Nitric oxide synthase expression in bone cells

被引:83
作者
Fox, SW [1 ]
Chow, JWM [1 ]
机构
[1] Univ London St Georges Hosp, Sch Med, Dept Histopathol, London SW17 0RE, England
基金
英国惠康基金;
关键词
nitric oxide synthase; immunohistochemistry; bone; osteoblasts; inflammation;
D O I
10.1016/S8756-3282(98)00070-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have localized the expression of the three main nitric oxide synthases (eNOS, bNOS, and iNOS) in bone cells of rats and humans using immunohistochemistry. The predominant isoform expressed in normal adult bone was the constitutive isoform, eNOS, mainly in cells of osteoblastic lineage, In adult bone, the osteoblast lineage cells exhibiting eNOS expression were flat bone lining cells and osteocytes, but cuboidal osteoblasts were consistently negative. Expression for bNOS was not detected in any bone cells. iNOS expression was not detected in any cells of osteoblastic lineage in normal adult rat or human bone, but was observed in cuboidal osteoblasts of adult rats with experimental colitis, in which the suppression in bone formation may be cytokine mediated. Osteoclasts in normal rat tissue showed expression for both eNOS and iNOS, but these were patchy. As for cells of the osteoblast lineage, osteoclasts were negative for bNOS, Thus, our findings support evidence, from in vitro studies and from animal experiments, that nitric oxide may play an important role in the physiology of bone. (Bone 23:1-6; 1998) (C) 1998 by Elsevier Science Inc All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 29 条
[1]   Regulation of endothelial nitric-oxide synthase during hypoxia [J].
Arnet, UA ;
McMillan, A ;
Dinerman, JL ;
Ballermann, B ;
Lowenstein, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (25) :15069-15073
[2]  
BAYLIS SA, 1994, INT C BIOCH MOL BIOL, P66
[3]   BIDIRECTIONAL REGULATION OF OSTEOCLAST FUNCTION BY NITRIC-OXIDE SYNTHASE ISOFORMS [J].
BRANDI, ML ;
HUKKANEN, M ;
UMEDA, T ;
MORADIBIDHENDI, N ;
BIANCHI, S ;
GROSS, SS ;
POLAK, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2954-2958
[4]   CANDIDATES FOR THE MECHANOSENSORY SYSTEM IN BONE [J].
COWIN, SC ;
MOSSSALENTIJN, L ;
MOSS, ML .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1991, 113 (02) :191-197
[5]   CYTOKINES INDUCE NITRIC-OXIDE PRODUCTION IN MOUSE OSTEOBLASTS [J].
DAMOULIS, PD ;
HAUSCHKA, PV .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 201 (02) :924-931
[6]  
Evans DM, 1996, J BONE MINER RES, V11, P300
[7]   Nitric oxide is an early mediator of the increase in bone formation by mechanical stimulation [J].
Fox, SW ;
Chambers, TJ ;
Chow, JWM .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1996, 270 (06) :E955-E960
[8]  
FRANGOS JA, 1995, FASEB J, V9, pA673
[9]   Expression of nitric oxide synthase isoforms in bone and bone cell cultures [J].
Helfrich, MH ;
Evans, DE ;
Grabowski, PS ;
Pollock, JS ;
Ohshima, H ;
Ralston, SH .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (07) :1108-1115
[10]   CYTOKINE-STIMULATED EXPRESSION OF INDUCIBLE NITRIC-OXIDE SYNTHASE BY MOUSE, RAT, AND HUMAN OSTEOBLAST-LIKE CELLS AND ITS FUNCTIONAL-ROLE IN OSTEOBLAST METABOLIC-ACTIVITY [J].
HUKKANEN, M ;
HUGHES, FJ ;
BUTTERY, LDK ;
GROSS, SS ;
EVANS, TJ ;
SEDDON, S ;
RIVEROSMORENO, V ;
MACINTYRE, I ;
POLAK, JM .
ENDOCRINOLOGY, 1995, 136 (12) :5445-5453