Retinoic acid receptors beta and gamma distinguish retinoid signals for growth inhibition and neuritogenesis in human neuroblastoma cells

被引:24
作者
Cheung, B
Hocker, JE
Smith, SA
Reichert, U
Norris, MD
Haber, M
Stewart, BW
Marshall, GM
机构
[1] SYDNEY CHILDRENS HOSP,CHILDRENS CANC RES INST,RANDWICK,NSW 2031,AUSTRALIA
[2] CTR INT RECH DERMATOL GALDERMA,F-06902 VALBONNE,FRANCE
基金
英国医学研究理事会;
关键词
D O I
10.1006/bbrc.1996.1804
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
Retinoids induce marked growth inhibition and neuritic differentiation in human neuroblastoma cells. Expression patterns of nuclear retinoic acid receptors (RAR) in embryonic and adult tissues suggests that RAR subtypes alpha, beta and gamma have tissue-specific functions. We have transfected a human neuroblastoma tumor cell line with a vector expressing either human RAR alpha, beta or gamma cDNAs. In the absence of exogenous retinoid, RAR beta transfectants demonstrated marked growth inhibition without morphologic evidence of differentiation, whereas transfectant clones overexpressing RARs alpha and gamma had no significant reduction in cell growth rates. Although RAR gamma transfectants were sensitive to the growth inhibitory effects of exogenous retinoids, these cells demonstrated resistance to the neuritogenic retinoid effects. Only RAR beta transfectants exhibited increased sensitivity to retinoids added in vitro. These results suggest that distinct neuritogenic and growth inhibitory signalling pathways exist in neuroblastoma cells and that RAR beta expression may be necessary for the retinoid growth inhibitory pathway. (C) 1996 Academic Press, Inc.
引用
收藏
页码:349 / 354
页数:6
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