够发育成内胚层、外胚层或中胚层——人体中所有三种胚胎组织类型。它们是最有前途的,但也是最具争议的可移植SCs类型。未成熟的造血SCs具有分化潜能,不仅可以分化为所有血细胞,还可以分化为某些体细胞类型(SC可塑性)。在不同的临床环境中,未成熟干细胞的移植会导致受体骨髓的再生,随后会有完整、稳定和长期的造血重建。考虑到未成熟干细胞也能够归巢到不同的组织,将自体干细胞植入受损和/或缺血区域可诱导其定植并连续转分化为宿主器官的细胞系,包括新生血管。因此,它们在再生医学领域具有临床应用价值,可用于治疗心肌、脑、血管、肝脏、胰腺等组织损伤。本综述的目的是概括快速发展的干细胞研究领域的关键进展,并回顾SCs在常规移植和再生医学中的应用。此外,将对我们自己的干细胞研究进行简要的批判性评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A stem cell overview: From evolving hemobiological concepts to (auto)grafting in clinical practice
Conventional hematopoietic stem cell transplantation is a well-known treatment method for numerous acquired and congenital hematopoietic disorders, disorders of the immune system, as well as certain metabolic disorders. Stem cells (SCs) can be defined as cells capable of self-renewal with a high proliferative capacity and the potential to differentiate into functionally competent mature cells. Stem cells can be divided into embryonic SCs (ESCs) and tissue-specific or adult SCs - such as bone marrow (BM) stem cells, peripheral blood (PB) stem cells, and SCs derived from umbilical cord blood (UCB), as well as other non-hematopoietic or somatic SCs. SCs in adults are characteristically considered to be restricted in their regenerative and differentiative potential, while embryonic stem cells are 'true' totipotent/pluripotent cells, due to their ability to develop into endoderm, ectoderm, or mesoderm - all three embryonic tissue types in the human body. They are the most promising, but also the most controversial type of potentially transplantable SCs. Immature hematopoietic SCs have the potential of differentiating, not only into all blood cells, but also into some somatic cell types (SC plasticity). In different clinical settings, the transplantation of immature stem cells leads to the repopulation of recipient bone marrow, with subsequent complete, stable, and long-term reconstitution of hematopoiesis. Given that immature stem cells are also capable of homing to different tissues, autologous stem cell implantation into a damaged and/or ischemic area induces their colonizing and consecutive transdifferentiating into cell lineages of the host organ, including neovascularization. Thus, they are clinically applicable in the field of regenerative medicine for the treatment of myocardial, brain, vascular, liver, pancreatic, and other tissue damage. The purpose of this overview is to recapitulate the key developments in the rapidly evolving area of stem cell research, as well as to review the use of SCs in conventional transplantations and in regenerative medicine. Additionally, a brief critical evaluation of our own stem cell research will be summarized.
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