GENE-EXPRESSION IN THE DEVELOPING CEREBELLUM DURING PERINATAL HYPOTHYROIDISM AND HYPERTHYROIDISM

被引:57
作者
FIGUEIREDO, BC
ALMAZAN, G
MA, Y
TETZLAFF, W
MILLER, FD
CUELLO, AC
机构
[1] MCGILL UNIV, DEPT PHARMACOL & THERAPEUT, 3655 DRUMMOND ST, ROOM 1325, MONTREAL H3G 1Y6, QUEBEC, CANADA
[2] UNIV ALBERTA, DEPT ANAT & CELL BIOL, EDMONTON T6G 2E1, ALBERTA, CANADA
[3] UNIV CALGARY, DEPT ANAT & CELL BIOL, CALGARY T2N 1N4, ALBERTA, CANADA
来源
MOLECULAR BRAIN RESEARCH | 1993年 / 17卷 / 3-4期
基金
英国医学研究理事会;
关键词
P75NGFR; LOW-AFFINITY NERVE GROWTH FACTOR RECEPTOR; GAP-43; GROWTH-ASSOCIATED PROTEIN-43; T-ALPHA-1; ALPHA-TUBULIN; MYELIN BASIC PROTEIN; MYELIN PROTEOLIPID PROTEIN;
D O I
10.1016/0169-328X(93)90010-M
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The intensity of p75NGFR receptor-like immunoreactivity and the mRNAs encoding p75NGFR, Talpha1 alpha-tubulin, GAP-43 and the myelin proteins MBP and PLP were measured in the developing cerebellum to study the effects of perinatal thyroid hormone imbalance in rats. Results compared to age-matched controls provide in vivo evidence for differential gene regulation by thyroid hormone in the developing cerebellum. We found that p75NGFR immunoreactivity was strikingly elevated in hypothyroid rats, whereas p75NGFR mRNA content remained only twice as high as that of control levels on postnatal day 15 (P15). When p75NGFR immunoreactivity was still elevated in hypothyroid rats, Purkinje cells exhibited proximal axonal varicosities, axonal twisting and differences in axonal caliber. The mRNAs encoding proteins involved with neurite growth-promoting elements, Talpha1 alpha-tubulin and GAP-43, were also increased in hypothyroidism, possibly reflecting a neuronal response to a deficiency in, or damage to, cerebellar neurons, or a general delay in their down regulation. Similar increases were not observed for the myelin specific genes. MBP and PLP mRNAs were first detected on P2 of hyperthyroid rats, and they increased with age. Hypo- or hyperthyroidism did not affect the initial onset of MBP and PLP expression, however, hyperthyroidism increased levels of PLP and MBP mRNAs between P2 and P10. By contrast, the most consistent decrease in MBP and PLP mRNAs in rats with thyroid hormone deficiency was observed only on P10. At later times (P15 and P30), the two mRNA levels were similar to controls in all groups. These results are consistent with a role for thyroid hormone in the earlier stages of cerebellar myelination. Hypothyroidism led to specific increases in Talpha1 alpha-tubulin and GAP-43 mRNAs, and in the immunoreactivity and mRNA levels of p75NGFR receptor - all changes that may play a role in the observed abnormal neuronal outgrowth.
引用
收藏
页码:258 / 268
页数:11
相关论文
共 71 条
[1]  
ALEXANDER KA, 1987, J BIOL CHEM, V262, P6108
[2]   TRIIODOTHYRONINE STIMULATION OF OLIGODENDROGLIAL DIFFERENTIATION AND MYELINATION - A DEVELOPMENTAL-STUDY [J].
ALMAZAN, G ;
HONEGGER, P ;
MATTHIEU, JM .
DEVELOPMENTAL NEUROSCIENCE, 1985, 7 (01) :45-54
[3]   PRENATAL DEVELOPMENT OF CEREBELLAR SYSTEM IN RAT .1. CYTOGENESIS AND HISTOGENESIS OF DEEP NUCLEI AND CORTEX OF CEREBELLUM [J].
ALTMAN, J ;
BAYER, SA .
JOURNAL OF COMPARATIVE NEUROLOGY, 1978, 179 (01) :23-48
[5]   REGULATION OF MYELIN BASIC-PROTEIN (ARGININE) METHYLTRANSFERASE BY THYROID-HORMONE IN MYELINOGENIC CULTURES OF CELLS DISSOCIATED FROM EMBRYONIC MOUSE-BRAIN [J].
AMUR, SG ;
SHANKER, G ;
PIERINGER, RA .
JOURNAL OF NEUROCHEMISTRY, 1984, 43 (02) :494-498
[6]   REGULATION OF 5 TUBULIN ISOTYPES BY THYROID-HORMONE DURING BRAIN-DEVELOPMENT [J].
ANIELLO, F ;
COUCHIE, D ;
GRIPOIS, D ;
NUNEZ, J .
JOURNAL OF NEUROCHEMISTRY, 1991, 57 (05) :1781-1786
[7]   SPLICING OF JUVENILE AND ADULT TAU-MESSENGER RNA VARIANTS IS REGULATED BY THYROID-HORMONE [J].
ANIELLO, F ;
COUCHIE, D ;
BRIDOUX, AM ;
GRIPOIS, D ;
NUNEZ, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :4035-4039
[8]   ACCUMULATION OF 4 MYELIN BASIC-PROTEINS IN MOUSE-BRAIN DURING DEVELOPMENT [J].
BARBARESE, E ;
CARSON, JH ;
BRAUN, PE .
JOURNAL OF NEUROCHEMISTRY, 1978, 31 (04) :779-782
[9]   PRIMARY STRUCTURE AND TRANSCRIPTIONAL REGULATION OF GAP-43, A PROTEIN ASSOCIATED WITH NERVE GROWTH [J].
BASI, GS ;
JACOBSON, RD ;
VIRAG, I ;
SCHILLING, J ;
SKENE, JHP .
CELL, 1987, 49 (06) :785-791
[10]  
BENOWITZ LI, 1983, J NEUROSCI, V3, P2153