Capillary pruning couples tissue perfusion and oxygenation with cardiomyocyte maturation in the postnatal mouse heart

Front Cell Dev Biol. 2023 Nov 7:11:1256127. doi: 10.3389/fcell.2023.1256127. eCollection 2023.

Abstract

Introduction: Removal of poorly perfused capillaries by pruning contributes to remodeling the microvasculature to optimize oxygen and nutrient delivery. Blood flow drives this process by promoting the intravascular migration of endothelial cells in developing networks, such as in the yolk sac, zebrafish brain or postnatal mouse retina. Methods: In this study, we have implemented innovative tools to recognize capillary pruning in the complex 3D coronary microvasculature of the postnatal mouse heart. We have also experimentally tested the impact of decreasing pruning on the structure and function of this network by altering blood flow with two different vasodilators: losartan and prazosin. Results: Although both drugs reduced capillary pruning, a combination of experiments based on ex vivo imaging, proteomics, electron microscopy and in vivo functional approaches showed that losartan treatment resulted in an inefficient coronary network, reduced myocardial oxygenation and metabolic changes that delayed the arrest of cardiomyocyte proliferation, in contrast to the effects of prazosin, probably due to its concomitant promotion of capillary expansion. Discussion: Our work demonstrates that capillary pruning contributes to proper maturation and function of the heart and that manipulation of blood flow may be a novel strategy to refine the microvasculature and improve tissue perfusion after damage.

Keywords: blood flow; capillary pruning; cardiomyocyte maturation; metabolism; oxygenation; postnatal heart; vasodilators.

Grants and funding

The authors declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by grants SAF 2017-83229-R funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe” and PID 2020-112981RB-I00 funded by MCIN/AEI/10.13039/501100011033 (to AA), Deutsche Forschungsgemeinschaft grant HU 1294/8-1 (to AH) and PGC 2018-097019-B-I00, PID 2021-122348NB-I00, PLEC 2022-009235 and PLEC 2022-009298 from MCIN, P2022/BMD-7333l from CAM and HR17-00247 and HR22-00253 from “La Caixa” Banking Foundation (to JV). RS was a fellow of the FPI Severo Ochoa program CNIC (BES-2016-076636) funded by MCIN/AEI/10.13039/501100011033 and JC-C is a FPI fellow (PRE 2021-099875) funded by MCIN/AEI/10.13039/501100011033 and by “ESF Investing in your future”. CNIC is supported by the MCIN and the Pro CNIC Foundation, and is a Severo Ochoa Center of Excellence (CEX 2020‐001041‐S) funded by MCIN/AEI/10.13039/501100011033.