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Microchannel Network Hydrogel Induced Ischemic Blood Perfusion Connection

Overview
Journal Nat Commun
Specialty Biology
Date 2020 Feb 1
PMID 32001693
Citations 28
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Abstract

Angiogenesis induction into damaged sites has long been an unresolved issue. Local treatment with pro-angiogenic molecules has been the most common approach. However, this approach has critical side effects including inflammatory coupling, tumorous vascular activation, and off-target circulation. Here, the concept that a structure can guide desirable biological function is applied to physically engineer three-dimensional channel networks in implant sites, without any therapeutic treatment. Microchannel networks are generated in a gelatin hydrogel to overcome the diffusion limit of nutrients and oxygen three-dimensionally. Hydrogel implantation in mouse and porcine models of hindlimb ischemia rescues severely damaged tissues by the ingrowth of neighboring host vessels with microchannel perfusion. This effect is guided by microchannel size-specific regenerative macrophage polarization with the consequent functional recovery of endothelial cells. Multiple-site implantation reveals hypoxia and neighboring vessels as major causative factors of the beneficial function. This technique may contribute to the development of therapeutics for hypoxia/inflammatory-related diseases.

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References
1.
Sooppan R, Paulsen S, Han J, Ta A, Dinh P, Gaffey A . In Vivo Anastomosis and Perfusion of a Three-Dimensionally-Printed Construct Containing Microchannel Networks. Tissue Eng Part C Methods. 2015; 22(1):1-7. PMC: 4722541. DOI: 10.1089/ten.TEC.2015.0239. View

2.
Simons M . Angiogenesis: where do we stand now?. Circulation. 2005; 111(12):1556-66. DOI: 10.1161/01.CIR.0000159345.00591.8F. View

3.
Sakai T, Hosoyamada Y . Are the precapillary sphincters and metarterioles universal components of the microcirculation? An historical review. J Physiol Sci. 2013; 63(5):319-31. PMC: 3751330. DOI: 10.1007/s12576-013-0274-7. View

4.
Jetten N, Verbruggen S, Gijbels M, Post M, de Winther M, Donners M . Anti-inflammatory M2, but not pro-inflammatory M1 macrophages promote angiogenesis in vivo. Angiogenesis. 2013; 17(1):109-18. DOI: 10.1007/s10456-013-9381-6. View

5.
Gardner A, Parker D, Montgomery P, Sosnowska D, Casanegra A, Ungvari Z . Gender and racial differences in endothelial oxidative stress and inflammation in patients with symptomatic peripheral artery disease. J Vasc Surg. 2014; 61(5):1249-57. PMC: 4185015. DOI: 10.1016/j.jvs.2014.02.045. View