Either exogenous or endogenous fibronectin can promote adherence of human endothelial cells - PubMed (original) (raw)
Either exogenous or endogenous fibronectin can promote adherence of human endothelial cells
R A Clark et al. J Cell Sci. 1986 Jun.
Abstract
Recently, we have presented evidence that proliferating blood vessels produce and deposit fibronectin in situ during the angiogenesis of wound repair. This report extends these observations by demonstrating that human endothelial cells from both large and small vessels depend on fibronectin for their adherence in vitro. Endothelial cells were grown from human umbilical veins (HUVEC) by the method of Gimbrone and from the microvasculature of human omentum by the method of Kern, Knedler and Eckel. Second-passage cells were plated into microtitre wells that had been coated with 100 micrograms ml-1 of fibronectin, types I and III collagen, type IV collagen or laminin. After a 3-h incubation, adherent cells were solubilized with Zap-Isoton and quantified on a Coulter Counter. Under normal culture conditions HUVEC showed no preference for fibronectin substrates while microvascular cells always demonstrated a striking preference for fibronectin substrates. However, when HUVEC were exposed to 2.5 or 25 micrograms ml-1 of cycloheximide for 4 h before and during the adherence assays, the adherence to fibronectin was 50-200% greater than to types I and III collagen. Immunofluorescence studies showed that while HUVEC expressed a large quantity of surface fibronectin, microvascular cells expressed very little. Metabolic labelling studies confirmed that HUVEC cultures had substantial quantities of fibronectin in their cell layer while microvascular cells did not. In antibody blocking experiments, preincubation of fibronectin-coated surfaces with anti-fibronectin antibodies totally blocked microvascular cell adhesion but only abrogated HUVEC adherence by 50%, presumably since these latter cells were able to deposit additional fibronectin onto the surface during the 3 h assay period. In the presence of cycloheximide anti-fibronectin antibodies totally blocked HUVEC adherence. These results demonstrate that both endothelial cell types rely, at least in part, on fibronectin for adherence in vitro. HUVEC can synthesize, secrete and deposit enough fibronectin for their adherence in vitro, while microvascular cells rely on an exogenous source of fibronectin under these culture conditions. Thus, the increased blood vessel fibronectin observed during angiogenesis in vivo may mediate adherence of the proliferating and migrating endothelial cells.
Similar articles
- Cytoskeletal changes induced by excess extracellular matrix impair endothelial cell replication.
Podestá F, Roth T, Ferrara F, Cagliero E, Lorenzi M. Podestá F, et al. Diabetologia. 1997 Aug;40(8):879-86. doi: 10.1007/s001250050763. Diabetologia. 1997. PMID: 9267981 - Fibronectin, as well as other extracellular matrix proteins, mediate human keratinocyte adherence.
Clark RA, Folkvord JM, Wertz RL. Clark RA, et al. J Invest Dermatol. 1985 May;84(5):378-83. doi: 10.1111/1523-1747.ep12265466. J Invest Dermatol. 1985. PMID: 2582060 - Endothelial cells adherent to expanded polytetrafluoroethylene express the intercellular adhesion molecule-1.
Margiotta MS, Benton L, Greco RS. Margiotta MS, et al. J Am Coll Surg. 1995 Sep;181(3):215-9. J Am Coll Surg. 1995. PMID: 7670680 - Fibronectin mediates adherence of rat alveolar type II epithelial cells via the fibroblastic cell-attachment domain.
Clark RA, Mason RJ, Folkvord JM, McDonald JA. Clark RA, et al. J Clin Invest. 1986 Jun;77(6):1831-40. doi: 10.1172/JCI112509. J Clin Invest. 1986. PMID: 3519680 Free PMC article.
Cited by
- An important step towards a prevascularized islet microencapsulation device: in vivo prevascularization by combination of mesenchymal stem cells on micropatterned membranes.
Groot Nibbelink M, Skrzypek K, Karbaat L, Both S, Plass J, Klomphaar B, van Lente J, Henke S, Karperien M, Stamatialis D, van Apeldoorn A. Groot Nibbelink M, et al. J Mater Sci Mater Med. 2018 Nov 9;29(11):174. doi: 10.1007/s10856-018-6178-6. J Mater Sci Mater Med. 2018. PMID: 30413974 Free PMC article. - A microfluidic platform for modeling metastatic cancer cell matrix invasion.
Blaha L, Zhang C, Cabodi M, Wong JY. Blaha L, et al. Biofabrication. 2017 Sep 1;9(4):045001. doi: 10.1088/1758-5090/aa869d. Biofabrication. 2017. PMID: 28812983 Free PMC article. - Immune Complex-Induced, Nitric Oxide-Mediated Vascular Endothelial Cell Death by Phagocytes Is Prevented with Decoy FcγReceptors.
Mula RV, Machiah D, Holland L, Wang X, Parihar H, Sharma AC, Selvaraj P, Shashidharamurthy R. Mula RV, et al. PLoS One. 2016 Apr 21;11(4):e0153620. doi: 10.1371/journal.pone.0153620. eCollection 2016. PLoS One. 2016. PMID: 27101012 Free PMC article. - Elastofibroma dorsi: a histochemical and immunohistochemical study.
Di Vito A, Scali E, Ferraro G, Mignogna C, Presta I, Camastra C, Donato G, Barni T. Di Vito A, et al. Eur J Histochem. 2015 Feb 19;59(1):2459. doi: 10.4081/ejh.2015.2459. Eur J Histochem. 2015. PMID: 25820560 Free PMC article. - Adhesion of endothelial cells and endothelial progenitor cells on peptide-linked polymers in shear flow.
Wang X, Cooper S. Wang X, et al. Tissue Eng Part A. 2013 May;19(9-10):1113-21. doi: 10.1089/ten.TEA.2011.0653. Epub 2013 Jan 30. Tissue Eng Part A. 2013. PMID: 23167808 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources