Rong Yanyan, Lu Wei, Huang Xianbao, Ji Dexiang, Tang Dehong, Huang Ruibin, Zhou Wenhua, Chen Guoan, He Yue
Department of Hematology, First Affiliated Hospital of Nanchang University, Nanchang, 330000, Jiangxi, China.
Department of Blood Transfusion, First Affiliated Hospital of Gannan Medical College, Ganzhou, 341000, Jiangxi, China.
Hum Cell. 2024 Dec 19;38(1):31. doi: 10.1007/s13577-024-01162-y.
Immune thrombocytopenia (ITP) is a common hematological disorder. Our previous study has found that exosomal miR-146a-5p derived from bone marrow mesenchymal stromal cells (BMSCs) regulate Th17/Treg balance to alleviate ITP. This work further investigated the role of miR-146a-5p in ITP with pregnancy. Compared with healthy pregnant volunteers, the levels of Th1 cells and IFN-γ were increased, the levels of Th2 cells and IL-4 were decreased in peripheral blood of ITP patients with pregnancy. Then, human BMSCs-exosomes repressed the ratio of Th1/Th2 cells in CD4 T cells, while BMSCs-exosomes with miR-146a-5p inhibitor increased Th1/Th2 cell ratio. Moreover, an ITP mouse model with pregnancy was constructed by administering anti-CD41 antibody in pregnant mice to verify the role of BMSCs-Exo in vivo. BMSCs-Exo elevated the number of platelet and megakaryocyte, improved the function of gastric, spleen and thymus tissues in ITP mice with pregnancy, which attributed to delivery miR-146a-5p. Furthermore, miR-146a-5p interacted with CARD10, and then repressed CARD10/NF-κB signaling pathway. BMSCs-exosomes promoted proliferation and inhibited apoptosis of Dami cells. In conclusion, BMSCs-exosomal miR-146a-5p reduced Th1/Th2 cell ratio to elevate proliferation and inhibit apoptosis of Dami cells, thereby alleviating ITP with pregnancy development. Therefore, miR-146a-5p may be a target for ITP with pregnancy treatment.
免疫性血小板减少症(ITP)是一种常见的血液系统疾病。我们之前的研究发现,源自骨髓间充质基质细胞(BMSCs)的外泌体miR-146a-5p可调节Th17/Treg平衡以缓解ITP。这项工作进一步研究了miR-146a-5p在妊娠合并ITP中的作用。与健康妊娠志愿者相比,妊娠合并ITP患者外周血中Th1细胞和IFN-γ水平升高,Th2细胞和IL-4水平降低。然后,人BMSCs外泌体抑制CD4 T细胞中Th1/Th2细胞的比例,而携带miR-146a-5p抑制剂的BMSCs外泌体则增加Th1/Th2细胞比例。此外,通过给妊娠小鼠注射抗CD41抗体构建了妊娠合并ITP的小鼠模型,以验证BMSCs-Exo在体内的作用。BMSCs-Exo增加了妊娠合并ITP小鼠的血小板和巨核细胞数量,改善了胃、脾和胸腺组织的功能,这归因于其递送了miR-146a-5p。此外,miR-146a-5p与CARD10相互作用,进而抑制CARD10/NF-κB信号通路。BMSCs外泌体促进了Dami细胞的增殖并抑制其凋亡。总之,BMSCs外泌体miR-146a-5p降低了Th1/Th2细胞比例,以提高Dami细胞的增殖并抑制其凋亡,从而缓解妊娠合并ITP的病情发展。因此,miR-146a-5p可能是妊娠合并ITP治疗的一个靶点。