Retinal pigmented epithelium cultures on thermally responsive polymer porous substrates.

A cross-linkable co-polymer of UV-sensitive 4-(N-cinnamoylcarbamide)methylstyrene (CCMS) and N-isopropylacrylamide (NIPAAm), was applied to porous tissue culture inserts. Surface chemical analyses of the inserts show an introduction of a thermally responsive polymer comparable to that on similarly incorporated non-porous polystyrene surfaces. Contact angle measurements as well as atomic force microscopy show a surface change in response to changing temperature in an aqueous environment, from hydrophilic, extended polymer chains below 32 degrees C to a dense hydrophobic film above 32 degrees C. Cell growth on porous inserts allowed measurement of cell expression, such as transepithelial resistance and fluid transport, which are not observable on cells from non-porous surfaces. Cultures of retinal pigmented epithelium (RPE) were able to restore an environment similar to in vivo by forming a tight junction barrier membrane upon confluence at 37 degrees C, as observed by changes in morphology, transepithelial resistance, and directionally-specific fluid transport. In addition, cells cultured on these surfaces detached as an oriented polarized sheet when the inserts were brought to 20 degrees C. This cell sheet was transplanted to other tissue culture surface without polymer detachment or dissolution, or cell damage caused by traditional detachment methods using proteolytic enzymes.

[1]  P. Gouras,et al.  Synthesis of retinoids by human retinal epithelium and transfer to rod outer segments. , 1990, The Biochemical journal.

[2]  F. Mottram,et al.  Synthesis and fate of immunological surface receptors on cultured burkitt lymphoma cells , 1969, International journal of cancer.

[3]  P. Bernstein,et al.  A human retinal pigment epithelial cell line that retains epithelial characteristics after prolonged culture. , 1995, Investigative ophthalmology & visual science.

[4]  I. Grierson,et al.  Development, repair and regeneration of the retinal pigment epithelium , 1994, Eye.

[5]  J. Aubin,et al.  Microtubules, microfilaments and adhesion patterns in differentiating chick retinal pigment epithelial (RPE) cells in vitro. , 1983, Experimental cell research.

[6]  M. Boulton,et al.  Membrane-bound carbonic anhydrase in human retinal pigment epithelium. , 1994, Investigative ophthalmology & visual science.

[7]  T. Okano,et al.  Mechanism of cell detachment from temperature-modulated, hydrophilic-hydrophobic polymer surfaces. , 1995, Biomaterials.

[8]  T. Friberg,et al.  Effects of silicone oil and hyaluronic acid on cultured human retinal pigment epithelium. , 1990, Investigative ophthalmology & visual science.

[9]  J. Weiter,et al.  A photogrammetric method to measure fluid movement across isolated frog retinal pigment epithelium. , 1985, Biophysical journal.

[10]  T. Allen,et al.  The modulation of cellular contractility and adhesion by trypsin and EGTA. , 1980, Experimental cell research.

[11]  D. Bok,et al.  Polarized budding of vesicular stomatitis and influenza virus from cultured human and bovine retinal pigment epithelium. , 1992, Experimental eye research.

[12]  T. Okano,et al.  Novel thermally reversible hydrogel as detachable cell culture substrate. , 1998, Journal of biomedical materials research.

[13]  T. Okano,et al.  Thermo‐responsive polymeric surfaces; control of attachment and detachment of cultured cells , 1990 .

[14]  I. Constable,et al.  A simple flow cytometric technique to quantify rod outer segment phagocytosis in cultured retinal pigment epithelial cells. , 1996, Current eye research.

[15]  W. Green,et al.  Morphology of pig retinal pigment epithelium maintained in organ culture. , 1988, Archives of ophthalmology.

[16]  T. Okano,et al.  A novel recovery system for cultured cells using plasma-treated polystyrene dishes grafted with poly(N-isopropylacrylamide). , 1993, Journal of biomedical materials research.

[17]  I. Nabi,et al.  Immortalization of polarized rat retinal pigment epithelium. , 1993, Journal of cell science.

[18]  G. Eguchi,et al.  In vitro analysis of cellular metaplasia from pigmented epithelial cells to lens phenotypes: a unique model system for studying cellular and molecular mechanisms of "transdifferentiation". , 1986, Developmental biology.

[19]  D. Defoe,et al.  Reattachment of retinas to cultured pigment epithelial monolayers from Xenopus laevis. , 1994, Investigative ophthalmology & visual science.

[20]  A. Ben-Ze'ev,et al.  Cell-cell and cell-matrix interactions differentially regulate the expression of hepatic and cytoskeletal genes in primary cultures of rat hepatocytes. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[21]  P. Gouras,et al.  Retinoid metabolism in cultured human retinal pigment epithelium. , 1988, The Biochemical journal.

[22]  U. Vielkind,et al.  Evaluation of different procedures for the dissociation of retinal pigmented epithelium into single viable cells. , 1988, Pigment cell research.

[23]  S. Orgül,et al.  Osmotic stress in an in vitro model of the outer blood-retinal barrier. , 1993, German journal of ophthalmology.

[24]  L. Rizzolo The distribution of Na+,K(+)-ATPase in the retinal pigmented epithelium from chicken embryo is polarized in vivo but not in primary cell culture. , 1990, Experimental eye research.