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Rapid effects of triiodothyronine on immediate‐early gene expression in Schwann cells
Author(s) -
Mercier Gilles,
Turque Nathalie,
Schumacher Michael
Publication year - 2001
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.1073
Subject(s) - biology , junb , schwann cell , creb , microbiology and biotechnology , gene expression , immediate early gene , cell culture , ap 1 transcription factor , transcription factor , gene , genetics
In the peripheral nervous system, triiodothyronine (T3) plays an important role in the development and regeneration of nerve fibers and in myelin formation. However, the target genes of T3 in peripheral nerves remain to be identified. We investigated whether T3 activated genes of transcription factors in Schwann cells. Expression of egr‐1 ( krox‐24 ), egr‐2 ( krox‐20 ), egr‐3 , c‐ jun , jun B, c‐ fos , fos B, fra ‐1, fra‐2 , and CREB genes was analyzed by reverse transcription‐polymerase chain reaction (RT‐PCR) in Schwann cells isolated from neonatal rat sciatic nerves and in the cell lines MSC‐80 (mouse Schwann cells), NIH‐3T3 (mouse fibroblasts), and CHO (Chinese hamster ovary cells). Some of these transcription factors have been shown to be involved in Schwann cell differentiation. T3 triggered a rapid (15–30 min), transient (1–2‐h) and strong (6‐ to 15‐fold) stimulation of Egr‐1, Egr‐2, Egr‐3, Jun B, c‐Fos, and Fos B mRNA expression in Schwann cells. In contrast, expression of c‐Jun, Fra‐1, Fra‐2, and CREB mRNA was not affected by T3. The stimulatory effects of T3 could be abolished by adding actinomycin D. T3 triggered the same pattern of gene stimulation in the mouse Schwann cell line MSC80, but not in the NIH‐3T3 and CHO cell lines. Serum activated all the genes that responded to T3 and in addition fra ‐1 and fra ‐2, but not c‐ jun and CREB . Immunoblotting showed that the increase in Egr‐1 and c‐Fos mRNA levels was accompanied by an increase in the corresponding proteins. In addition, shifts of the protein bands indicated a posttranslational modification of the two proteins. These effects of T3 are likely to be mediated by the intracellular T3 receptor, as the D ‐isomer RT3 and T0, which do not bind to T3 receptors, proved ineffective. The present data suggested that T3 may regulate Schwann cell functions and differentiation by transiently activating the expression of specific transcription factors. GLIA 35:81–89, 2001. © 2001 Wiley‐Liss, Inc.