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视黄酸诱导星形胶质细胞中III型脱碘酶活性

Induction of type III-deiodinase activity in astroglial cells by retinoids.

作者信息

Esfandiari A, Gagelin C, Gavaret J M, Pavelka S, Lennon A M, Pierre M, Courtin F

机构信息

U. 96 INSERM, Unité de Recherche sur la Glande Thyroîde et la Régulation Hormonale, Le Kremlin-Bicêtre, France.

出版信息

Glia. 1994 Jul;11(3):255-61. doi: 10.1002/glia.440110306.

DOI:10.1002/glia.440110306
PMID:7525478
Abstract

Thyroid hormones and retinoic acid (RA) are important modulators of growth, development, and differentiation. Type III deiodinase (D-III), which catalyzes thyroid hormones degradation in the brain and in cultured astroglial cells, is induced in astroglial cells by multiple pathways, including cAMP, 12.0-tetradecanoylphorbol-13-acetate (TPA), fibroblast growth factors, and thyroid hormones themselves. In the present study, the effects of retinoids on D-III activity were examined in astroglial cells cultures in a chemically defined medium devoid of hormones and growth factors. Incubation of astroglial cells with 5 microM all-trans-RA caused up to 200-fold increase in D-III activity, which reached a plateau after 48 h. The retinoid-induced increase in D-III activity was concentration dependent (0.5 microM all-trans-RA and 9-cis-RA producing half-maximal effect). Retinol was effective at physiological concentrations (1 and 10 microM). The 48 h effects of 5 microM all-trans-RA and 10 nM thyroid hormones on D-III activity were at least additive. Addition of 2 nM acidic fibroblast growth factor or 1 mM 8-bromo-cAMP for the last 8 h of a 48 h incubation with 5 microM all-trans-RA did not alter the induction by all-trans-RA, whereas 0.1 microM TPA in the same conditions produced an additive effect with all-trans-RA. All-trans-RA (5 microM) had little or no effect on type II deiodinase, the enzyme which catalyzes the activation of thyroxine to 3,5,3'-triiodothyronine.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

甲状腺激素和视黄酸(RA)是生长、发育和分化的重要调节因子。III型脱碘酶(D-III)催化甲状腺激素在脑和培养的星形胶质细胞中的降解,它在星形胶质细胞中可通过多种途径被诱导,包括环磷酸腺苷(cAMP)、12-十四烷酰佛波醇-13-乙酸酯(TPA)、成纤维细胞生长因子以及甲状腺激素本身。在本研究中,在不含激素和生长因子的化学限定培养基中,检测了视黄酸对视黄醛脱氢酶活性在星形胶质细胞培养物中的影响。用5微摩尔全反式视黄酸孵育星形胶质细胞导致视黄醛脱氢酶活性增加高达200倍,48小时后达到平台期。视黄酸诱导的视黄醛脱氢酶活性增加呈浓度依赖性(0.5微摩尔全反式视黄酸和9-顺式视黄酸产生半数最大效应)。视黄醇在生理浓度(1和10微摩尔)时有效。5微摩尔全反式视黄酸和10纳摩尔甲状腺激素对视黄醛脱氢酶活性的48小时效应至少是相加的。在与5微摩尔全反式视黄酸孵育48小时的最后8小时加入2纳摩尔酸性成纤维细胞生长因子或1毫摩尔8-溴环磷酸腺苷,并不改变全反式视黄酸的诱导作用,而在相同条件下0.1微摩尔TPA与全反式视黄酸产生相加效应。5微摩尔全反式视黄酸对II型脱碘酶几乎没有影响,II型脱碘酶是催化甲状腺素激活为3,5,3'-三碘甲腺原氨酸的酶。(摘要截短至250字)

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