Calcium‐dependent potassium channels control proliferation of cardiac progenitor cells and bone marrow‐derived mesenchymal stem cells

다국어 초록 (Multilingual Abstract)

Ex vivo proliferated c‐Kit+ endogenous cardiac progenitor cells (eCPCs) obtained from mouse and human cardiac tissues have been reported to express a wide range of functional ion channels.
In contrast to previous reports in cultured c‐Kit+ eCPCs, we found that ion currents were minimal in freshly isolated cells. However, inclusion of free Ca2+ intracellularly revealed a prominent inwardly rectifying current identified as the intermediate conductance Ca2+‐activated K+ current (KCa3.1)
Electrical function of both c‐Kit+ eCPCs and bone marrow‐derived mesenchymal stem cells is critically governed by KCa3.1 calcium‐dependent potassium channels.
Ca2+‐induced increases in KCa3.1 conductance are necessary to optimize membrane potential during Ca2+ entry. Membrane hyperpolarization due to KCa3.1 activation maintains the driving force for Ca2+ entry that activates stem cell proliferation.
Cardiac disease downregulates KCa3.1 channels in resident cardiac progenitor cells. Alterations in KCa3.1 may have pathophysiological and therapeutic significance in regenerative medicine.

Endogenous c‐Kit+ cardiac progenitor cells (eCPCs) and bone marrow (BM)‐derived mesenchymal stem cells (MSCs) are being developed for cardiac regenerative therapy, but a better understanding of their physiology is needed. Here, we addressed the unknown functional role of ion channels in freshly isolated eCPCs and expanded BM‐MSCs using patch‐clamp, microfluorometry and confocal microscopy. Isolated c‐Kit+ eCPCs were purified from dog hearts by immunomagnetic selection. Ion currents were barely detectable in freshly isolated c‐Kit+ eCPCs with buffering of intracellular calcium (Ca2+i). Under conditions allowing free intracellular Ca2+, freshly isolated c‐Kit+ eCPCs and ex vivo proliferated BM‐MSCs showed prominent voltage‐independent conductances that were sensitive to intermediate‐conductance K+‐channel (KCa3.1 current, IKCa3.1) blockers and corresponding gene (KCNN4)‐expression knockdown. Depletion of Ca2+i induced membrane‐potential (Vmem) depolarization, while store‐operated Ca2+ entry (SOCE) hyperpolarized Vmem in both cell types. The hyperpolarizing SOCE effect was substantially reduced by IKCa3.1 or SOCE blockade (TRAM‐34, 2‐APB), and IKCa3.1 blockade (TRAM‐34) or KCNN4‐knockdown decreased the Ca2+ entry resulting from SOCE. IKCa3.1 suppression reduced c‐Kit+ eCPC and BM‐MSC proliferation, while significantly altering the profile of cyclin expression. IKCa3.1 was reduced in c‐Kit+ eCPCs isolated from dogs with congestive heart failure (CHF), along with corresponding KCNN4 mRNA. Under perforated‐patch conditions to maintain physiological [Ca2+]i, c‐Kit+ eCPCs from CHF dogs had less negative resting membrane potentials (−58 ± 7 mV) versus c‐Kit+ eCPCs from control dogs (−73 ± 3 mV, P < 0.05), along with slower proliferation. Our study suggests that Ca2+‐induced increases in IKCa3.1 are necessary to optimize membrane potential during the Ca2+ entry that activates progenitor cell proliferation, and that alterations in KCa3.1 may have pathophysiological and therapeutic significance in regenerative medicine.

Ex vivo proliferated c‐Kit+ endogenous cardiac progenitor cells (eCPCs) obtained from mouse and human cardiac tissues have been reported to express a wide range of functional ion channels.
In contrast to previous reports in cultured c‐Kit+ eCPCs, we found that ion currents were minimal in freshly isolated cells. However, inclusion of free Ca2+ intracellularly revealed a prominent inwardly rectifying current identified as the intermediate conductance Ca2+‐activated K+ current (KCa3.1)
Electrical function of both c‐Kit+ eCPCs and bone marrow‐derived mesenchymal stem cells is critically governed by KCa3.1 calcium‐dependent potassium channels.
Ca2+‐induced increases in KCa3.1 conductance are necessary to optimize membrane potential during Ca2+ entry. Membrane hyperpolarization due to KCa3.1 activation maintains the driving force for Ca2+ entry that activates stem cell proliferation.
Cardiac disease downregulates KCa3.1 channels in resident cardiac progenitor cells. Alterations in KCa3.1 may have pathophysiological and therapeutic significance in regenerative medicine.