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MicroRNA-135a-3p regulates angiogenesis and tissue repair by targeting p38 signaling in endothelial cells
Basak Icli1, Winona Wu1, Denizhan Ozdemir1,2
1Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Abstract:
Angiogenesis is a critical process in repair of tissue injury that is regulated by a delicate balance between pro- and antiangiogenic factors. In disease states associated with impaired angiogenesis, we identified that miR-135a-3p is rapidly induced and serves as an antiangiogenic microRNA (miRNA) by targeting endothelial cell (EC) p38 signaling in vitro and in vivo. MiR-135a-3p overexpression significantly inhibited EC proliferation, migration, and network tube formation in matrigel, whereas miR-135-3p neutralization had the opposite effects. Mechanistic studies using transcriptomic profiling, bioinformatics, 3'-UTR reporter and miRNA ribonucleoprotein complex -immunoprecipitation assays, and small interfering RNA dependency studies revealed that miR-135a-3p inhibits the p38 signaling pathway in ECs by targeting huntingtin-interacting protein 1 (HIP1). Local delivery of miR-135a-3p inhibitors to wounds of diabetic db/db mice markedly increased angiogenesis, granulation tissue thickness, and wound closure rates, whereas local delivery of miR-135a-3p mimics impaired these effects. Finally, through gain- and loss-of-function studies in human skin organoids as a model of tissue injury, we demonstrated that miR-135a-3p potently modulated p38 signaling and angiogenesis in response to VEGF stimulation by targeting HIP1. These findings establish miR-135a-3p as a pivotal regulator of pathophysiological angiogenesis and tissue repair by targeting a VEGF-HIP1-p38K signaling axis, providing new targets for angiogenic therapy to promote tissue repair.-Icli, B., Wu, W., Ozdemir, D., Li, H., Haemmig, S., Liu, X., Giatsidis, G., Cheng, H. S., Avci, S. N., Kurt, M., Lee, N., Guimaraes, R. B., Manica, A., Marchini, J. F., Rynning, S. E., Risnes, I., Hollan, I., Croce, K., Orgill, D. P., Feinberg, M. W. MicroRNA-135a-3p regulates angiogenesis and tissue repair by targeting p38 signaling in endothelial cells.
Insights
MicroRNA-135a-3p acts as an antiangiogenic factor by inhibiting endothelial cell p38 signaling via HIP1. This microRNA (miRNA) is a key regulator of tissue repair and angiogenesis, offering new therapeutic targets.
Area of Science:
- Molecular Biology
- Cell Biology
- Regenerative Medicine
Background:
- Angiogenesis is crucial for tissue repair, requiring a balance of pro- and antiangiogenic factors.
- Impaired angiogenesis is linked to various disease states.
- MicroRNAs (miRNAs) are key regulators of cellular processes, including angiogenesis.
Purpose of the Study:
- To investigate the role of miR-135a-3p in angiogenesis and tissue repair.
- To identify the molecular targets and signaling pathways regulated by miR-135a-3p in endothelial cells.
- To evaluate the therapeutic potential of modulating miR-135a-3p for promoting tissue repair.
Main Methods:
- In vitro and in vivo studies using endothelial cells (ECs) and diabetic mouse wound models.
- Transcriptomic profiling, bioinformatics, 3'-UTR reporter assays, and RIP assays to identify miRNA targets.
- Gain- and loss-of-function studies in human skin organoids.
- Local delivery of miR-135a-3p inhibitors and mimics.
Main Results:
- miR-135a-3p was identified as an antiangiogenic miRNA that inhibits EC proliferation, migration, and tube formation.
- miR-135a-3p targets huntingtin-interacting protein 1 (HIP1), thereby inhibiting the p38 signaling pathway in ECs.
- Inhibition of miR-135a-3p in diabetic mice promoted wound healing by increasing angiogenesis and granulation tissue.
- Overexpression of miR-135a-3p impaired wound healing and angiogenesis.
Conclusions:
- miR-135a-3p is a critical regulator of pathophysiological angiogenesis and tissue repair.
- The VEGF-HIP1-p38 signaling axis is modulated by miR-135a-3p.
- Targeting miR-135a-3p offers a novel therapeutic strategy for enhancing tissue repair and treating angiogenic disorders.
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