Intravenous injection of PCSK9 gain-of-function mutation in C57BL/6J background mice on Angiotensin II-induced AAA

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xingli Xu , Xiaohui Li , Chungang Zhai , Yuxin Yao , Xiang Li , Chunjie Ming , Juanjuan Sun , Hao Wang , Yang Mao , Lei Zhang
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引用次数: 0

Abstract

Objective

This study was performed to compare the incidence of Angiotensin II (Ang II)-induced abdominal aortic aneurysms (AAA) between intravenous and intraperitoneal injection of AAV8.mPCSK9D377Y in wild-type (WT) mice with C57BL/6J background and the pathological differences of above model in WT and ApoE−/− mice.

Design

Male WT mice were injected intraperitoneally or intravenously with either a AAV8.null or AAV8.mPCSK9D377Y. Two weeks after injection, all WT mice were infused with Ang II, and simultaneously age-matched male ApoE−/− mice were infused with saline or Ang II for 4 weeks.

Results

Compared with intraperitoneal injection of AAV8.mPCSK9D377Y for AAA model in WT mice, a higher incidence of Ang II-induced AAA, increased blood pressure (BP) and lipid concentration, lower collagen deposition and up-regulated inflammation response were shown by intravenous injection, which was similar to ApoE−/− mice infused with Ang II.

Conclusion

AAV8.mPCSK9D377Y infected male WT mice intravenously facilitate a high incident and comparable severity of Ang II-induced AAA which could be greatly expedites AAA studies on a gene of interest.
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来源期刊
CiteScore
12.30
自引率
0.00%
发文量
218
审稿时长
32 days
期刊介绍: BBA Molecular Basis of Disease addresses the biochemistry and molecular genetics of disease processes and models of human disease. This journal covers aspects of aging, cancer, metabolic-, neurological-, and immunological-based disease. Manuscripts focused on using animal models to elucidate biochemical and mechanistic insight in each of these conditions, are particularly encouraged. Manuscripts should emphasize the underlying mechanisms of disease pathways and provide novel contributions to the understanding and/or treatment of these disorders. Highly descriptive and method development submissions may be declined without full review. The submission of uninvited reviews to BBA - Molecular Basis of Disease is strongly discouraged, and any such uninvited review should be accompanied by a coverletter outlining the compelling reasons why the review should be considered.
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