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组织因子基因敲除对脐带源多能间充质基质/干细胞凝血特性的影响

Impact of Tissue Factor Gene Knockout on Coagulation Properties of Umbilical Cord-Derived Multipotent Mesenchymal Stromal/Stem Cells.

作者信息

Heidari Zahra, Fallahi Jafar, Sisakht Mohsen, Safari Fatemeh, Hosseini Kamran, Bahmanimehr Ardeshir, Savardashtaki Amir, Khajeh Sahar, Tabei Seyed Mohammad Bagher, Razban Vahid

机构信息

Department of Molecular Medicine, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.

Diagnostic Laboratory Sciences and Technology Research Center, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Cell Biochem Funct. 2024 Dec;42(8):e70021. doi: 10.1002/cbf.70021.

Abstract

Multipotent mesenchymal stromal/stem cells (MSCs) refer to a population of stem cells that exhibit distinct progenitor cell characteristics including the potential for differentiation into a wide range of cell types. MSCs have become a promising candidate for cell therapy and tissue regeneration due to their unique properties, such as their ability to differentiate into multiple cell types, their capacity for expansion, self-renewal, and immune-regulatory effects. However, reports have brought attention to thrombosis-related complications associated with MSCs therapy in the last decade. As tissue factor (TF) is a powerful coagulation activator expressed by MSCs that stimulates the extrinsic coagulation pathway, we investigated the thrombotic properties of human umbilical cord MSCs (HUCMSCs) after knocking out the TF gene. MSCs populations that obtained from umbilical cord were cultured and expanded in the appropriate medium cell culture. The identity of the MSCs was verified through flow cytometry, and their ability to differentiate into osteogenic and adipogenic lineages. Two gRNAs for Exons 1 and 2 of the TF gene have been designed and cloned into px458 vector's backbone (pSpCas9 (BB)-2A-GFP). Following transfecting of gRNAs into HUCMSCs and successfully knocking out the TF gene using GAP-PCR, the impact of normal and knockout HUCMSCs on coagulation was assessed through prothrombin time (PT), D-dimer level, clotting time (CT), and turbidity assay. Furthermore, the impact of TF knockout (TFKO) on MMP19 expression was assessed. Our results revealed that the PT was prolonged and D-dimer level was decreased in TFKO group compared to normal HUCMSCs. These findings suggest that TF gene plays a crucial role in regulating coagulation in HUCMSCs. Also, a significant reduction in MMP19 expression was observed within the TFKO group.

摘要

多能间充质基质/干细胞(MSCs)是指一群具有独特祖细胞特征的干细胞,包括分化为多种细胞类型的潜力。由于MSCs具有独特的特性,如能够分化为多种细胞类型、具有扩增能力、自我更新能力和免疫调节作用,它们已成为细胞治疗和组织再生的有希望的候选者。然而,在过去十年中,有报道关注到与MSCs治疗相关的血栓形成并发症。由于组织因子(TF)是MSCs表达的一种强大的凝血激活剂,可刺激外源性凝血途径,我们研究了敲除TF基因后人脐带间充质干细胞(HUCMSCs)的血栓形成特性。从脐带获得的MSCs群体在适当的细胞培养基中进行培养和扩增。通过流式细胞术验证MSCs的身份,以及它们分化为成骨和成脂谱系的能力。针对TF基因的外显子1和2设计了两种gRNA,并将其克隆到px458载体骨架(pSpCas9(BB)-2A-GFP)中。将gRNA转染到HUCMSCs中,并使用GAP-PCR成功敲除TF基因后,通过凝血酶原时间(PT)、D-二聚体水平、凝血时间(CT)和比浊法评估正常和敲除TF基因的HUCMSCs对凝血的影响。此外,评估了TF基因敲除(TFKO)对MMP19表达的影响。我们的结果显示,与正常HUCMSCs相比,TFKO组的PT延长,D-二聚体水平降低。这些发现表明TF基因在调节HUCMSCs的凝血中起关键作用。此外,在TFKO组中观察到MMP19表达显著降低。

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