Hoogduijn_2009_Stem.Cells.Dev_18_103

Reference

Title : Functional nicotinic and muscarinic receptors on mesenchymal stem cells - Hoogduijn_2009_Stem.Cells.Dev_18_103
Author(s) : Hoogduijn MJ , Cheng A , Genever PG
Ref : Stem Cells Dev , 18 :103 , 2009
Abstract :

Mesenchymal stem cells (MSCs) are under the control of a large number of signaling systems. In this study, the presence and functionality of the acetylcholine (ACh) signaling system in MSCs was examined. We detected the expression of choline acetyltransferase (ChAT), acetylcholinesterase (AChE), and the presence of ACh in MSCs. MSCs also expressed the nicotinic acetylcholine receptor subunits alpha 3, alpha 5, alpha 7, and the muscarinic acetylcholine receptor 2 (M2-receptor). The M2-receptor and the nicotinic alpha 7 receptor subunits were expressed on distinct subpopulations of cells, indicating differential regulation of cholinergic signaling between MSCs. Stimulation of MSCs with the nicotinic receptor agonist nicotine and the muscarinic receptor agonist muscarine induced immediate and transient increases in intracellular Ca(2+) concentration. Furthermore, muscarine had an inhibiting effect on the production of the intracellular signaling molecule cyclic adenosine 3',5'-monophosphate (cAMP). The AChE inhibitor chlorpyrifos, which is widely used as an agricultural insecticide, had similar effects on intracellular Ca(2+) and cAMP in MSCs. Nicotine, muscarine, and chlorpyrifos induced the phosphorylation of extracellular signal-regulated kinases 1 and 2. This study demonstrates that several components of a cholinergic signaling system are present and functional in MSCs. Environmental compounds such as nicotine and agricultural insecticides can interfere with this system and may affect cellular processes in the MSC.

PubMedSearch : Hoogduijn_2009_Stem.Cells.Dev_18_103
PubMedID: 18393628

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Citations formats

Hoogduijn MJ, Cheng A, Genever PG (2009)
Functional nicotinic and muscarinic receptors on mesenchymal stem cells
Stem Cells Dev 18 :103

Hoogduijn MJ, Cheng A, Genever PG (2009)
Stem Cells Dev 18 :103