LOCALIZATION OF INTERLEUKIN-1-BETA IN HUMAN PERIODONTAL TISSUE

被引:102
作者
JANDINSKI, JJ
STASHENKO, P
FEDER, LS
LEUNG, CC
PEROS, WJ
RYNAR, JE
DEASY, MJ
机构
[1] BIOTECH DIAGNOST,CAMBRIDGE,MA
[2] UNIV MED & DENT NEW JERSEY,DEPT BIOL,NEWARK,NJ 07103
[3] UNIV MED & DENT NEW JERSEY,DEPT DIAGNOST SCI,NEWARK,NJ 07103
[4] UNIV MED & DENT NEW JERSEY,DEPT ANAT,NEWARK,NJ 07103
[5] UNIV MED & DENT NEW JERSEY,DEPT PERIODONTOL,NEWARK,NJ 07103
[6] FORSYTH DENT CTR,DEPT IMMUNOL,BOSTON,MA 02115
关键词
INTERLEUKIN-1-BETA; PERIODONTAL DISEASES PATHOGENESIS;
D O I
10.1902/jop.1991.62.1.36
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
INTERLEUKIN-1-beta (IL-1-beta) IS THE PREDOMINANT FORM OF IL-1 produced by macrophages. IL-1-beta possesses numerous and diverse biological activities. Several of these activities, including fibroblast proliferation, potentiation of the immune response, and stimulation of bone resorption may be of relevance to the pathogenesis of periodontal disease. This study was designed to examine the presence of IL-1-beta in human periodontal tissue. An antiserum directed against the N-terminal segment (117-131) of human IL-1-beta was used to detect IL-1-beta using immunofluorescent staining techniques. IL-1-beta positive staining cells were observed in both normal and diseased tissue and were limited to the lamina propria. Brightly staining cells were increased by almost 3-fold in periodontally diseased tissue when compared to normal tissue. Low intensity staining cells were equally distributed in the normal and diseased specimens. We propose that IL-1-beta and IL-1-beta produced by cells in periodontal tissues may be related to the pathological processes associated with periodontal disease.
引用
收藏
页码:36 / 43
页数:8
相关论文
共 29 条
[1]  
ANSEL JC, 1988, J IMMUNOL, V140, P1174
[2]   FIBROBLASTIC SUBPOPULATIONS IN UNINJURED AND WOUNDED RABBIT ORAL-MUCOSA [J].
BRONSON, RE ;
TREAT, JA ;
BERTOLAMI, CN .
JOURNAL OF DENTAL RESEARCH, 1989, 68 (01) :51-58
[3]   INCREASED THYMOCYTE-ACTIVATING FACTOR IN HUMAN GINGIVAL FLUID DURING GINGIVAL INFLAMMATION [J].
CHARON, JA ;
LUGER, TA ;
MERGENHAGEN, SE ;
OPPENHEIM, JJ .
INFECTION AND IMMUNITY, 1982, 38 (03) :1190-1195
[4]  
DEWHIRST FE, 1985, J IMMUNOL, V135, P2562
[5]   BIOLOGY OF INTERLEUKIN-1 [J].
DINARELLO, CA .
FASEB JOURNAL, 1988, 2 (02) :108-115
[6]  
ENGVALL E, 1972, J IMMUNOL, V109, P129
[7]  
GERY I, 1984, LYMPHOKINES, V9, P109
[8]   IS SECRETED IL-1 NECESSARY FOR NORMAL HUMAN T-CELL ACTIVATION [J].
GOEKEN, NE ;
STAGGS, TS .
HUMAN IMMUNOLOGY, 1988, 21 (02) :99-113
[9]   AN INTERLEUKIN-1 LIKE FACTOR STIMULATES BONE-RESORPTION INVITRO [J].
GOWEN, M ;
WOOD, DD ;
IHRIE, EJ ;
MCGUIRE, MKB ;
RUSSELL, RGG .
NATURE, 1983, 306 (5941) :378-380
[10]   BACTEROIDES-GINGIVALIS FIMBRIAE STIMULATE PRODUCTION OF THYMOCYTE-ACTIVATING FACTOR BY HUMAN GINGIVAL FIBROBLASTS [J].
HANAZAWA, S ;
HIROSE, K ;
OHMORI, Y ;
AMANO, S ;
KITANO, S .
INFECTION AND IMMUNITY, 1988, 56 (01) :272-274