|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Department of Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, United States
2 Department of Anesthesiology, University of Texas MD Anderson Cancer Center, Houston, Texas, United States
* To whom correspondence should be addressed. E-mail: ealtmd{at}aol.com.
Human adipose tissue-derived stem cells (hASCs) represent a potentially valuable cell source for clinical therapeutic applications. The present study was designed to investigate properties of ionic channel currents present in undifferentiated hASCs and their impact on hASC proliferation. The functional ion channels in hASCs were analyzed by whole-cell patch-clamp recording and their mRNA expression levels detected by RT-PCR. Four types of ion channels were found to be present in hASCs: most of the hASCs (73%) showed a delayed rectifier-like K+ current (IKDR); Ca2+-activated K+ current (IKCa) was detected in examined cells; a transient outward K+ current (Ito) was recorded in 19% of the cells; a small percentage of cells (8%) displayed a tetrodotoxin (TTX)-sensitive transient inward sodium current (INa.TTX). RT-PCR results confirmed the presence of ion channels at the mRNA level: Kv1.1, Kv2.1, Kv1.5, Kv7.3, Kv11.1 and hEAG1 possibly encoding IKDR; MaxiK, KCNN3 and KCNN4 for IKCa; Kv1.4, Kv4.1, Kv4.2 and Kv4.3 for Ito and hNE-Na for INa.TTX. The IKDR was inhibited by tetraethyl ammonium (TEA) and 4-aminopyridine (4-AP), which significantly reduced the proliferation of hASCs in a dose-dependent manner (p<0.05) as suggested by bromodeoxyurindine (BrdU) incorporation. Other selective potassium channel blockers including linopiridine, iberiotoxin, clotrimazole, and apamin also significantly inhibited IKDR. TTX completely abolished INa.TTX. This study demonstrates for the first time that multiple functional ion channel currents are present in undifferentiated hASCs and their potential physiological function in these cells, as a basic understanding for future in vitro experiments and in vivo clinical investigations.
This article has been cited by other articles:
![]() |
R. Tao, C.-P. Lau, H.-F. Tse, and G.-R. Li Regulation of cell proliferation by intermediate-conductance Ca2+-activated potassium and volume-sensitive chloride channels in mouse mesenchymal stem cells Am J Physiol Cell Physiol, November 1, 2008; 295(5): C1409 - C1416. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Morokuma, D. Blackiston, D. S. Adams, G. Seebohm, B. Trimmer, and M. Levin Modulation of potassium channel function confers a hyperproliferative invasive phenotype on embryonic stem cells PNAS, October 28, 2008; 105(43): 16608 - 16613. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. B. Claiborne, K. P. Choe, A. I. Morrison-Shetlar, J. C. Weakley, J. Havird, A. Freiji, D. H. Evans, and S. L. Edwards Molecular detection and immunological localization of gill Na+/H+ exchanger in the dogfish (Squalus acanthias) Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2008; 294(3): R1092 - R1102. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Visit Other APS Journals Online |