In vitro microvessels for the study of angiogenesis and thrombosis

Authors
Zheng, YingChen, JunmeiCraven, MichaelChoi, Nak WonTotorica, SamuelDiaz-Santana, AnthonyKermani, PounehHempstead, BarbaraFischbach-Teschl, ClaudiaLopez, Jose A.Stroock, Abraham D.
Issue Date
2012-06-12
Publisher
NATL ACAD SCIENCES
Citation
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, v.109, no.24, pp.9342 - 9347
Abstract
Microvascular networks support metabolic activity and define microenvironmental conditions within tissues in health and pathology. Recapitulation of functional microvascular structures in vitro could provide a platform for the study of complex vascular phenomena, including angiogenesis and thrombosis. We have engineered living microvascular networks in three-dimensional tissue scaffolds and demonstrated their biofunctionality in vitro. We describe the lithographic technique used to form endothelialized microfluidic vessels within a native collagen matrix; we characterize the morphology, mass transfer processes, and long-termstability of the endothelium; we elucidate the angiogenic activities of the endothelia and differential interactions with perivascular cells seeded in the collagen bulk; and we demonstrate the nonthrombotic nature of the vascular endothelium and its transition to a prothrombotic state during an inflammatory response. The success of these microvascular networks in recapitulating these phenomena points to the broad potential of this platform for the study of cardiovascular biology and pathophysiology.
Keywords
ENDOTHELIAL CELL MORPHOLOGY; EVANS-BLUE UPTAKE; THROMBOCYTOPENIC PURPURA; PLATELET-ADHESION; FACTOR MULTIMERS; SHEAR-STRESS; TISSUE; PERMEABILITY; CANCER; MECHANISMS; ENDOTHELIAL CELL MORPHOLOGY; EVANS-BLUE UPTAKE; THROMBOCYTOPENIC PURPURA; PLATELET-ADHESION; FACTOR MULTIMERS; SHEAR-STRESS; TISSUE; PERMEABILITY; CANCER; MECHANISMS; tissue engineering; regenerative medicine; microfluidics; cancer; blood
ISSN
0027-8424
URI
https://pubs.kist.re.kr/handle/201004/129148
DOI
10.1073/pnas.1201240109
Appears in Collections:
KIST Article > 2012
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