TRP Channels and calcium signalling in dental pulp stem cells


Autoria(s): El Karim, Ikhlas; Linden, Gerard; Curtis, Timothy; About, Imad; Irwin, Christopher; Lundy, Fionnuala
Data(s)

2014

Resumo

Introduction: Ca2+ ion is an important intracellular messenger essential for the regulation of various cellular functions including proliferation, differentiation and apoptosis. Transient Receptor Potential (TRP) channels are calcium permeable cationic channels that play important role in regulation of free intracellular calcium ([Ca2+]i) in response to thermal, physical and chemical stimuli. Ca2+ signalling in human dental pulp stem cells (hDPSCs) and the ion channels regulating Ca2+ are largely not known. Objectives: Investigate changes in [Ca2+]i and determine the ion channels that regulate calcium signalling in hDPSCs. Methods: DPSCs were derived from immature third molars and cells less than passage 6 were used in all the experiments. Changes in [Ca2+]i were studied with Fura2 calcium imaging. RNA was extracted from DPSCs and a panel of TRP channel gene expression was determined by qPCR employing custom designed FAM TRP specific primers and probes (Roche, UK) and the Light Cycler 480 Probes Master (Roche). Results: hDPSCs express gene transcripts for all TRP families including TRPV1, V2, V4, TRPA1, TRPC3, TRPC5, TRPC6, TRPM3, TRPM7 and TRPP2. Stimulation of cells with appropriate TRP channel agonist induced increase in [Ca2+]i and similar responses were obtained when cell were mechanically stimulated by membrane stretch with application of hypotonic solution. Conclusion: TRP channels mediate calcium signalling in hDPSCs that merit further investigation.

Identificador

http://pure.qub.ac.uk/portal/en/publications/trp-channels-and-calcium-signalling-in-dental-pulp-stem-cells(587918f8-d434-433c-98fc-0a92af3a0b93).html

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

El Karim , I , Linden , G , Curtis , T , About , I , Irwin , C & Lundy , F 2014 , ' TRP Channels and calcium signalling in dental pulp stem cells ' .

Tipo

conferenceObject