Cherradi Nadia, Lejczak Cyrille, Desroches-Castan Agnes, Feige Jean-Jacques
Institut National de la Santé et de la Recherche Médicale, Equipe Mixte 01-05, Department of Cellular Responses and Dynamics, Commissariat à l'Energie Atomique, F-38054 Grenoble, France.
Mol Endocrinol. 2006 Apr;20(4):916-30. doi: 10.1210/me.2005-0121. Epub 2005 Nov 23.
Expression of vascular endothelial growth factor (VEGF), an endothelial cell-specific mitogen and a potent angiogenic factor, is up-regulated by a variety of factors including hypoxia, growth factors, and hormones. In the adrenal cortex, regulation of VEGF expression by the pituitary hormone ACTH ensures the maintenance of the organ vasculature. We have previously shown that ACTH evokes a rapid and transient increase in VEGF mRNA levels in primary adrenocortical cells through transcription-independent mechanisms. We further demonstrated that the zinc finger RNA-binding protein Tis11b (tetradecanoyl phorbol acetate-inducible-sequence 11b) destabilizes VEGF mRNA through its 3'-untranslated region (3'-UTR) and that Tis11b is involved in the decay phase of ACTH-induced VEGF mRNA expression. In the present study, we attempted to determine the mechanisms underlying ACTH-elicited increase in VEGF mRNA levels in adrenocortical cells. We show that ACTH triggers an increase in the levels of the mRNA-stabilizing protein HuR in the cytoplasm and a concomitant decrease in the levels of HuR in the nucleus. This process is accompanied by an increased association of HuR with the nucleocytoplasmic shuttling protein pp32, indicating that ACTH induces HuR translocation from the nuclear to the cytoplasmic compartment. Leptomycin B, a specific inhibitor of CRM1-dependent nuclear export of pp32, significantly reduced ACTH-induced VEGF mRNA levels. Furthermore, RNA interference-mediated depletion of HuR in adrenocortical cells abrogated ACTH-induced VEGF mRNA expression. Finally, we show that Tis11b and HuR exert antagonistic effects on VEGF 3'-UTR in vitro. Although both proteins could bind simultaneously on VEGF 3'-UTR, Tis11b markedly decreases HuR-binding to this RNA sequence. Altogether, these results suggest that the RNA-stabilizing protein HuR is instrumental to ACTH-induced expression of VEGF mRNA and that the nuclear export of HuR is a rate-limiting step in this process. HuR appears to transiently stabilize VEGF transcripts after ACTH stimulation of adrenocortical cells, and Tis11b appears to subsequently trigger their degradation.
血管内皮生长因子(VEGF)是一种内皮细胞特异性有丝分裂原和强效血管生成因子,其表达受多种因素上调,包括缺氧、生长因子和激素。在肾上腺皮质中,垂体激素促肾上腺皮质激素(ACTH)对VEGF表达的调节确保了器官脉管系统的维持。我们之前已经表明,ACTH通过不依赖转录的机制,引起原代肾上腺皮质细胞中VEGF mRNA水平快速短暂升高。我们进一步证明,锌指RNA结合蛋白Tis11b(十四酰佛波醇乙酸酯诱导序列11b)通过其3'-非翻译区(3'-UTR)使VEGF mRNA不稳定,并且Tis11b参与ACTH诱导的VEGF mRNA表达的衰减阶段。在本研究中,我们试图确定ACTH引起肾上腺皮质细胞中VEGF mRNA水平升高的潜在机制。我们发现,ACTH触发细胞质中mRNA稳定蛋白HuR水平升高,同时细胞核中HuR水平降低。这一过程伴随着HuR与核质穿梭蛋白pp32的结合增加,表明ACTH诱导HuR从细胞核转运到细胞质区室。CRM1依赖性pp32核输出的特异性抑制剂放线菌素B显著降低了ACTH诱导的VEGF mRNA水平。此外,RNA干扰介导的肾上腺皮质细胞中HuR的缺失消除了ACTH诱导的VEGF mRNA表达。最后,我们表明Tis11b和HuR在体外对VEGF 3'-UTR发挥拮抗作用。虽然这两种蛋白可以同时结合在VEGF 3'-UTR上,但Tis11b显著降低HuR与该RNA序列的结合。总之,这些结果表明,RNA稳定蛋白HuR对ACTH诱导的VEGF mRNA表达起作用,并且HuR的核输出是这一过程中的限速步骤。在ACTH刺激肾上腺皮质细胞后,HuR似乎短暂稳定VEGF转录本,随后Tis11b似乎触发其降解。