Usuelli Vera, Ben Nasr Moufida, D'Addio Francesca, Liu Kaifeng, Vergani Andrea, El Essawy Basset, Yang Jun, Assi Emma, Uehara Mayuko, Rossi Chiara, Solini Anna, Capobianco Annalisa, Rigamonti Elena, Potena Luciano, Venturini Massimo, Sabatino Mario, Bottarelli Lorena, Ammirati Enrico, Frigerio Maria, Castillo-Leon Eduardo, Maestroni Anna, Azzoni Cinzia, Loretelli Cristian, Joe Seelam Andy, Tai Albert K, Pastore Ida, Becchi Gabriella, Corradi Domenico, Visner Gary A, Zuccotti Gian V, Chau Nelson B, Abdi Reza, Pezzolesi Marcus G, Fiorina Paolo
International Center for T1D, Pediatric Clinical Research Center "Romeo ed Enrica Invernizzi", Department of Biomedical and Clinical Science L. Sacco, Universita Degli Studi di Milano, Milan, Italy.
Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Am J Transplant. 2021 Oct;21(10):3280-3295. doi: 10.1111/ajt.16581. Epub 2021 May 3.
Despite much progress in improving graft outcome during cardiac transplantation, chronic allograft vasculopathy (CAV) remains an impediment to long-term graft survival. MicroRNAs (miRNAs) emerged as regulators of the immune response. Here, we aimed to examine the miRNA network involved in CAV. miRNA profiling of heart samples obtained from a murine model of CAV and from cardiac-transplanted patients with CAV demonstrated that miR-21 was most significantly expressed and was primarily localized to macrophages. Interestingly, macrophage depletion with clodronate did not significantly prolong allograft survival in mice, while conditional deletion of miR-21 in macrophages or the use of a specific miR-21 antagomir resulted in indefinite cardiac allograft survival and abrogated CAV. The immunophenotype, secretome, ability to phagocytose, migration, and antigen presentation of macrophages were unaffected by miR-21 targeting, while macrophage metabolism was reprogrammed, with a shift toward oxidative phosphorylation in naïve macrophages and with an inhibition of glycolysis in pro-inflammatory macrophages. The aforementioned effects resulted in an increase in M2-like macrophages, which could be reverted by the addition of L-arginine. RNA-seq analysis confirmed alterations in arginase-associated pathways associated with miR-21 antagonism. In conclusion, miR-21 is overexpressed in murine and human CAV, and its targeting delays CAV onset by reprogramming macrophages metabolism.
尽管在改善心脏移植后的移植物预后方面取得了很大进展,但慢性移植物血管病(CAV)仍然是长期移植物存活的一个障碍。微小RNA(miRNA)作为免疫反应的调节因子出现。在此,我们旨在研究参与CAV的miRNA网络。对从CAV小鼠模型和患有CAV的心脏移植患者获得的心脏样本进行miRNA分析表明,miR-21表达最为显著,且主要定位于巨噬细胞。有趣的是,用氯膦酸盐清除巨噬细胞并未显著延长小鼠同种异体移植物的存活时间,而巨噬细胞中miR-21的条件性缺失或使用特异性miR-21拮抗剂则导致心脏同种异体移植物无限期存活并消除了CAV。巨噬细胞的免疫表型、分泌组、吞噬能力、迁移和抗原呈递不受miR-21靶向的影响,而巨噬细胞代谢被重新编程,幼稚巨噬细胞向氧化磷酸化转变,促炎巨噬细胞的糖酵解受到抑制。上述效应导致M2样巨噬细胞增加,添加L-精氨酸可使其逆转。RNA测序分析证实了与miR-21拮抗相关的精氨酸酶相关途径的改变。总之,miR-21在小鼠和人类CAV中过表达,其靶向通过重新编程巨噬细胞代谢延迟了CAV的发生。