Thyroid hormone induces protein secretion and morphological changes in astroglial cells with an increase in expression of glial fibrillary acidic protein

1997 ◽  
Vol 154 (1) ◽  
pp. 167-175 ◽  
Author(s):  
F R S Lima ◽  
A G Trentin ◽  
D Rosenthal ◽  
C Chagas ◽  
V Moura Neto

Abstract Thyroid hormone (T3) induces in vitro differentiation of astrocytes from the developing rat brain. T3 treatment induced the appearance of long processes in cultured cerebral hemisphere and mesencephalon astrocytes from embryonic and newborn rats. T3 treatment also produced a change in the morphology of cultured cerebellar astrocytes from 10-day-old rats, but not in cerebellar astrocytes from newborn rats. An increased expression of glial fibrillary acidic protein (GFAP) was also seen in the T3-treated newborn cerebral hemisphere and mesencephalic astrocytes. The morphological changes were induced earlier when the astrocytes were treated with conditioned medium (CM) obtained from cultures previously exposed to T3. Our results show that astrocytes from the developing rat brain are not homogenous in their responsiveness to T3. Furthermore, the fact that CM produces a response similar to that obtained with T3 treatment but in less time, suggests that T3 might induce the secretion of factors by cultured astrocytes. These factors might, by an autocrine/paracrine effect, induce the expression of GFAP and differentiation in developing brain astrocytes. Journal of Endocrinology (1997) 154, 167–175

1996 ◽  
Vol 139 (1) ◽  
pp. 84-93 ◽  
Author(s):  
G.Jean Harry ◽  
Tamara J. Schmitt ◽  
Zhaolong Gong ◽  
Hayes Brown ◽  
Nasser Zawia ◽  
...  

2004 ◽  
Vol 24 (2) ◽  
pp. 136-143 ◽  
Author(s):  
Hui-Min Yu ◽  
Tian-Ming Yuan ◽  
Wei-Zhong Gu ◽  
Jian-Ping Li

1980 ◽  
Vol 199 (2) ◽  
pp. 493-500 ◽  
Author(s):  
P.E. Stieg ◽  
H.K. Kimelberg ◽  
J.E. Mazurkiewicz ◽  
G.A. Banker

Glia ◽  
1992 ◽  
Vol 6 (3) ◽  
pp. 180-187 ◽  
Author(s):  
Ignacio Torres-Aleman ◽  
Maria Teresa Rejas ◽  
Sebastian Pons ◽  
Luis Miguel Garcia-Segura

Endocrinology ◽  
2004 ◽  
Vol 145 (11) ◽  
pp. 5013-5020 ◽  
Author(s):  
Christopher M. Schoonover ◽  
Melissa M. Seibel ◽  
Dawn M. Jolson ◽  
Mary Jo Stack ◽  
Rounak J. Rahman ◽  
...  

Abstract Thyroid hormone (TH) is necessary for normal axonal myelination. Myelin basic protein (MBP) is a structural protein essential for myelin function. In this study, we demonstrate that perinatal hypothyroidism regulates MBP mRNA levels via indirect mechanisms. We observed decreased MBP mRNA accumulation in the hypothyroid rat brain at postnatal (PN) d 10 and 50. Acute TH replacement did not rescue hypothyroid MBP mRNA levels at PN5, 10, or 50. TH is necessary for normal intrahemispheric commissure development including the anterior commissure (AC) and the corpus callosum (CC). We determined that perinatal hypothyroidism decreases AC area and cellularity in the developing rat brain by PN10 and 50. In the developing CC, hypothyroidism initially increases area and cellularity by PN5, but then ultimately decreases area and cellularity by PN50. MBP-expressing oligodendrocytes are a recognized target of TH and are responsible for myelination within intrahemispheric commissures. We found that hypothyroidism reduces the number of mature oligodendrocytes within both the AC and CC. This reduction is noted at PN5, 10, and 50 in the AC and by PN10 and 50 in the CC. Together, these data suggest that TH regulates MBP mRNA levels through indirect mechanisms. These data demonstrate the complex mechanisms whereby TH regulates myelination in the developing brain.


1994 ◽  
Vol 111 (4) ◽  
pp. 997-1002 ◽  
Author(s):  
Gabriel Olmos ◽  
Regina Alemany ◽  
Pablo V. Escriba ◽  
Jesús A. García-Sevilla

Glia ◽  
1991 ◽  
Vol 4 (3) ◽  
pp. 276-284 ◽  
Author(s):  
Catherine Faivre-Sarrailh ◽  
Abdelhaq Rami ◽  
Christiane Fages ◽  
Marcienne Tardy

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