Literature DB >> 28431249

Macrophages Facilitate Electrical Conduction in the Heart.

Maarten Hulsmans1, Sebastian Clauss2, Ling Xiao3, Aaron D Aguirre4, Kevin R King1, Alan Hanley5, William J Hucker3, Eike M Wülfers6, Gunnar Seemann6, Gabriel Courties1, Yoshiko Iwamoto1, Yuan Sun1, Andrej J Savol7, Hendrik B Sager1, Kory J Lavine8, Gregory A Fishbein9, Diane E Capen1, Nicolas Da Silva1, Lucile Miquerol10, Hiroko Wakimoto11, Christine E Seidman12, Jonathan G Seidman11, Ruslan I Sadreyev13, Kamila Naxerova11, Richard N Mitchell9, Dennis Brown1, Peter Libby14, Ralph Weissleder15, Filip K Swirski1, Peter Kohl16, Claudio Vinegoni1, David J Milan17, Patrick T Ellinor17, Matthias Nahrendorf18.   

Abstract

Organ-specific functions of tissue-resident macrophages in the steady-state heart are unknown. Here, we show that cardiac macrophages facilitate electrical conduction through the distal atrioventricular node, where conducting cells densely intersperse with elongated macrophages expressing connexin 43. When coupled to spontaneously beating cardiomyocytes via connexin-43-containing gap junctions, cardiac macrophages have a negative resting membrane potential and depolarize in synchrony with cardiomyocytes. Conversely, macrophages render the resting membrane potential of cardiomyocytes more positive and, according to computational modeling, accelerate their repolarization. Photostimulation of channelrhodopsin-2-expressing macrophages improves atrioventricular conduction, whereas conditional deletion of connexin 43 in macrophages and congenital lack of macrophages delay atrioventricular conduction. In the Cd11bDTR mouse, macrophage ablation induces progressive atrioventricular block. These observations implicate macrophages in normal and aberrant cardiac conduction.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  atrioventricular node; computational modeling; connexin 43; electrical conduction; gap junctions; heart; macrophages; optogenetics; single-cell RNA-sequencing; tissue clearing

Mesh:

Substances:

Year:  2017        PMID: 28431249      PMCID: PMC5474950          DOI: 10.1016/j.cell.2017.03.050

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  51 in total

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Authors:  Y Shibata; T Yamamoto
Journal:  Cell Tissue Res       Date:  1977-03-24       Impact factor: 5.249

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Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-13       Impact factor: 11.205

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Authors:  Ernesto Oviedo-Orta; W Howard Evans
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