Galgaro Bruna C, Beckenkamp Liziane R, van den M Nunnenkamp Martha, Korb Vitória G, Naasani Liliana I S, Roszek Katarzyna, Wink Márcia R
Laboratório de Biologia Celular, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.
Department of Biochemistry, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University, Toruń, Poland.
Med Res Rev. 2021 Jul;41(4):2316-2349. doi: 10.1002/med.21796. Epub 2021 Mar 1.
Mesenchymal stem cells (MSCs) play an important role in tissue homeostasis and damage repair through their ability to differentiate into cells of different tissues, trophic support, and immunomodulation. These properties made them attractive for clinical applications in regenerative medicine, immune disorders, and cell transplantation. However, despite multiple preclinical and clinical studies demonstrating beneficial effects of MSCs, their native identity and mechanisms of action remain inconclusive. Since its discovery, the CD73/ecto-5'-nucleotidase is known as a classic marker for MSCs, but its role goes far beyond a phenotypic characterization antigen. CD73 contributes to adenosine production, therefore, is an essential component of purinergic signaling, a pathway composed of different nucleotides and nucleosides, which concentrations are finely regulated by the ectoenzymes and receptors. Thus, purinergic signaling controls pathophysiological functions such as proliferation, migration, cell fate, and immune responses. Despite the remarkable progress already achieved in considering adenosinergic pathway as a therapeutic target in different pathologies, its role is not fully explored in the context of the therapeutic functions of MSCs. Therefore, in this review, we provide an overview of the role of CD73 and adenosine-mediated signaling in the functions ascribed to MSCs, such as homing and proliferation, cell differentiation, and immunomodulation. Additionally, we will discuss the pathophysiological role of MSCs, via CD73 and adenosine, in different diseases, as well as in tumor development and progression. A better understanding of the adenosinergic pathway in the regulation of MSCs functions will help to provide improved therapeutic strategies applicable in regenerative medicine.
间充质干细胞(MSCs)通过其分化为不同组织细胞的能力、营养支持和免疫调节作用,在组织稳态和损伤修复中发挥着重要作用。这些特性使其在再生医学、免疫紊乱和细胞移植的临床应用中具有吸引力。然而,尽管多项临床前和临床研究证明了MSCs的有益作用,但其天然特性和作用机制仍不明确。自发现以来,CD73/胞外5'-核苷酸酶一直被认为是MSCs的经典标志物,但其作用远不止于表型特征抗原。CD73有助于腺苷的产生,因此是嘌呤能信号传导的重要组成部分,嘌呤能信号传导是一条由不同核苷酸和核苷组成的途径,其浓度由胞外酶和受体精细调节。因此,嘌呤能信号传导控制着诸如增殖、迁移、细胞命运和免疫反应等病理生理功能。尽管在将腺苷能途径作为不同疾病的治疗靶点方面已经取得了显著进展,但其在MSCs治疗功能方面的作用尚未得到充分探索。因此,在本综述中,我们概述了CD73和腺苷介导的信号传导在MSCs的归巢和增殖、细胞分化及免疫调节等功能中的作用。此外,我们还将讨论MSCs通过CD73和腺苷在不同疾病以及肿瘤发生发展中的病理生理作用。更好地理解腺苷能途径在MSCs功能调节中的作用,将有助于提供适用于再生医学的改进治疗策略。