The immunohistochemical localization of signal-transduction pathway components JAK1, JAK2, JAK3, TYK2 and STAT-1 during early enamel and dentine formation in rat molars

被引:13
作者
Tanase, S
Bawden, JW
机构
[1] UNIV N CAROLINA, DEPT PEDIAT DENT, CHAPEL HILL, NC 27599 USA
[2] ASAHI UNIV, SCH DENT, DEPT PEDIAT DENT, GIFU 50102, JAPAN
关键词
enamel; amelogenesis; dentine; dentinogenesis; signal transduction; cytokine; JAK; STAT; rat molar;
D O I
10.1016/S0003-9969(96)00048-9
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
This study sought to localize immunohistochemically Janus kinase (Jak) and Tyk isoforms and STAT-1 in association with events involved in early dentine and enamel formation in the rat molar. The Jaks and STATs (signal transducers and activators of transcription) are key signal-transduction pathway components in the cytokine receptor-linked pathway. The histological sections were not demineralized or fixed, providing optimum conditions for immunohistochemical localization. It appears that all of the Jak isoforms and STAT-1 are involved in enamel formation. Jak2 and STAT-1 colocalized in the proximal ends of presecretory and secretory-stage ameloblasts, supporting work by others that growth hormone receptor is located at that site. The colocalization of Jak1, Jak2 and STAT-1 along the proximal ends of presecretory and secretory ameloblasts suggests that the interferon receptor is up-regulated in these cells as well. Also, colocalization of Jak3 and STAT-1 in the proximal ends of the ameloblasts and the cells of the stratum intermedium predicts the location of the interleukin-7 receptor in those locations. Jak1, Tyk2 and STAT-1, but not Jak2 or Jak3, stain was seen in the odontoblasts. Copyright (C) 1997 Published by Elsevier Science Ltd.
引用
收藏
页码:925 / 940
页数:16
相关论文
共 27 条
[1]   DISTRIBUTION OF PROTEIN-KINASE CA AND ACCUMULATION OF EXTRACELLULAR CA2+ DURING EARLY DENTIN AND ENAMEL FORMATION [J].
BAWDEN, JW ;
ROZELL, B ;
WURTZ, T ;
FOUDA, N ;
HAMMARSTROM, L .
JOURNAL OF DENTAL RESEARCH, 1994, 73 (08) :1429-1436
[2]  
BUSTELO XR, 1993, CELL GROWTH DIFFER, V4, P297
[3]   ACTIVATION OF ACUTE-PHASE RESPONSE FACTOR (APRF)/STAT3 TRANSCRIPTION FACTOR BY GROWTH-HORMONE [J].
CAMPBELL, GS ;
MEYER, DJ ;
RAZ, R ;
LEVY, DE ;
SCHWARTZ, J ;
CARTERSU, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) :3974-3979
[4]   INTEGRINS AND SIGNAL-TRANSDUCTION PATHWAYS - THE ROAD TAKEN [J].
CLARK, EA ;
BRUGGE, JS .
SCIENCE, 1995, 268 (5208) :233-239
[5]  
FINBLOOM DS, 1995, J IMMUNOL, V155, P1079
[6]  
HAMMARSTROM L., 1967, CALCIFIED TISSUE RES, V1, P229, DOI 10.1007/BF02008094
[7]   TRANSCRIPTIONAL REGULATION BY EXTRACELLULAR SIGNALS - MECHANISMS AND SPECIFICITY [J].
HILL, CS ;
TREISMAN, R .
CELL, 1995, 80 (02) :199-211
[8]   JAKS AND STATS IN SIGNALING BY THE CYTOKINE RECEPTOR SUPERFAMILY [J].
IHLE, JN ;
KERR, IM .
TRENDS IN GENETICS, 1995, 11 (02) :69-74
[9]   GENETICS OF SIGNAL-TRANSDUCTION - TALES FROM THE MOUSE [J].
IMAMOTO, A ;
SORIANO, P ;
STEIN, PL .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (01) :40-46
[10]  
JOSEPH BK, 1994, ANAT EMBRYOL, V189, P489