## Abstract Endothelial cells derived from human pulmonary arteries incorporate (^3^H)โglucosamine and ^35^SO~4~ into glycosaminoglycans and into the carbohydrate side chains of glycoproteins. These ^3^H/^35^Sโcarbohydrate chains were isolated from cells and culture medium after Pronase digestion.
Distinct extracellular matrix microenvironments of progenitor and carotid endothelial cells
โ Scribed by Keri B. Vartanian; Sean J. Kirkpatrick; Owen J. T. McCarty; Tania Q. Vu; Stephen R. Hanson; Monica T. Hinds
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 613 KB
- Volume
- 91A
- Category
- Article
- ISSN
- 1549-3296
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โฆ Synopsis
Abstract
Endothelial cells (ECs) produce and maintain the local extracellular matrix (ECM), a critical function that contributes to EC and blood vessel health. This function is also crucial to vascular tissue engineering, where endothelialization of vascular constructs require a cell source that readily produces and maintains ECM. In this study, baboon endothelial progenitor cell (EPC) deposition of ECM (laminin, collagen IV, and fibronectin) was characterized and compared to mature carotid ECs, evaluated in both elongated and cobblestone morphologies typically found in vivo. Microfluidic micropatterning was used to create 15โฮผm wide adhesive lanes with 45โฮผm spacing to reproduce the elongated EC morphology without the influence of external forces. Both EPCs and ECs elongated on micropatterned lanes had aligned actin cytoskeleton and readily deposited ECM. EPCs deposited and remodeled the ECM to a greater extent than ECs. Since a readily produced ECM can improve graft patency, EPCs are an advantageous cell source for endothelializing vascular constructs. Furthermore, EC deposition of ECM was dependent on cell morphology, where elongated ECs deposited more collagen IV and less fibronectin compared to matched cobblestone controls. Thus micropatterned surfaces controlled EC shape and ECM deposition, which ultimately has implications for the design of tissueโengineered vascular constructs. ยฉ 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009
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