Journal of Investigative Dermatology (1996) 106, 287–293; doi:10.1111/1523-1747.ep12340722
The Derivation and Characterization of Pig Keratinocyte Cell Lines That Retain the Ability to Differentiate
Ulrich R Hengge1, Edward F Chan1, Victoria Hampshire2, Ruth A Foster1 and Jonathan C Vogel1
- 1Dermatology Branch, National Cancer Institute, National Institutes of Health (NIH), NIH, Bethesda, Maryland, U.S.A.
- 2National Center for Research Resources, Veterinary Resources Program, National Institutes of Health (NIH), NIH, Bethesda, Maryland, U.S.A.
Received 28 May 1995; Revised 29 September 1995; Accepted 11 October 1995.
Top of pageAbstract
Pig skin may be a very useful model for studying human skin biology, since its morphology closely resembles that of human skin. To manipulate pig keratinocytes in vitro, we have analyzed different culture conditions for optimal pig keratinocyte growth and describe here a simple method for culture and extended passage of primary pig keratinocytes on collagen substrates. The colony-forming efficiency and proliferative capacity of primary pig keratinocytes were readily supported by Type I collagen and a final calcium concentration of 0.075 mM. These culture conditions permitted efficient gene transfer into keratinocytes using various cationic lipids at a 4:1 ratio (lipid:DNA). In addition, immortalized pig keratinocyte cell lines, which maintained a normal phenotype, were derived using these optimized culture conditions. By karyotype analysis, two independently derived cell lines had the same chromosomal abnormalities, suggesting a causal role in their immortalization. The keratinocyte cell lines exhibited a differentiated phenotype in response to elevated calcium concentration and were nontumorigenic in in vivo tumor assays. Immortalized pig keratinocyte cell lines that maintain the ability to differentiate may become a valuable tool in the study of epidermal differentiation both in vitro and in vivo. In addition, methods using keratinocytes to deliver genes to pigs in vivo could also be enhanced with these pig keratinocyte cell lines.
Keywords:
-galactosidase, Collagen, differentiation, gene transfer
Top of pageReferences
- Barrandon, Y, Green, H: Cell migration is essential for sustained growth of keratinocyte colonies. The roles of transforming growth factor-
and epidermal growth factor. Cell 50: 1131–1137, 1987 | Article | PubMed | ISI | ChemPort | - Boukamp, P, Petrussevska, RT, Breitkreutz, D, Hornung, J, Markham, A, Fusenig, NE: Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line. J Cell Biol 106: 761–771, 1988 | Article | PubMed | ISI | ChemPort |
- Boyce, ST, Ham, RH: Calcium-regulated differentiation of normal human epidermal keratinocytes in chemically defined clonal culture and serum-free serial culture. J Invest Dermatol 81: s33–s40, 1983
- Brans, TA, Dutrieux, RP, Hockstra, MJ, Kreis, RW, Du Pont, JS: Histopathological evaluation of scalds and contact burns in the pig model. Burns 20: S48–S51, 1994
- Ding, YL, Pu, SS, Wu, DZ, Ma, C, Pan, ZL, Lu, X, Miro, SG, Yao, ZX, He, J: Clinical and histological observations on the application of intermingled auto- and pig-skin heterografts in third degree burns. Burns Incl Therm Inj 9: 381–386, 1993
- Gailit, JO, Clark, RA: Integrins. Adv Dermatol 8: 129–152, 1993
- Gallico, GG, O'Connor, NE, Compton, CC, Kehinde, O, Green, H: Permanent coverage of large burn wounds with autologous cultured human epithelium. N Engl J Med 311: 448–451, 1984 | PubMed | ISI |
- Garlick, JA, Taichman, LB: Fate of human keratinocytes during reepithelialization in an organotypic culture model. Lab Invest 70: 916–922, 1994 | PubMed | ISI | ChemPort |
- Gustavsson, I: Standard karyotype of the domestic pig. Hereditas 109: 151–157, 1988
- Hengge, UR, Chan, EF, Foster, RA, Walker, PS, Vogel, JC: Cytokine gene expression in epidermis with biological effects following injection of naked DNA. Nature Genet 10: 161–166, 1995 | Article |
