Cimini Maria, Cannatá Antonio, Pasquinelli Gianandrea, Rota Marcello, Goichberg Polina
Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.
Unit of Surgical Pathology, Department of Experimental, Diagnostic and Specialty Medicine (DIMES), S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
PLoS One. 2017 Mar 23;12(3):e0173927. doi: 10.1371/journal.pone.0173927. eCollection 2017.
Cardiac lymphatic vasculature undergoes substantial expansion in response to myocardial infarction (MI). However, there is limited information on the cellular mechanisms mediating post-MI lymphangiogenesis and accompanying fibrosis in the infarcted adult heart. Using a mouse model of permanent coronary artery ligation, we examined spatiotemporal changes in the expression of lymphendothelial and mesenchymal markers in the acutely and chronically infarcted myocardium. We found that at the time of wound granulation, a three-fold increase in the frequency of podoplanin-labeled cells occurred in the infarcted hearts compared to non-operated and sham-operated counterparts. Podoplanin immunoreactivity detected LYVE-1-positive lymphatic vessels, as well as masses of LYVE-1-negative cells dispersed between myocytes, predominantly in the vicinity of the infarcted region. Podoplanin-carrying populations displayed a mesenchymal progenitor marker PDGFRα, and intermittently expressed Prox-1, a master regulator of the lymphatic endothelial fate. At the stages of scar formation and maturation, concomitantly with the enlargement of lymphatic network in the injured myocardium, the podoplanin-rich LYVE-1-negative multicellular assemblies were apparent in the fibrotic area, aligned with extracellular matrix deposits, or located in immediate proximity to activated blood vessels with high VEGFR-2 content. Of note, these podoplanin-containing cells acquired the expression of PDGFRβ or a hematoendothelial epitope CD34. Although Prox-1 labeling was abundant in the area affected by MI, the podoplanin-presenting cells were not consistently Prox-1-positive. The concordance of podoplanin with VEGFR-3 similarly varied. Thus, our data reveal previously unknown phenotypic and structural heterogeneity within the podoplanin-positive cell compartment in the infarcted heart, and suggest an alternate ability of podoplanin-presenting cardiac cells to generate lymphatic endothelium and pro-fibrotic cells, contributing to scar development.
心肌梗死后,心脏淋巴管系统会发生显著扩张。然而,关于介导梗死成年心脏心肌梗死后淋巴管生成及伴随纤维化的细胞机制,相关信息有限。利用永久性冠状动脉结扎的小鼠模型,我们研究了急性和慢性梗死心肌中淋巴管内皮标志物和间充质标志物表达的时空变化。我们发现,在伤口肉芽形成期,梗死心脏中血小板内皮细胞黏附分子标记细胞的频率相较于未手术和假手术的对照组增加了两倍。血小板内皮细胞黏附分子免疫反应检测到淋巴管内皮细胞受体-1阳性淋巴管,以及分散在心肌细胞之间的淋巴管内皮细胞受体-1阴性细胞团,主要位于梗死区域附近。携带血小板内皮细胞黏附分子的细胞群体表现出间充质祖细胞标志物血小板衍生生长因子受体α,并间歇性表达Prox-1,后者是淋巴管内皮命运的主要调节因子。在瘢痕形成和成熟阶段,随着损伤心肌中淋巴管网的扩大,富含血小板内皮细胞黏附分子的淋巴管内皮细胞受体-1阴性多细胞集合体在纤维化区域明显可见,与细胞外基质沉积物对齐,或紧邻血管内皮生长因子受体-2含量高的活化血管。值得注意的是,这些含血小板内皮细胞黏附分子的细胞获得了血小板衍生生长因子受体β或造血内皮表位CD34的表达。尽管Prox-1标记在心肌梗死影响的区域丰富,但呈现血小板内皮细胞黏附分子的细胞并非始终为Prox-1阳性。血小板内皮细胞黏附分子与血管内皮生长因子受体-3的一致性同样存在差异。因此,我们的数据揭示了梗死心脏中血小板内皮细胞黏附分子阳性细胞区室内先前未知的表型和结构异质性,并表明呈现血小板内皮细胞黏附分子的心脏细胞具有生成淋巴管内皮细胞和促纤维化细胞的替代能力,有助于瘢痕形成。