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消除巨噬细胞可减少皮下植入猪心瓣膜的戊二醛固定后在小鼠体内的退行性变。

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

机构信息

Department of Cardiovascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Pharmacol Res Perspect. 2021 Feb;9(1):e00716. doi: 10.1002/prp2.716.

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.

摘要

戊二醛固定猪心瓣(GPHV)会随着时间的推移而钙化和恶化。本研究旨在探讨巨噬细胞在介导瓣膜结缔组织基质钙化和退变中的作用。将 GPHV 皮下植入 C57BL/6 小鼠的腹部。将小鼠等分为两组进行研究:(a)GPHV+磷酸盐缓冲盐水(PBS)脂质体,和(b)GPHV+氯膦酸脂质体。在植入后 4 周收集 GPHV 进行进一步分析。免疫组织化学染色表明,注射氯膦酸脂质体的小鼠脾脏中的巨噬细胞几乎被耗尽。此外,与 GPHV+PBS 脂质体组相比,GPHV+Clodronate 脂质体组中基质金属蛋白酶-2(MMP-2)、MMP-9 和促炎细胞因子如 IL-1β、IL-6、MCP-1、MIP-1a、MIP-1b 的表达下调。氯膦酸脂质体治疗导致 GPHV 中 RUNX2、ALP 和 OPN 的表达显著降低,以及钙沉积减少,与 PBS 脂质体治疗相比。这一发现表明,浸润的巨噬细胞在 GPHV 钙化和恶化的发展中起着至关重要的作用。氯膦酸脂质体耗尽巨噬细胞可减少 GPHV 钙化和恶化的程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365e/7849454/756315d5837d/PRP2-9-e00716-g001.jpg

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