Lee M M, Sato-Bigbee C, De Vries G H
Department of Cell Biology, Neurobiology, and Anatomy, Loyola University Medical Center, Maywood, Illinois, USA.
J Neurosci Res. 1996 Oct 15;46(2):204-10. doi: 10.1002/(SICI)1097-4547(19961015)46:2<204::AID-JNR8>3.0.CO;2-L.
Both axolemma-enriched fractions (AEF) and cyclic AMP have been shown to regulate the proliferation and differentiation of cultured primary Schwann cells (SC). We have evaluated the role of CREB, a transcription factor that binds to the cAMP-responsive element, in mediating the AEF-stimulated SC proliferation and differentiation. We detected CREB in nuclear extracts derived from SC stimulated with 40 micrograms/ml of AEF for 16, 24, 48, 72, and 96 hr, using a DNA-electrophoretic mobility shift assay. Unstimulated quiescent SC contained low levels of CREB which increased to a maximal level after 48 hr of AEF treatment. Using anti-CREB antibodies and Western blot analysis, after 24 hr of AEF treatment we first detected CREB as a 45 kDa protein which reached a maximal level of expression after 72 hr. Double labeled immunocytochemistry using anti-CREB and anti-5-bromo-2'-deoxy-uridine antibodies demonstrated maximal CREB expression after 72 hr of AEF treatment, closely coinciding with the temporal expression of SC proliferation. At all times examined, all AEF-treated SC labeled by anti-CREB antibodies were also labeled with anti-BrdU antibodies. These observations are consistent with the view that CREB could play an important role in the induction of SC proliferation by AEF.
富含轴膜的组分(AEF)和环磷酸腺苷(cAMP)均已被证明可调节培养的原代雪旺细胞(SC)的增殖和分化。我们评估了与cAMP反应元件结合的转录因子CREB在介导AEF刺激的SC增殖和分化中的作用。我们使用DNA电泳迁移率变动分析,在来自用40微克/毫升AEF刺激16、24、48、72和96小时的SC的核提取物中检测到了CREB。未受刺激的静止SC含有低水平的CREB,在AEF处理48小时后增加到最大水平。使用抗CREB抗体和蛋白质免疫印迹分析,在AEF处理24小时后,我们首次检测到CREB为一种45 kDa的蛋白质,其在72小时后达到最大表达水平。使用抗CREB和抗5-溴-2'-脱氧尿苷抗体的双重标记免疫细胞化学显示,在AEF处理72小时后CREB表达最高,这与SC增殖的时间表达密切一致。在所有检测时间点,所有用抗CREB抗体标记的AEF处理的SC也都用抗BrdU抗体标记。这些观察结果与CREB可能在AEF诱导SC增殖中起重要作用的观点一致。