CREB modulates calcium signaling in cAMP-induced bone marrow stromal cells (BMSCs)

• BMSCs but not fibroblasts are responsive to dopamine and KCl.
• Silencing of CREB reduces the number of dopamine and KCl responsive cells in cAMP induced BMSCs.
• Knock-down of CREB activity minimally affect calcium signaling in BMSCs without cAMP treatment.
• Knock-down of CREB activity greatly reduces calcium signaling in cAMP-induced BMSCs.
• CREB alters expression of certain dopamine receptors.

Calcium signaling has a versatile role in many important cellular functions. Despite its importance, regulation of calcium signaling in bone marrow stromal cells (BMSCs, also known as bone marrow-derived mesenchymal stem cells) has not been explored extensively. Our previous study revealed that cyclic adenosine monophosphate (cAMP) enabled BMSCs to generate calcium signal upon stimulation by dopamine, KCl and glutamate. Concurrently, cAMP transiently activated the transcription factor cAMP response element binding protein (CREB) in BMSCs. Activity of CREB can be modulated by the calcium/calmodulin-dependent kinase signaling pathway, however, whether the calcium signaling observed in cAMP-induced BMSCs requires CREB has not been investigated. In an effort to uncover the role of CREB in the generation of calcium signaling in response to modulators such as dopamine and KCl, we knocked down CREB activity in BMSCs. Our study indicated that BMSCs, but not its close relative fibroblasts, are responsive to dopamine and KCl after cAMP treatment. Calcium signal elicited by dopamine depends, in part, on calcium influx whereas that elicited by KCl depends completely on calcium influx. Knock-down of CREB activity significantly reduced or abolished the cAMP-induced calcium response, and reintroducing a constitutively active CREB partially restored the calcium response.

Figure optionsDownload as PowerPoint slide