Yang Fanmuyi, Dong Anping, Ahamed Jasimuddin, Sunkara Manjula, Smyth Susan S
Division of Cardiovascular Medicine, Gill Heart Institute, University of Kentucky, Lexington, Kentucky;
Laboratory of Blood and Vascular Biology, Rockefeller University, New York, New York; and.
Am J Physiol Heart Circ Physiol. 2014 Nov 15;307(10):H1529-38. doi: 10.1152/ajpheart.00951.2013. Epub 2014 Sep 19.
Bone marrow-derived inflammatory cells, including platelets, may contribute to the progression of pressure overload-induced left ventricular hypertrophy (LVH). However, the underlying mechanisms for this are still unclear. One potential mechanism is through release of granule cargo. Unc13-d(Jinx) (Jinx) mice, which lack Munc13-4, a limiting factor in vesicular priming and fusion, have granule secretion defects in a variety of hematopoietic cells, including platelets. In the current study, we investigated the role of granule secretion in the development of LVH and cardiac remodeling using chimeric mice specifically lacking Munc13-4 in marrow-derived cells. Pressure overload was elicited by transverse aortic constriction (TAC). Chimeric mice were created by bone marrow transplantation. Echocardiography, histology staining, immunohistochemistry, real-time polymerase chain reaction, enzyme-linked immunosorbent assay, and mass spectrometry were used to study LVH progression and inflammatory responses. Wild-type (WT) mice that were transplanted with WT bone marrow (WT→WT) and WT mice that received Jinx bone marrow (Jinx→WT) developed LVH and a classic fetal reprogramming response early (7 days) after TAC. However, at late times (5 wk), mice lacking Munc13-4 in bone marrow-derived cells (Jinx→WT) failed to sustain the cardiac hypertrophy observed in WT chimeric mice. No difference in cardiac fibrosis was observed at early or late time points. Reinjection of WT platelets or platelet releasate partially restored cardiac hypertrophy in Jinx chimeric mice. These results suggest that sustained LVH in the setting of pressure overload depends on one or more factors secreted from bone marrow-derived cells, possibly from platelets. Inhibiting granule cargo release may represent a novel target for preventing sustained LVH.
包括血小板在内的骨髓源性炎症细胞可能会促使压力负荷诱导的左心室肥厚(LVH)进展。然而,其潜在机制仍不清楚。一种潜在机制是通过颗粒内容物的释放。Unc13-d(Jinx)(Jinx)小鼠缺乏Munc13-4,而Munc13-4是囊泡启动和融合的限制因素,在包括血小板在内的多种造血细胞中存在颗粒分泌缺陷。在本研究中,我们使用骨髓源性细胞中特异性缺乏Munc13-4的嵌合小鼠,研究颗粒分泌在LVH发展和心脏重塑中的作用。通过横向主动脉缩窄(TAC)引发压力负荷。通过骨髓移植创建嵌合小鼠。使用超声心动图、组织学染色、免疫组织化学、实时聚合酶链反应、酶联免疫吸附测定和质谱来研究LVH进展和炎症反应。移植野生型(WT)骨髓的WT小鼠(WT→WT)和接受Jinx骨髓的WT小鼠(Jinx→WT)在TAC后早期(7天)出现LVH和典型的胎儿重编程反应。然而,在晚期(5周),骨髓源性细胞中缺乏Munc13-4的小鼠(Jinx→WT)未能维持WT嵌合小鼠中观察到的心脏肥大。在早期或晚期时间点均未观察到心脏纤维化的差异。再次注射WT血小板或血小板释放物可部分恢复Jinx嵌合小鼠的心脏肥大。这些结果表明,在压力负荷情况下持续的LVH取决于骨髓源性细胞分泌的一种或多种因子,可能来自血小板。抑制颗粒内容物释放可能是预防持续性LVH的新靶点。