DARPP-32 and CREB are present in type 2 iodothyronine deiodinase-producing tanycytes:: implications for the regulation of type 2 deiodinase activity

被引:31
作者
Fekete, C
Mihály, E
Herscovici, S
Salas, J
Tu, H
Larsen, PR
Lechan, RM
机构
[1] Tufts Univ New England Med Ctr, Tupper Res Inst, Boston, MA 02111 USA
[2] Tufts Univ New England Med Ctr, Dept Med, Div Endocrinol Diabet Metab & Mol Med, Boston, MA 02111 USA
[3] Hungarian Acad Sci, Inst Expt Med, Dept Neurobiol, H-1083 Budapest, Hungary
[4] Brigham & Womens Hosp, Dept Med, Div Thyroid, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Boston, MA 02115 USA
[6] Tufts Univ, Sch Med, Dept Neurosci, Boston, MA 02111 USA
关键词
type 2 iodothyronine deiodinase; DARPP-32; CREB; tanycyte;
D O I
10.1016/S0006-8993(00)02105-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Type 2 iodothyronine deiodinase, an enzyme involved in the conversion of thyroxin to the biologically active 3,5,3'-triiodothyronine, is highly concentrated in a group of specialized ependymal cells, tanycytes, lining the wall and floor of the third ventricle. As this distribution is highly reminiscent of the distribution of cells containing the phosphatase inhibitor, DARPP-32, we raised the possibility that these two proteins may coexist in tanycytes and that DARPP-32 may modulate type 2 deiodinase activity by regulating the phosphorylation state of the cAMP regulatory factor, CREB. To address this question, double-labeling histochemical studies were performed for type 2 deiodinase mRNA and DARPP-32 immunoreactivity (IR), or DARPP-32- and CREB-IR in the same tissue sections. Type 2 deiodinase mRNA was found in the cell bodies of all DARPP-32-immunolabeled tanycytes. Both type 2 deiodinase mRNA and DARPP-32-IR also extended into tanycyte processes that ramified in the arcuate nucleus and median eminence, in close association with blood vessels and portal capillaries. In contrast, type 2 deiodinase mRNA was not present in the same cells that contained DARPP-32-IR in the pituitary gland. All tanycytes containing DARPP-32-IR also contained CREB-IR in their nucleus. Since type 2 deiodinase activity can be induced by substances that increase cAMP, we hypothesize that DARPP-32 may regulate the activity of type 2 deiodinase by prolonging the activation of CREB. Selectivity for the colocalization of these factors to tanycytes but not the pituitary gland, may explain the heterogeneous response of type 2 deiodinase activity in these two loci in response to specific stimuli such as fasting. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:154 / 161
页数:8
相关论文
共 49 条
[1]   INCREASED DOPAMINERGIC ACTIVITY INHIBITS BASAL AND METOCLOPRAMIDE-STIMULATED PROLACTIN AND THYROTROPIN SECRETION [J].
AGNER, T ;
HAGEN, C ;
ANDERSEN, AN ;
DJURSING, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 62 (04) :778-782
[2]   ULTRASTRUCTURAL IDENTIFICATION OF CATECHOLAMINE NEURONS IN HYPOTHALAMIC PERIVENTRICULAR-ARCUATE NUCLEUS-MEDIAN EMINENCE COMPLEX WITH SPECIAL REFERENCE TO QUANTITATIVE ASPECTS [J].
AJIKA, K ;
HOKFELT, T .
BRAIN RESEARCH, 1973, 57 (01) :97-117
[3]   Characterization of the 5′-flanking and 5′-untranslated regions of the cyclic adenosine 3′,5′-monophosphate-responsive human type 2 iodothyronine deiodinase gene [J].
Bartha, T ;
Kim, SW ;
Salvatore, D ;
Gereben, B ;
Tu, HM ;
Harney, JW ;
Rudas, P ;
Larsen, PR .
ENDOCRINOLOGY, 2000, 141 (01) :229-237
[4]  
CARD JP, 1978, AM J ANAT, V151, P173, DOI 10.1002/aja.1001510203
[5]   EFFECT OF LOW-DOSE DOPAMINE INFUSION ON BASAL AND STIMULATED TSH AND PROLACTIN CONCENTRATIONS IN MAN [J].
CONNELL, JMC ;
BALL, SG ;
BALMFORTH, AJ ;
BEASTALL, GH ;
DAVIES, DL .
CLINICAL ENDOCRINOLOGY, 1985, 23 (02) :185-192
[6]   EXPRESSION OF THYROID-HORMONE RECEPTOR BETA-2 IN RAT HYPOTHALAMUS [J].
COOK, CB ;
KAKUCSKA, I ;
LECHAN, RM ;
KOENIG, RJ .
ENDOCRINOLOGY, 1992, 130 (02) :1077-1079
[7]   INDUCTION OF TYPE-II 5'-DEIODINASE ACTIVITY BY CYCLIC ADENOSINE 3', 5'-MONOPHOSPHATE IN CULTURED RAT ASTROGLIAL CELLS [J].
COURTIN, F ;
CHANTOUX, F ;
PIERRE, M ;
FRANCON, J .
ENDOCRINOLOGY, 1988, 123 (03) :1577-1581
[8]   AN ANALYSIS OF THE SOURCES AND QUANTITY OF 3,5,3'-TRIIODOTHYRONINE SPECIFICALLY BOUND TO NUCLEAR RECEPTORS IN RAT CEREBRAL-CORTEX AND CEREBELLUM [J].
CRANTZ, FR ;
SILVA, JE ;
LARSEN, PR .
ENDOCRINOLOGY, 1982, 110 (02) :367-375
[9]   Fasting-induced increase in type II iodothyronine deiodinase activity and messenger ribonucleic acid levels is not reversed by thyroxine in the rat hypothalamus [J].
Diano, S ;
Naftolin, F ;
Goglia, F ;
Horvath, TL .
ENDOCRINOLOGY, 1998, 139 (06) :2879-2884
[10]   TRIIODOTHYRONINE EXERTS DIRECT CELL-SPECIFIC REGULATION OF THYROTROPIN-RELEASING-HORMONE GENE-EXPRESSION IN THE HYPOTHALAMIC PARAVENTRICULAR NUCLEUS [J].
DYESS, EM ;
SEGERSON, TP ;
LIPOSITS, Z ;
PAULL, WK ;
KAPLAN, MM ;
WU, P ;
JACKSON, IMD ;
LECHAN, RM .
ENDOCRINOLOGY, 1988, 123 (05) :2291-2297