- Hennings, H, Michael, D, Cheng, C, Steinert, P, Holbrook, KA, Yuspa, SH: Calcium regulation of growth and differentiation of mouse epidermal cells in culture. Cell 19: 245–254, 1980 | Article | PubMed | ISI | ChemPort |
- Jain, V, Magrath, I: A chemiluminescent assay for quantitation of
-galactosidase in the femtogram range: application to quantitation of
-galactosidase in lacZ-transfected cells. Anal Biochem 199: 119–124, 1991 | PubMed | - Jones, PH, Harper, S, Watt, FM: Stem cell patterning and fate in human epidermis. Cell 80: 83–93, 1995 | Article | PubMed | ISI | ChemPort |
- Jones, PH, Watt, FM: Separation of human epidermal stem cells from transit amplifying cells on the basis of differences in integrin function and expression. Cell 73: 713–724, 1993 | Article | PubMed | ISI | ChemPort |
- Joshi, MS: Growth and differentiation of the cultured secretory cells of the cow oviduct on reconstituted basement membrane. J Exp Zool 260: 229–238, 1991
- Kangesu, T, Navsaria, HA, Manek, S, Shurey, CB, Jones, CR, Fryer, PR, Leigh, IM, Green, CJ: A pig model using skin graft chambers for studies on cultured keratinocytes. Br J Plast Surg 46: 393–400, 1993
- King, IA, Tabiowo, A, Fryer, PR, Purkis, PE, Leigh, I: Basal cell glycoprotein in pig epidermis closely resembles the beta-1 subunit of the integrin family of cell adhesion molecules. J Invest Dermatol 97: 501–505, 1991
- MacGregor, GR, Nolan, GR, Fiering, S, Roederer, M, Herzenberg, LA: Use of E. coli IacZ (
-Galactosidase) as a reporter gene. In: Murray EJ, Walker JM (eds.). Gene Expression in Vivo Humana Press, Clifton, pp 217–237, 1989 - Pescovitz, MD, Hsu, SM, Katz, SI, Lunney, JK, Shimada, S, Sachs, DH: Characterization of a porcine CDI-specific mAb that distinguishes CD4/CD8 double-positive thymic from peripheral T lymphocytes. Tissue Antigens 34: 151–156, 1990
- Peterson, WD, Simpson, WF, Hukku, B: Cell culture characterization: monitoring for cell identification. In: Jakoby WB, Pasten IH (eds.). Methods in Enzymology Vol. 58: Academic Press, San Diego, pp 164–178, 1979
- Quaglino, D, Nanney, LB, Ditesheim, JA, Davidson, JM: Transforming growth factorbeta stimulates wound healing and modulates extracellular matrix gene expression in pig skin: incisional wound model. J Invest Dermatol 97: 34–42, 1991 | PubMed | ISI | ChemPort |
- Regauer, S, Compton, CC: Cultured pig epithelial grafts: an improved method. J Invest Dermatol 94: 230–234, 1990
- Rheinwald, JG, Green, H: Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells. Cell 6: 331–334, 1975 | Article | PubMed | ISI | ChemPort |
- Rigal, C, Pieraggi, MT, Vincent, C, Prost, C, Bouissou, H, Serre, G: Healing of full-thickness wounds in the pig. I. Immunohistochemical study of epidermo-dermal junction regeneration. J Invest Dermatol 96: 777–785, 1991 | PubMed | ISI | ChemPort |
- Sachs, DH, Leight, G, Cone, J, Schwarz, S, Stuart, L, Rosenberg, S: Transplantation in miniature swine. I. Fixation of the major histocompatibility complex. Transplantation 22: 559–567, 1976 | PubMed | ISI | ChemPort |
- Seabright, M: A rapid banding technique for human chromosomes. Lancet 2: 971–972, 1971 | Article | PubMed | ISI | ChemPort |
- Sieber, VK, Wilkinson, J, Aluri, GR, Bywaters, T: Quantification of radiation-induced epilation in the pig: a biological indicator of radiation dose to the skin. Int J Radial Biol 63: 355–360, 1993
- Staedel, C, Remy, JS, Hua, Z, Broker, TR, Chow, LT, Behr, JP: High-efficiency transfection of primary human keratinocytes with positively charged lipopolyamine:DNA complexes. J Invest Dermatol 102: 768–772, 1994 | Article | PubMed | ChemPort |
- Tsao, MC, Walthall, BJ, Ham, RG: Clonal growth of normal human epidermal keratinocytes in a defined medium. J Cell Physiol 110: 219–229, 1982 | Article | PubMed | ISI | ChemPort |
- Vogt, PM, Thompson, S, Andree, C, Liu, P, Breuing, K, Hatzis, D, Brown, H, Mulligan, RC, Eriksson, E: Genetically modified keratinocytes transplanted to wounds reconstitute the epidermis. Proc Natl Acad Sci USA 91: 9307–9311, 1994 | PubMed | ChemPort |