C3G通过增强巨核细胞生态位功能促进骨髓消融后骨髓脂肪细胞扩增和造血再生

IF 29.5 1区 医学 Q1 HEMATOLOGY
Óscar Herranz, Pablo Berrocal, Carmen Sicilia-Navarro, Cristina Fernández-Infante, Luis Hernández-Cano, Almudena Porras, Carmen Guerrero
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引用次数: 0

摘要

C3G是一种Rap1 GEF,促进巨核生成和血小板功能。利用巨核细胞靶向C3G的转基因和敲除小鼠模型,我们研究了C3G在5-氟尿嘧啶(5-FU)或全身照射(TBI)后骨髓移植后骨髓(BM)恢复期间是否也会影响巨核细胞的生态位功能。C3G促进恢复期巨核细胞成熟和血小板生成,同时增加白细胞和红细胞计数,提高5-FU重复剂量后雌性小鼠的存活率。此外,巨核细胞通过c3g介导的机制支持脂肪细胞分化,可能涉及Fgf1。BM巨核细胞和脂肪细胞数量或行为的变化影响造血干细胞库,在5-FU和tbi消融模型中,C3G促进其向髓-巨核细胞谱系倾斜。因此,C3G可能是化疗和/或骨髓移植患者造血功能增强治疗的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C3G promotes bone marrow adipocyte expansion and hematopoietic regeneration after myeloablation by enhancing megakaryocyte niche function
C3G, a Rap1 GEF, promotes megakaryopoiesis and platelet function. Using transgenic and knock-out mouse models targeting C3G in megakaryocytes, we investigated whether C3G also affects the niche function of megakaryocytes during bone marrow (BM) recovery after myeloablation induced by 5-fluorouracil (5-FU), or total body irradiation (TBI) followed by bone marrow transplantation. C3G promoted megakaryocyte maturation and platelet production during recovery, along with increased white and red blood cell counts and enhanced survival of female mice after repeated doses of 5-FU. Additionally, megakaryocytes favored adipocyte differentiation through a C3G-mediated mechanism, likely involving Fgf1. Changes in the number or behavior of BM megakaryocytes and adipocytes influenced the hematopoietic stem cell pool, with C3G promoting its bias towards the myeloid-megakaryocytic lineage in both 5-FU- and TBI-ablated models. Therefore, C3G could be a potential target in therapies aimed at enhancing hematopoiesis in patients undergoing chemotherapy and/or BM transplantation.
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来源期刊
CiteScore
48.10
自引率
2.10%
发文量
169
审稿时长
6-12 weeks
期刊介绍: The Journal of Hematology & Oncology, an open-access journal, publishes high-quality research covering all aspects of hematology and oncology, including reviews and research highlights on "hot topics" by leading experts. Given the close relationship and rapid evolution of hematology and oncology, the journal aims to meet the demand for a dedicated platform for publishing discoveries from both fields. It serves as an international platform for sharing laboratory and clinical findings among laboratory scientists, physician scientists, hematologists, and oncologists in an open-access format. With a rapid turnaround time from submission to publication, the journal facilitates real-time sharing of knowledge and new successes.
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