Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model

Abstract Glutaraldehyde‐fixed porcine heart valve (GPHV) calcify and deteriorate over time. The aim of this study was to explore the roles macrophages play in mediating calcification and degeneration of the valve's connective tissue matrix. GPHV were implanted subcutaneously in the abdomens of...

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Main Authors: Zongtao Liu, Yixuan Wang, Fei Xie, Xing Liu, Fei Li, Nianguo Dong
Format: Article
Language:English
Published: Wiley 2021-02-01
Series:Pharmacology Research & Perspectives
Subjects:
Online Access:https://doi.org/10.1002/prp2.716
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spelling doaj-bd1b7708eea6445a866984b5eb5a842d2021-05-03T00:22:04ZengWileyPharmacology Research & Perspectives2052-17072021-02-0191n/an/a10.1002/prp2.716Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal modelZongtao Liu0Yixuan Wang1Fei Xie2Xing Liu3Fei Li4Nianguo Dong5Department of Cardiovascular Surgery Union HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan ChinaDepartment of Cardiovascular Surgery Union HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan ChinaDepartment of Cardiovascular Surgery Union HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan ChinaDepartment of Cardiovascular Surgery Union HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan ChinaDepartment of Cardiovascular Surgery Union HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan ChinaDepartment of Cardiovascular Surgery Union HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan ChinaAbstract Glutaraldehyde‐fixed porcine heart valve (GPHV) calcify and deteriorate over time. The aim of this study was to explore the roles macrophages play in mediating calcification and degeneration of the valve's connective tissue matrix. GPHV were implanted subcutaneously in the abdomens of C57BL/6 mice. The mice were equally divided into two study groups: (a) GPHV +phosphate buffered saline (PBS) liposomes, and (b) GPHV +clodronate liposomes. GPHV were collected for further analyses at 4 weeks post implant. Macrophages were almost depleted from the spleens of mice injected with clodronate liposomes as indicated by immunohistochemical staining. Furthermore, the expression of matrix metalloproteinase‐2 (MMP‐2), MMP‐9, and proinflammatory cytokines like IL‐1β, IL‐6, MCP‐1, MIP‐1a, MIP‐1b, were downregulated in the GPHV +Clodronate liposomal group compared with the GPHV+PBS liposomal group. Clodronate liposomal treatment led to significant decreases in the expression of RUNX2, ALP and OPN as well as less calcium deposits in GPHVs compared with PBS liposomal treatment. This finding indicated that infiltrating macrophages are critically involved in the development of calcification and deterioration in GPHVs. Macrophage depletion by clodronate liposomes decreased the extent of GPHV’s calcification and deterioration.https://doi.org/10.1002/prp2.716Clodronate liposomesGlutaraldehyde‐fixed porcine heart valvemacrophagemetalloproteinasestructural valve degeneration
collection DOAJ
language English
format Article
sources DOAJ
author Zongtao Liu
Yixuan Wang
Fei Xie
Xing Liu
Fei Li
Nianguo Dong
spellingShingle Zongtao Liu
Yixuan Wang
Fei Xie
Xing Liu
Fei Li
Nianguo Dong
Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model
Pharmacology Research & Perspectives
Clodronate liposomes
Glutaraldehyde‐fixed porcine heart valve
macrophage
metalloproteinase
structural valve degeneration
author_facet Zongtao Liu
Yixuan Wang
Fei Xie
Xing Liu
Fei Li
Nianguo Dong
author_sort Zongtao Liu
title Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model
title_short Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model
title_full Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model
title_fullStr Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model
title_full_unstemmed Elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model
title_sort elimination of macrophages reduces glutaraldehyde‐fixed porcine heart valve degeneration in mice subdermal model
publisher Wiley
series Pharmacology Research & Perspectives
issn 2052-1707
publishDate 2021-02-01
description Abstract Glutaraldehyde‐fixed porcine heart valve (GPHV) calcify and deteriorate over time. The aim of this study was to explore the roles macrophages play in mediating calcification and degeneration of the valve's connective tissue matrix. GPHV were implanted subcutaneously in the abdomens of C57BL/6 mice. The mice were equally divided into two study groups: (a) GPHV +phosphate buffered saline (PBS) liposomes, and (b) GPHV +clodronate liposomes. GPHV were collected for further analyses at 4 weeks post implant. Macrophages were almost depleted from the spleens of mice injected with clodronate liposomes as indicated by immunohistochemical staining. Furthermore, the expression of matrix metalloproteinase‐2 (MMP‐2), MMP‐9, and proinflammatory cytokines like IL‐1β, IL‐6, MCP‐1, MIP‐1a, MIP‐1b, were downregulated in the GPHV +Clodronate liposomal group compared with the GPHV+PBS liposomal group. Clodronate liposomal treatment led to significant decreases in the expression of RUNX2, ALP and OPN as well as less calcium deposits in GPHVs compared with PBS liposomal treatment. This finding indicated that infiltrating macrophages are critically involved in the development of calcification and deterioration in GPHVs. Macrophage depletion by clodronate liposomes decreased the extent of GPHV’s calcification and deterioration.
topic Clodronate liposomes
Glutaraldehyde‐fixed porcine heart valve
macrophage
metalloproteinase
structural valve degeneration
url https://doi.org/10.1002/prp2.716
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