The neuropeptide calcitonin gene-related peptide inhibits TNF-α but poorly induces IL-6 production by fetal rat osteoblasts

被引:31
作者
Millet, I [1 ]
Vignery, A [1 ]
机构
[1] Yale Univ, Sch Med, Dept Orthopaed & Rehabil, New Haven, CT 06510 USA
关键词
osteoblasts; CGRP; TNF-alpha; IL-6; cAMP;
D O I
10.1006/cyto.1997.0245
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
Tumour necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6) are potent inflammatory cytokines produced by osteoblasts and whose contribution to bone loss occurring in oestrogen deficiency is well documented, Calcitonin gene-related peptide (CC;RP) is a neuropeptide abundantly concentrated in sensory nerve endings innervating bone metaphyses and periosteum suggesting that it controls bone homeostasis locally, Since CGRP was shown to inhibit TNF-alpha production by T cells and stimulate IL-6 expression by fibroblasts, this study was designed to investigate whether CGRP regulated TNF-alpha and IL-6 production by osteoblasts. We show that CGRP inhibits the production of TNF-alpha by both lipopolysaccharide (LPS)-and LL-l-stimulated fetal rat osteoblasts. Like CGRP, the cAMP agonists prostaglandin E-2 (PGE(2)), dibutyryl cAMP (Bt(2)cAMP) and forskolin inhibit TNF-alpha production by osteoblasts. Exposure of osteoblasts to a high dose of phorbol myristoyl acetate (PMA) to deplete PKC activity abolished CGRP-mediated TNF-alpha suppression, In contrast with its potent inhibition of TNP-alpha production, we show that CGRP is a weak inducer of IL-6 when compared to PGE(2), Bt(2)cAMP and forskolin, However, in presence of isobutylmethylxanthine (IBMX) CGRP stimulates the production of IL-6, Collectively, these data suggest that the inhibition of TNF-alpha by CGRP is cAMP dependent and PMA sensitive and that the concentration of intracellular cAMP may be a regulatory mechanism for IL-6 gene expression in osteoblasts. (C) 1997 Academic Press Limited.
引用
收藏
页码:999 / 1007
页数:9
相关论文
共 66 条
[1]   A cDNA encoding the calcitonin gene-related peptide type 1 receptor [J].
Aiyar, N ;
Rand, K ;
Elshourbagy, NA ;
Zeng, ZZ ;
Adamou, JE ;
Bergsma, DJ ;
Li, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (19) :11325-11329
[2]  
AMMANN P, 1995, J BONE MINER RES S1, V10
[3]   THE OSTEOGENIC STIMULATING EFFECT OF NEUROACTIVE CALCITONIN GENE-RELATED PEPTIDE [J].
BERNARD, GW ;
SHIH, C .
PEPTIDES, 1990, 11 (04) :625-632
[4]   STIMULATION OF BONE-RESORPTION AND INHIBITION OF BONE-FORMATION INVITRO BY HUMAN-TUMOR NECROSIS FACTORS [J].
BERTOLINI, DR ;
NEDWIN, GE ;
BRINGMAN, TS ;
SMITH, DD ;
MUNDY, GR .
NATURE, 1986, 319 (6053) :516-518
[5]   CONTROL OF CACHECTIN (TUMOR-NECROSIS-FACTOR) SYNTHESIS - MECHANISMS OF ENDOTOXIN RESISTANCE [J].
BEUTLER, B ;
KROCHIN, N ;
MILSARK, IW ;
LUEDKE, C ;
CERAMI, A .
SCIENCE, 1986, 232 (4753) :977-980
[6]   PROSTAGLANDIN-E(2) RAPIDLY STIMULATES INSULIN-LIKE GROWTH FACTOR-I GENE-EXPRESSION IN PRIMARY RAT OSTEOBLAST CULTURES - EVIDENCE FOR TRANSCRIPTIONAL CONTROL [J].
BICHELL, DP ;
ROTWEIN, P ;
MCCARTHY, TL .
ENDOCRINOLOGY, 1993, 133 (03) :1020-1028
[7]   EFFECTS OF TUMOR-NECROSIS-FACTOR ON BONE-FORMATION INVITRO [J].
CANALIS, E .
ENDOCRINOLOGY, 1987, 121 (05) :1596-1604
[8]   PRODUCTION OF VARIOUS CYTOKINES BY NORMAL HUMAN OSTEOBLAST-LIKE CELLS IN RESPONSE TO INTERLEUKIN-1-BETA AND TUMOR-NECROSIS-FACTOR-ALPHA - LACK OF REGULATION BY 17-BETA-ESTRADIOL [J].
CHAUDHARY, LR ;
SPELSBERG, TC ;
RIGGS, BL .
ENDOCRINOLOGY, 1992, 130 (05) :2528-2534
[9]   CALCITONIN GENE-RELATED PEPTIDE STIMULATES INTRACELLULAR CAMP VIA A PROTEIN KINASE-C-CONTROLLED MECHANISM IN HUMAN OCULAR CILIARY EPITHELIAL-CELLS [J].
CROOK, RB ;
YABU, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 188 (02) :662-670
[10]   HUMAN SYNTHETIC CALCITONIN GENE-RELATED PEPTIDE INHIBITS BONE-RESORPTION INVITRO [J].
DSOUZA, SM ;
MACINTYRE, I ;
GIRGIS, SI ;
MUNDY, GR .
ENDOCRINOLOGY, 1986, 119 (01) :58-61