Interleukin-1 induces transcription of keratin K6 in human epidermal keratinocytes

被引:85
作者
Komine, M
Rao, LS
Freedberg, IM
Simon, M
Milisavljevic, V
Blumenberg, M
机构
[1] NYU, Med Ctr, Ronald O Perelman Dept Dermatol, Dept Cell Biol, New York, NY 10016 USA
[2] NYU, Med Ctr, Dept Biochem, New York, NY 10016 USA
[3] NYU, Med Ctr, Kaplan Canc Res Ctr, New York, NY 10016 USA
[4] SUNY Stony Brook, Dept Oral Biol & Pathol, Dept Dermatol & Living Skin Bank, Stony Brook, NY 11794 USA
关键词
C/EBP beta; inflammation; nuclear factor NF kappa B; organ culture; transcriptional regulation;
D O I
10.1046/j.1523-1747.2001.01249.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Keratinocytes respond to injury by releasing the proinflammatory cytokine interleukin-1, which serves as the initial "alarm signal" to surrounding cells. Among the consequences of interleukin-1 release is the production of additional cytokines and their receptors by keratinocytes and other cells in the skin. Here we describe an additional effect of interleukin-1 on keratinocytes, namely the alteration in the keratinocyte cytoskeleton in the form of the induction of keratin 6 expression. Keratin 6 is a marker of hyperproliferative, activated keratinocytes, found in wound healing, psoriasis, and other inflammatory disorders. Skin biopsies in organ culture treated with interleukin-1 express keratin 6 in all suprabasal layers of the epidermis, throughout the tissue. In cultured epidermal keratinocytes, the induction of keratin 6 is time and concentration dependent. Importantly,1, subconfluent cultures do not. In the cells starved of growth factors, epidermal growth factor or tumor necrosis factor-alpha, if added simultaneously with interleukin-1, they synergistically augment the effects of interleukin-1. Using DNA-mediated cell transfection, we analyzed the molecular mechanisms regulating the keratin 6 induction by interleukin-1, and found that the induction occurs at the transcriptional level. We used a series of deletions and point mutations to identify the interleukin-1 responsive DNA element in the keratin 6 promoter, and determined that it contains a complex of C/EBP binding sites. The transcription factor C/EBP beta binds this element in vitro, and the binding is augmented by pretreatment of the cells with interleukin-1. The interleukin-1 responsive element is clearly distinct from the epidermal growth factor responsive one, which means that the proinflammatory and proliferative signals independently regulate the expression of keratin 6. Thus, interleukin-1 initiates keratinocyte activation not only by triggering additional signaling events, but also by inducing directly the synthesis of keratin 6 in epidermal keratinocytes, and thus changing the composition of their cytoskeleton.
引用
收藏
页码:330 / 338
页数:9
相关论文
共 50 条
[1]   A NUCLEAR FACTOR FOR IL-6 EXPRESSION (NF-IL6) IS A MEMBER OF A C/EBP FAMILY [J].
AKIRA, S ;
ISSHIKI, H ;
SUGITA, T ;
TANABE, O ;
KINOSHITA, S ;
NISHIO, Y ;
NAKAJIMA, T ;
HIRANO, T ;
KISHIMOTO, T .
EMBO JOURNAL, 1990, 9 (06) :1897-1906
[2]   KERATINOCYTES AS INITIATORS OF INFLAMMATION [J].
BARKER, JNWN ;
MITRA, RS ;
GRIFFITHS, CEM ;
DIXIT, VM ;
NICKOLOFF, BJ .
LANCET, 1991, 337 (8735) :211-214
[3]  
Bernerd Francoise, 1993, Gene Expression, V3, P187
[4]   EFFECT OF GROWTH-FACTORS ON CELL-PROLIFERATION AND EPITHELIALIZATION IN HUMAN SKIN [J].
BHORA, FY ;
DUNKIN, BJ ;
BATZRI, S ;
ALY, HM ;
BASS, BL ;
SIDAWY, AN ;
HARMON, JW .
JOURNAL OF SURGICAL RESEARCH, 1995, 59 (02) :236-244
[5]  
BIRD TA, 1989, J IMMUNOL, V142, P126
[6]   MUTATION OF A TYPE-II KERATIN GENE (K6A) IN PACHYONYCHIA-CONGENITA [J].
BOWDEN, PE ;
HALEY, JL ;
KANSKY, A ;
ROTHNAGEL, JA ;
JONES, DO ;
TURNER, RJ .
NATURE GENETICS, 1995, 10 (03) :363-365
[7]   A FAMILY OF CONSTITUTIVE C/EBP-LIKE DNA-BINDING PROTEINS ATTENUATE THE IL-1-ALPHA INDUCED, NF-KAPPA-B MEDIATED TRANSACTIVATION OF THE ANGIOTENSINOGEN GENE ACUTE-PHASE RESPONSE ELEMENT [J].
BRASIER, AR ;
RON, D ;
TATE, JE ;
HABENER, JF .
EMBO JOURNAL, 1990, 9 (12) :3933-3944
[8]   TARF6 is a signal transducer for interleukin-1 [J].
Cao, ZD ;
Xiong, J ;
Takeuchi, M ;
Kurama, T ;
Goeddel, DV .
NATURE, 1996, 383 (6599) :443-446
[9]  
DICKINSON AM, 1994, BONE MARROW TRANSPL, V13, P65
[10]  
DINARELLO CA, 1993, NEW ENGL J MED, V328, P106