Identification of macrophage migration inhibitory factor (MIF) in human skin and its immunohistochemical localization

被引:129
作者
Shimizu, T
Ohkawara, A
Nishihira, J
Sakamoto, W
机构
[1] HOKKAIDO UNIV,SCH MED,CANC RES INST,SAPPORO,HOKKAIDO 060,JAPAN
[2] HOKKAIDO UNIV,SCH MED,DEPT DERMATOL,SAPPORO,HOKKAIDO 060,JAPAN
[3] HOKKAIDO UNIV,SCH DENT,DEPT BIOCHEM,SAPPORO,HOKKAIDO 060,JAPAN
关键词
human skin; immunohistochemistry; keratinocyte; macrophage migration inhibitory factor; reverse transcription-polymerase chain reaction;
D O I
10.1016/0014-5793(96)00120-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The presence and tissue localization of macrophage migration inhibitory factor (MIF) in human skin were examined, Reverse transcription-polymerase chain reaction analysis revealed that MIF mRNA was expressed in both surgically obtained normal human epidermis and primary cultured human keratinocytes. The expression of MIF was further confirmed by Western blot analysis, which demonstrated a single band at about 12.5 kDa using a polyclonal antibody against human recombinant MIF. Immunohistochemical studies showed that MIF existed in human epidermis, especially in the basal layer, The pathophysiological role of MIF in human skin remains undefined; however, the present results indicate that MIF may play an important role in immunity, inflammation and cellular differentiation of epidermal cells.
引用
收藏
页码:199 / 202
页数:4
相关论文
共 19 条
[1]   KERATINOCYTES AS INITIATORS OF INFLAMMATION [J].
BARKER, JNWN ;
MITRA, RS ;
GRIFFITHS, CEM ;
DIXIT, VM ;
NICKOLOFF, BJ .
LANCET, 1991, 337 (8735) :211-214
[2]   MIF IS A PITUITARY-DERIVED CYTOKINE THAT POTENTIATES LETHAL ENDOTOXEMIA [J].
BERNHAGEN, J ;
CALANDRA, T ;
MITCHELL, RA ;
MARTIN, SB ;
TRACEY, KJ ;
VOELTER, W ;
MANOGUE, KR ;
CERAMI, A ;
BUCALA, R .
NATURE, 1993, 365 (6448) :756-759
[3]   MECHANISM OF A REACTION IN VITRO ASSOCIATED WITH DELAYED-TYPE HYPERSENSITIVITY [J].
BLOOM, BR ;
BENNETT, B .
SCIENCE, 1966, 153 (3731) :80-&
[4]   MACROPHAGE IS AN IMPORTANT AND PREVIOUSLY UNRECOGNIZED SOURCE OF MACROPHAGE-MIGRATION INHIBITORY FACTOR [J].
CALANDRA, T ;
BERNHAGEN, J ;
MITCHELL, RA ;
BUCALA, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (06) :1895-1902
[5]   MIF AS A GLUCOCORTICOID-INDUCED MODULATOR OF CYTOKINE PRODUCTION [J].
CALANDRA, T ;
BERNHAGEN, J ;
METZ, CN ;
SPIEGEL, LA ;
BACHER, M ;
DONNELLY, T ;
CERAMI, A ;
BUCALA, R .
NATURE, 1995, 377 (6544) :68-71
[6]   KERATINOCYTE GROWTH-REGULATION BY THE PRODUCTS OF IMMUNE CELLS [J].
HANCOCK, GE ;
KAPLAN, G ;
COHN, ZA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (04) :1395-1402
[7]   INTERLEUKIN-1 IS PROCESSED AND RELEASED DURING APOPTOSIS [J].
HOGQUIST, KA ;
NETT, MA ;
UNANUE, ER ;
CHAPLIN, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8485-8489
[8]   HUMAN KERATINOCYTES ARE A SOURCE FOR TUMOR-NECROSIS-FACTOR-ALPHA - EVIDENCE FOR SYNTHESIS AND RELEASE UPON STIMULATION WITH ENDOTOXIN OR ULTRAVIOLET-LIGHT [J].
KOCK, A ;
SCHWARZ, T ;
KIRNBAUER, R ;
URBANSKI, A ;
PERRY, P ;
ANSEL, JC ;
LUGER, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (06) :1609-1614
[9]   INTERLEUKIN-1 GENE-EXPRESSION IN CULTURED HUMAN KERATINOCYTES IS AUGMENTED BY ULTRAVIOLET-IRRADIATION [J].
KUPPER, TS ;
CHUA, AO ;
FLOOD, P ;
MCGUIRE, J ;
GUBLER, U .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (02) :430-436
[10]  
NISHIHIRA J, 1993, BIOCHEM MOL BIOL INT, V31, P841