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Angiogenic Role of LYVE-1–Positive Macrophages in Adipose Tissue
Open accessAbstract
Here we report the discovery of a characteristic dense vascular network (DVN) in the tip portion of epididymal adipose tissue in adult mice. The DVN is formed by angiogenesis rather than by vasculogenesis, and has functional blood circulation. This DVN and its subsequent branching may provide a new functional route for adipogenesis. The recruitment, infiltration, and accumulation of bone marrow-derived LYVE-1 + macrophages in the tip region are crucial for the formation of the DVN. Matrix metalloproteinases (MMPs) and the VEGF-VEGFR2 system are responsible not only for the formation of the DVN, but also for the recruitment and infiltration of LYVE-1 + macrophages into the epididymal adipose tissue tip region. SDF-1, but not the MCP-1-CCR2 system, is a critical factor in recruitment and ongoing retention of macrophages in this area. We also demonstrate that the tip region of epididymal adipose tissue is highly hypoxic, and thus provides a microenvironment conducive to the high expression and enhanced activities of VEGF, VEGFR2, MMPs, and SDF-1 in autocrine and paracrine manners, to create an ideal niche for the recruitment, retention, and angiogenic action of macrophages. These findings shed light on the complex interplay between macrophage infiltration, angiogenesis, and adipogenesis in the tip region of adult epididymal adipose tissue, and provide novel insight into the regulation of alternative outgrowth of adipose tissue.
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“The hypoxic regions at the tip of the mouse epididymal fat pad have been shown to promote infiltration of a specific species of macrophage expressing the lymphatic endothelial marker LYVE-1.”
From The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis. (2017) · cites this paper as [52]
In the citing paper
“This new vasculature provides the framework for adipogenesis and growth of the fat pad (52).”
From The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis. (2017) · cites this paper as [52]
In the citing paper
“These LYVE-1 + macrophages promote angiogenesis through secretion of MMP-9, -12, and -7 to remodel the ECM and angiogenic factors like VEGF to stimulate the growth of a dense vascular network.”
From The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis. (2017) · cites this paper as [52]
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Nasim, S., Bichsel, C. A., Dayneka, S., Mannix, R. J., Holm, A., Vivero, M. P., Alexandrescu, S., Pinto, A., Greene, A. K., Ingber, D. E., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26698103
Nasim, S., Bichsel, C. A., Dayneka, S., Mannix, R. J., Holm, A., Vivero, M. P., Alexandrescu, S., Pinto, A., Greene, A. K., Ingber, D. E., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26698106
Nasim, S., Bichsel, C. A., Dayneka, S., Mannix, R. J., Holm, A., Vivero, M. P., Alexandrescu, S., Pinto, A., Greene, A. K., Ingber, D. E., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26698118
Nasim, S., Bichsel, C. A., Dayneka, S., Mannix, R. J., Holm, A., Vivero, M. P., Alexandrescu, S., Pinto, A., Greene, A. K., Ingber, D. E., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26698112
Nasim, S., Bichsel, C. A., Dayneka, S., Mannix, R. J., Holm, A., Vivero, M. P., Alexandrescu, S., Pinto, A., Greene, A. K., Ingber, D. E., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26698109
Additional file 1 of Endothelial-specific depletion of TGF-β signaling affects lymphatic function
Fukasawa, K., Hanada, K., Ichikawa, K., Hirashima, M., Takagi, T., Itoh, S., Watabe, T., & Itoh, F. (2021) · Figshare · doi:10.6084/m9.figshare.17104018
Metadata
- Authors
- Cho, C.-H., Jun Koh, Y., Han, J., Sung, H.-K., Jong Lee, H., Morisada, T., Schwendener, R. A., Brekken, R. A., Kang, G., Oike, Y., Choi, T.-S., Suda, T., Yoo, O.-J., & Koh, G. Y.
- Affiliations
- Korea Advanced Institute of Science and Technology (KR)
- From the National Research Laboratory of Vascular Biology and Department of Biological Sciences (C-H.C., Y.J.K., J.H., H-K. S., H.J.L., O-J.Y., G.Y.K.), Korea Advanced Institute of Science and Technology, Daejeon, Korea; Department of Cell Differentiation (T.M.,Y.O., T.S.), The Sakaguchi Laboratory, Keio University Internal Medicine, Tokyo, Japan; Laboratory of Liposome Research (R.A.S.), Institute of Molecular Cancer Research, University of Zurich, Switzerland; Departments of Surgery and...
- ORCID
- Venue
- Circulation Research
- Published
- 2007-03-02
- Volume
- 100
- Issue
- 4
- Pages
- e47-57
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W2150586369
- Cited by
- 309
- References
- 64
- Citations by year
- 2026: 8 · 2025: 14 · 2024: 30 · 2023: 13 · 2022: 19 · 2021: 19 · 2020: 13 · 2019: 12 · 2018: 19 · 2017: 7 · 2016: 12 · 2015: 10 · 2014: 14 · 2013: 27 · 2012: 14
- FWCI
- 7.81
- Type
- journal article
- Language
- en
- Open access
- green
- www.zora.uzh.ch
- Licence
- other-oa
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (acceptedVersion, other-oa)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion, other-oa)
- Zurich Open Repository and Archive (University of Zurich)
- Funders
- Korea Advanced Institute of Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Keywords
- adipose tissue angiogenesis, epididymal adipose tissue, adipogenesis, macrophage recruitment, CXCL12, VEGF/VEGFR2 signaling, matrix metalloproteinases, hypoxia, bone marrow-derived macrophages
- MeSH terms
- Adipose Tissue, Animals, Cell Movement, Epididymis, Glycoproteins, Macrophages, Male, Mice, Inbred C57BL, Mice, Knockout, Gene Expression Regulation, Developmental, Neovascularization, Physiologic, Membrane Transport Proteins, Adipogenesis, Mice
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