Skip to main content
Log in

Ability of various inserts to promote endothelium cell culture for the establishment of coculture models

  • Plenary lectures
  • Endothelial and smooth muscle cells
  • Published:
Cell Biology and Toxicology Aims and scope Submit manuscript

Abstract

To select an insert suitable for human umbilical vein endothelial cell (HUVEC) culture, we compared several available inserts of 0.2 to 0.45 μm porosity: Cellagen (ICN), Transwell-COL (Costar), Millicell-HA and CM (Millipore), Anopore (Nunc), Cyclopore (Falcon) in comparison with a control surface (Thermanox). The requirements were: (i) to promote attachment, adhesion and proliferation of HUVEC (judged by [3H]thymidine incorporation into DNA at days 1, 3, 7); (ii) to allow HUVEC visualization by inverted, fluorescence microscopy for uptake of DiI-Ac-LDL and scanning electron microscopy, performed at day 9 after seeding.

Because Transwell and Cellagen are collagen precoated and CM has to be coated for cell culture, we performed collagen coating (types I + III or IV) for non-pretreated inserts for the purpose of comparison. Our preferences comprise Transwell-COL, Cyclopore not coated or coated (whatever the collagen type), and Cellagen. However, on a quality/price ratio criterion, Cyclopore, even uncoated, is the insert of choice. The HA, CM and Anopore inserts, even coated, do not allow HUVEC growth but do not alter positive uptake of acetylated LDL.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

HUVEC:

human umbilical vein endothelial cells

References

  • Bordenave L, Baquey Ch, Bareille R et al. Endothelial cell compatibility testing of three different Pellethanes. J Biomed Mater Res. 1993a;27:1367–81.

    Google Scholar 

  • Bordenave L, Bareille R, Janvier G et al. Human tracheal epithelial cells in culture: a suitable model for testing the cytocompatibility of materials for endotracheal use. J Mater Sci: Mater Med. 1993b;4:327–36.

    Google Scholar 

  • Gallicchio M, Argyriou S, Ianches G et al. Stimulation of PAI-1 expression in endothelial cells by cultured vascular smooth-muscle cells. Arterioscler Thromb. 1994;14:815–23.

    Google Scholar 

  • Grosset C, Jazwiec B, Taupin JL et al. In vitro biosynthesis of leukemia inhibitory factor/human interleukin for DA cells by human endothelial cells: differential regulation by interleukin-1α and glucocorticoids. Blood. 1995;86:3763–70.

    Google Scholar 

  • Hauschka PV, Mavrakos AE, Iafrati MD, Doleman SE, Klasgsbrun M. Growth factors in bone matrix. J Biol Chem. 1986;261:12665–74.

    Google Scholar 

  • Jaffe EA, Nachman RL, Becher CG, Minick CR. Culture of human endothelial cells derived from umbilical veins. J Clin Invest. 1973;52:2745–56.

    Google Scholar 

  • Jurima-Romet M, Casley WL, Neu JM, Huang HS. Induction of CYP3A and associated terfenadine N-dealkylation in rat hepatocytes cocultured with 3T3 cells. Cell Biol Toxicol. 1995;11:313–27.

    Google Scholar 

  • Leavesley DI, Schwartz MA, Rosenfeld A, Cheresh DA. Integrin β1- and β3-mediated endothelial cell migration is triggered through distinct signaling mechanisms. J Cell Biol. 1993;121:163–70.

    Google Scholar 

  • Rémy M, Bordenave L, Bareille R et al. Endothelial cell compatibility testing of various prosthetic surfaces. J Mater Sci: Mater Med. 1994;5:808–12.

    Google Scholar 

  • Robert M, Noel-Hudson MS, Font J, Aubery M, Wepierre J. Influence of fibroblasts on epidermization by keratinocytes cultured on synthetic porous membrane (insert) at the air-liquid interface. Cell Biol Toxicol. 1994;10:361–5.

    Google Scholar 

  • Rubin LL, Hall DE, Porter S et al. A cell culture model of the blood brain barrier. J Cell Biol. 1991;115:1725–35.

    Google Scholar 

  • Sporn LA, Marder VJ, Wagner DD. Differing polarity of the constitutive and regulated secretory pathways for von Willebrand factor in endothelial cells. J Cell Biol. 1989;108:1283–9.

    Google Scholar 

  • Voyta JC, Via DP, Butterfield CE, Zetter BR. Identification and isolation of endothelial cells based on their increased uptake of acetylated-low density lipoprotein. J Cell Biol. 1984;99:2034–40.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Villars, F., Conrad, V., Rouais, F. et al. Ability of various inserts to promote endothelium cell culture for the establishment of coculture models. Cell Biol Toxicol 12, 207–214 (1996). https://doi.org/10.1007/BF00438147

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00438147

Keywords

Navigation