Immune profiling of murine cardiac leukocytes identifies triggering receptor expressed on myeloid cells 2 as a novel mediator of hypertensive heart failure

被引:14
作者
Smart, Charles Duncan [1 ]
Fehrenbach, Daniel J. [2 ]
Wassenaar, Jean W. [3 ]
Agrawal, Vineet [3 ]
Fortune, Niki L. [4 ]
Dixon, Debra D. [3 ]
Cottam, Matthew A. [1 ]
Hasty, Alyssa H. [1 ,4 ]
Hemnes, Anna R. [5 ]
Doran, Amanda C. [3 ,6 ]
Gupta, Deepak K. [3 ,7 ]
Madhur, Meena S. [1 ,2 ,3 ,6 ]
机构
[1] Vanderbilt Univ, Dept Mol Physiol & Biophys, 2201 West End Ave, Nashville, TN 37235 USA
[2] Vanderbilt Univ Med Ctr VUMC, Dept Med, Div Clin Pharmacol, 2215 Garland Ave, P415D MRB 4, Nashville, TN 37232 USA
[3] Vanderbilt Univ Med Ctr VUMC, Dept Med, Div Cardiovasc Med, 1311 Med Ctr Dr, Nashville, TN 37232 USA
[4] VA Tennessee Valley Healthcare Syst, Nashville, TN 37212 USA
[5] Vanderbilt Univ Med Ctr VUMC, Dept Med, Div Allergy Pulm & Crit Care, Nashville, TN USA
[6] Vanderbilt Univ Med Ctr VUMC, Vanderbilt Inst Infect Immunol & Inflammat, Med Ctr North A-5121,1161 21st Ave South, Nashville, TN 37232 USA
[7] Vanderbilt Univ, Vanderbilt Translat & Clin Cardiovasc Res Ctr, Med Ctr, Nashville, TN USA
关键词
Hypertension; Heart failure; TREM2; Macrophage; Inflammation; II-INDUCED HYPERTENSION; DIASTOLIC DYSFUNCTION; MYOCARDIAL FIBROSIS; TYROSINE KINASE; BLOOD-PRESSURE; MACROPHAGES; INFLAMMATION; DISTINCT; MODEL; MICROGLIA;
D O I
10.1093/cvr/cvad093
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Heart failure with preserved ejection fraction (HFpEF) is characterized by diastolic dysfunction, microvascular dysfunction, and myocardial fibrosis with recent evidence implicating the immune system in orchestrating cardiac remodelling. Methods and results Here, we show the mouse model of deoxycorticosterone acetate (DOCA)-salt hypertension induces key elements of HFpEF, including diastolic dysfunction, exercise intolerance, and pulmonary congestion in the setting of preserved ejection fraction. A modified single-cell sequencing approach, cellular indexing of transcriptomes and epitopes by sequencing, of cardiac immune cells reveals an altered abundance and transcriptional signature in multiple cell types, most notably cardiac macrophages. The DOCA-salt model results in differential expression of several known and novel genes in cardiac macrophages, including up-regulation of Trem2, which has been recently implicated in obesity and atherosclerosis. The role of Trem2 in hypertensive heart failure, however, is unknown. We found that mice with genetic deletion of Trem2 exhibit increased cardiac hypertrophy, diastolic dysfunction, renal injury, and decreased cardiac capillary density after DOCA-salt treatment compared to wild-type controls. Moreover, Trem2-deficient macrophages have impaired expression of pro-angiogenic gene programmes and increased expression of pro-inflammatory cytokines. Furthermore, we found that plasma levels of soluble TREM2 are elevated in DOCA-salt treated mice and humans with heart failure. Conclusions Together, our data provide an atlas of immunological alterations that can lead to improved diagnostic and therapeutic strategies for HFpEF. We provide our dataset in an easy to explore and freely accessible web application making it a useful resource for the community. Finally, our results suggest a novel cardioprotective role for Trem2 in hypertensive heart failure.
引用
收藏
页码:2312 / 2328
页数:17
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