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PMID: 15738680 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Diffusion limits of an in vitro thick prevascularized tissue.

Tissue engineering ·Vol. 11 ·No. 1-2 ·2005-00-00 ·Pages 257-66

Griffith CK, Miller C, Sainson RC, Calvert JW, Jeon NL, Hughes CC, George SC

Abstract

Although tissue engineering promises to replace or restore lost function to nearly every tissue in the body, successful applications are currently limited to tissue less than 2 mm in thickness. in vivo capillary networks deliver oxygen and nutrients to thicker (> 2 mm) tissues, suggesting that introduction of a preformed in vitro vascular network may be a useful strategy for engineered tissues. This article describes a system for generating capillary-like networks within a thick fibrin matrix. Human umbilical vein endothelial cells, growing on the surface of microcarrier beads, were embedded in fibrin gels a known distance (Delta = 1.8-4.5 mm) from a monolayer of human dermal fibroblasts. The distance of the growth medium, which contained vascular endothelial growth factor and basic fibroblast growth factor, from the beads, C, was varied from 2.7 to 7.2 mm. Capillaries with visible lumens sprouted in 2-3 days, reaching lengths that exceeded 500 microm within 6-8 days. On day 7, capillary network formation was largely independent of C; however, a strong inverse correlation with Delta was observed, with the maximum network formation at Delta = 1.8 mm. Surprisingly, the thickness of the gel was not a limiting factor for oxygen diffusion as these tissue constructs retained a relatively high oxygen tension of > 125 mmHg. We conclude that diffusion of oxygen in vitro is not limiting, allowing the development of tissue constructs on the order of centimeters in thickness. In addition, diffusion of fibroblast-derived soluble mediators is necessary for stable capillary formation, but is significantly impeded relative to that of nutrients present in the medium.

MeSH Terms
Capillaries/cytology,physiology Cell Culture Techniques/methods Cell Line Cells, Cultured Culture Media/chemistry Diffusion Endothelial Cells/cytology,drug effects Endothelium, Vascular/cytology Extracellular Matrix/metabolism Fibrin/metabolism Fibroblast Growth Factor 2/pharmacology Fibroblasts/cytology Gels Humans Models, Biological Neovascularization, Physiologic/physiology Oxygen/metabolism Skin/cytology Tissue Engineering/methods Umbilical Veins/cytology Vascular Endothelial Growth Factor A/pharmacology
Chemicals
Culture Media Gels Vascular Endothelial Growth Factor A Fibroblast Growth Factor 2 Fibrin Oxygen
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Griffith Craig K
Department of Biomedical Engineering, University of California, Irvine, Irvine, California 92697-2715, USA.
Miller Cheryl
Sainson Richard C A
Calvert Jay W
Jeon Noo Li
Hughes Christopher C W
George Steven C
Article Info
Journal
Tissue engineering
Abbr.
Tissue Eng
ISSN
1076-3279
Published
2005-00-00
Pages
257-66
Language
English
Region
United States
NLM ID
9505538
Subset
IM
Grants
NIAID NIH HHS · AI40710 · United States
NHLBI NIH HHS · HL60067 · United States
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