Department of Physiology and Cell Biology, College of Medicine, The Ohio State University, Columbus, Ohio.
Jackson Department of Veterans Affairs Medical Center, Jackson, Mississippi.
Am J Physiol Cell Physiol. 2022 Mar 1;322(3):C354-C369. doi: 10.1152/ajpcell.00411.2021. Epub 2022 Jan 19.
Suppressing mineralocorticoid receptor (MR) activity with MR antagonists is therapeutic for chronic skeletal muscle pathology in Duchenne muscular dystrophy (DMD) mouse models. Although mechanisms underlying clinical MR antagonist efficacy for DMD cardiomyopathy and other cardiac diseases are defined, mechanisms in skeletal muscles are not fully elucidated. Myofiber MR knockout improves skeletal muscle force and a subset of dystrophic pathology. However, MR signaling in myeloid cells is known to be a major contributor to cardiac efficacy. To define contributions of myeloid MR in skeletal muscle function and disease, we performed parallel assessments of muscle pathology, cytokine levels, and myeloid cell populations resulting from myeloid MR genetic knockout in muscular dystrophy and acute muscle injury. Myeloid MR knockout led to lower levels of C-C motif chemokine receptor 2 (CCR2)-expressing macrophages, resulting in sustained myofiber damage after acute injury of normal muscle. In acute injury, myeloid MR knockout also led to increased local muscle levels of the enzyme that produces the endogenous MR agonist aldosterone, further supporting important contributions of MR signaling in normal muscle repair. In muscular dystrophy, myeloid MR knockout altered cytokine levels differentially between quadriceps and diaphragm muscles, which contain different myeloid populations. Myeloid MR knockout led to higher levels of fibrosis in dystrophic diaphragm. These results support important contributions of myeloid MR signaling to skeletal muscle repair in acute and chronic injuries and highlight the useful information gained from cell-specific genetic knockouts to delineate mechanisms of pharmacological efficacy.
抑制盐皮质激素受体 (MR) 活性的 MR 拮抗剂在 Duchenne 肌营养不良症 (DMD) 小鼠模型的慢性骨骼肌病变的治疗中具有疗效。尽管已经确定了临床 MR 拮抗剂治疗 DMD 心肌病和其他心脏疾病的机制,但骨骼肌中的机制尚未完全阐明。肌纤维 MR 敲除可改善骨骼肌力量和一部分肌营养不良病理。然而,已知髓样细胞中的 MR 信号是心脏疗效的主要贡献者。为了确定髓样 MR 在骨骼肌功能和疾病中的作用,我们平行评估了肌肉病理学、细胞因子水平和髓样细胞群,这些结果是通过在肌营养不良症和急性肌肉损伤中进行髓样 MR 基因敲除而得到的。髓样 MR 敲除导致 C-C 基序趋化因子受体 2 (CCR2) 表达的巨噬细胞水平降低,导致正常肌肉急性损伤后肌纤维持续损伤。在急性损伤中,髓样 MR 敲除还导致产生内源性 MR 激动剂醛固酮的酶在局部肌肉水平升高,进一步支持 MR 信号在正常肌肉修复中的重要作用。在肌营养不良症中,髓样 MR 敲除改变了四头肌和膈肌之间的细胞因子水平,而这两块肌肉中含有不同的髓样细胞群。髓样 MR 敲除导致肌营养不良症的膈肌纤维化水平升高。这些结果支持髓样 MR 信号对急性和慢性损伤中骨骼肌修复的重要作用,并强调了从细胞特异性基因敲除中获得的有用信息,以阐明药物疗效的机制。