Keratinocyte growth factor induces hyperproliferation and delays differentiation in a skin equivalent model system

被引:117
作者
Andreadis, ST
Hamoen, KE
Yarmush, ML
Morgan, JR
机构
[1] Shriners Burn Hosp, Boston, MA 02114 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Engn Med, Boston, MA 02114 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Surg Serv, Boston, MA 02114 USA
关键词
KGF; fibroblast growth factor; cell proliferation; rete ridges;
D O I
10.1096/fj.00-0324com
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Keratinocyte growth factor (KGF) is a paracrine mediator of epithelial cell growth. To examine the direct effects of KGF on the morphogenesis of the epidermis, we generated skin equivalents in vitro by seeding human keratinocytes on the papillary surface of acellular dermis and raising them up to the air-liquid interface. KGF was either added exogenously or expressed by keratinocytes via a recombinant retrovirus encoding KGF. KGF induced dramatic changes to the 3-dimensional organization of the epidermis including pronounced hyperthickening, crowding, and elongation of the basal cells, flattening of the rete ridges, and a ripple-like pattern in the junction of stratum corneum and granular layers. Quantitative immunostaining for the proliferation antigen, Ki67, revealed that in addition to increasing basal proliferation, KGF extended the proliferative compartment by inducing suprabasal cell proliferation. KGF also induced expression of the integrin alpha5 beta1 and delayed expression of keratin 10 and transglutaminase, However, barrier formation of the epidermis was not disrupted. These results demonstrate for the first time that a single growth factor can alter the 3-dimensional organization and proliferative function of an in vitro epidermis, In addition to new strategies for tissue engineering, such a well-defined system will be useful for analyzing growth factor effects on the complex links between cell proliferation, cell movement and differentiation within a stratified tissue.
引用
收藏
页码:898 / 906
页数:9
相关论文
共 44 条
[1]
KERATINOCYTE GROWTH-FACTOR - A FIBROBLAST GROWTH-FACTOR FAMILY MEMBER WITH UNUSUAL TARGET-CELL SPECIFICITY [J].
AARONSON, SA ;
BOTTARO, DP ;
MIKI, T ;
RON, D ;
FINCH, PW ;
FLEMING, TP ;
AHN, J ;
TAYLOR, WG ;
RUBIN, JS .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 638 :62-77
[2]
CTLA4Ig-mediated blockade of T-cell costimulation in patients with psoriasis vulgaris [J].
Abrams, JR ;
Lebwohl, MG ;
Guzzo, CA ;
Jegasothy, BV ;
Goldfarb, MT ;
Goffe, BS ;
Menter, A ;
Lowe, NJ ;
Krueger, G ;
Brown, MJ ;
Weiner, RS ;
Birkhofer, MJ ;
Warner, GL ;
Berry, KK ;
Linsley, PS ;
Krueger, JG ;
Ochs, HD ;
Kelley, SL ;
Kang, SW .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (09) :1243-1252
[3]
CHANGES IN KERATINOCYTE ADHESION DURING TERMINAL DIFFERENTIATION - REDUCTION IN FIBRONECTIN BINDING PRECEDES ALPHA-5-BETA-1-INTEGRIN LOSS FROM THE CELL-SURFACE [J].
ADAMS, JC ;
WATT, FM .
CELL, 1990, 63 (02) :425-435
[4]
FIBRONECTIN INHIBITS THE TERMINAL DIFFERENTIATION OF HUMAN KERATINOCYTES [J].
ADAMS, JC ;
WATT, FM .
NATURE, 1989, 340 (6231) :307-309
[5]
LIVING TISSUE FORMED INVITRO AND ACCEPTED AS SKIN-EQUIVALENT TISSUE OF FULL THICKNESS [J].
BELL, E ;
EHRLICH, HP ;
BUTTLE, DJ ;
NAKATSUJI, T .
SCIENCE, 1981, 211 (4486) :1052-1054
[6]
LIPID SUPPLEMENTED MEDIUM INDUCES LAMELLAR BODIES AND PRECURSORS OF BARRIER LIPIDS IN CULTURED ANALOGS OF HUMAN SKIN [J].
BOYCE, ST ;
WILLIAMS, ML .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 101 (02) :180-184
[7]
Surface electrical capacitance as a noninvasive index of epidermal barrier in cultured skin substitutes in athymic mice [J].
Boyce, ST ;
Supp, AP ;
Harriger, MD ;
Pickens, WL ;
Wickett, RR ;
Hoath, SB .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (01) :82-87
[8]
SUPPRESSION OF KERATINOCYTE GROWTH-FACTOR EXPRESSION BY GLUCOCORTICOIDS IN-VITRO AND DURING WOUND-HEALING [J].
BRAUCHLE, M ;
RASSLER, R ;
WERNER, S .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (04) :579-584
[9]
Transglutaminase 1 delivery to lamellar ichthyosis keratinocytes [J].
Choate, KA ;
Kinsella, TM ;
Williams, ML ;
Nolan, GP ;
Khavari, PA .
HUMAN GENE THERAPY, 1996, 7 (18) :2247-2253
[10]
Corrective gene transfer in the human skin disorder lamellar ichthyosis [J].
Choate, KA ;
Medalie, DA ;
Morgan, JR ;
Khavari, PA .
NATURE MEDICINE, 1996, 2 (11) :1263-1267