Korean J Physiol Pharmacol.  2008 Aug;12(4):131-135. 10.4196/kjpp.2008.12.4.131.

Characterization of Ionic Currents in Human Neural Stem Cells

Affiliations
  • 1Department of Physiology, College of Medicine, Dankook University, Cheonan, Korea. ansil67@dku.edu
  • 2Department of Physical Therapy, Gachon University of Medicine and Science Zucheon, Incheon, Korea.
  • 3Department of Anatomy, Ajou University School of Medicine, Suwon, Korea.

Abstract

The profile of membrane currents was investigated in differentiated neuronal cells derived from human neural stem cells (hNSCs) that were obtained from aborted fetal cortex. Whole-cell voltage clamp recording revealed at least 4 different currents: a tetrodotoxin (TTX)-sensitive Na+ current, a hyperpolarization-activated inward current, and A-type and delayed rectifier-type K+ outward currents. Both types of K+ outward currents were blocked by either 5 mM tetraethylammonium (TEA) or 5 mM 4-aminopyridine (4-AP). The hyperpolarization-activated current resembled the classical K+ inward current in that it exhibited a voltage-dependent block in the presence of external Ba2+ (30micrometer) or Cs+ (3micrometer). However, the reversal potentials did not match well with the predicted K+ equilibrium potentials, suggesting that it was not a classical K+ inward rectifier current. The other Na+ inward current resembled the classical Na+ current observed in pharmacological studies. The expression of these channels may contribute to generation and repolarization of action potential and might be regarded as functional markers for hNSCs-derived neurons.

Keyword

Human neural stem cells; TTX-sensitive Na+ current; A-type; delayed rectifier; hyperpolarization-activated inward current

MeSH Terms

4-Aminopyridine
Action Potentials
Humans
Membranes
Neural Stem Cells
Neurons
Tetraethylammonium
Tetrodotoxin
4-Aminopyridine
Tetraethylammonium
Tetrodotoxin

Figure

  • Fig. 1. Immunocytochemistry of differentiated human neural stem cells. Cultured hNSCs were differentiated into neural lineage cells by removing the growth factors from the culture medium. 9 days after neural induction, the cells were immunostained with (D~F) anti-β-tubulin III antibody (Tuj-1), and (G~I) anti- GFAP antibody. Immunostained cells were counterstained with DAPI. Phase contrast images of differentiated hNSCs at 100X, 200X, and 400X magnification are shown in (A~C).

  • Fig. 2. Voltage-dependent Na+ current in hNSCs. Membrane depolarization from −90 to 40 mV evoked inward currents (A), which were not observed when external Na+ was replaced with an equimolar concentration of NMG (B). The I~V relationships of (A) and (B) are shown in (C). Inward currents elicited by the same protocol are blocked completely by 500 nM TTX (D, E). The I~V relationships of (D) and (E) are shown in (F). Hollow circles indicate the amplitudes of peak inward currents of given commanding potentials in the control, and filled circles indicate the current amplitudes remaining after NMG substitution (C) or TTX application (F).

  • Fig. 3. Voltage-dependent K+ currents in hNSCs. Depolarizing pulses from −90 to 40 mV elicited outward K+ currents (A, B, D, E). The symbols above the currents traces indicate the measuring points. Hollow symbols are used in the control current traces, and filled symbols are used in the current traces remaining after the drug applications. I~V relationships before and after the drug applications are shown in (C, F). Hollow circles and squares in (C, F) indicate A-type and delayed rectifier type current amplitudes of each commanding potentials before drug application, while the filled symbols in (C, F) indicate amplitudes of A-type and delayed rectifier type currents after drug application.

  • Fig. 4. Hyperpolarization-activated inward currents in hNSCs. (A~C) Hyperpolarizing pulses from 0 to −130 mV elicited inward currents, which exhibited increases in amplitude with increases in the external concentration of K+ ([K+]ext). The I~V relationships of hyperpolarization-activated inward currents on external K+ concentrations are shown in (D: hollow circle – control, filled circle −30 mM [K+]ext, filled triangle −60 mM [K+]ext). The cesium (Cs) or barium (Ba) reversibly blocked the hyperpolarization-activated inward currents (E, F: hollow circle – control, filled circle – Cs or Ba, filled triangle – wash out).


Reference

Akesson E., Piao JH., Samuelsson EB., Holmberg L., Kjaeldgaard A., Falci S., Sundstrom E., Seiger A. Long-term culture and neuronal survival after intraspinal transplantation of human spinal cord-derived neurospheres. Physiol Behav. 92:60–66. 2007.
Artiani L., Bettiol E., Stillitano F., Mugelli A., Cerbai E., Jaconi ME. Developmental changes in cardiomyocytes differentiated from human embryonic stem cells: a molecular and electrophysiological approach. Stem Cells. 25:1136–1144. 2007.
Balasubramaniyan V., de Haas AH., Bakels R., Koper A., Boddeke HW., Copray JC. Functionally deficient neuronal differentiation of mouse embryonic neural stem cells in vitro. Neurosci Res. 49:261–265. 2004.
Article
Butt AM., Kalsi A. Inwardly rectifying potassium channels (Kir) in central nervous system glia: a special role for Kir4.1 in glial functions. J Cell Mol Med. 10:33–44. 2006.
Article
Buzańska L., Jurga M., Domańska-Janik K. Neuronal differentiation of human umbilical cord blood neural stem-like cell line. Neurodegener Dis. 3:19–26. 2006.
Article
Carpenter MK., Inokuma MS., Denham J., Mujtaba T., Chiu CP., Rao MS. Enrichment of neurons and neural precursors from human embryonic stem cells. Exp Neurol. 172:383–397. 2001.
Article
Cho T., Bae JH., Choi HB., Kim SS., McLarnon JG., Suh-Kim H., Kim SU., Min CK. Human neural stem cells: electrophysiological properties of voltage-gated ion channels. Neuroreport. 13:1447–1452. 2002.
Article
D'Ascenzo M., Piacentini R., Casalbore P., Budoni M., Pallini R., Azzena GB., Grassi C. Role of L-type Ca2+ channels in neural stem/progenitor cell differentiation. Eur J Neurosci. 23:935–944. 2006.
Doupnik CA., Davidson N., Lester HA. The inward rectifier potassium channel family. Curr Opin Neurobiol. 5:268–277. 1995.
Article
Flax JD., Aurora S., Yang C., Simonin C., Willis AM., Billinghurst LL., Jendoubi M., Sidman RL., Wolfe JH., Kim SU., Snyder EY. Engraftable human neural stem cells respond to developmental cues, replace neurons, and express foreign genes. Nat Biotechnol. 16:1033–1039. 1998.
Flynn ER., McManus CA., Bradley KK., Koh SD., Hegarty TM., Horowitz B., Sanders KM. Inward rectifier potassium conductance regulates membrane potential of canine colonic smooth muscle. J Physiol. 518(Pt 1):247–256. 1999.
Article
Ilancheran S., Michalska A., Peh G., Wallace EM., Pera M., Manuelpillai U. Stem cells derived from human fetal membranes display multilineage differentiation potential. Biol Reprod. 77:577–588. 2007.
Article
Johnson MA., Weick JP., Pearce RA., Zhang SC. Functional neural development from human embryonic stem cells: accelerated synaptic activity via astrocyte coculture. J Neurosci. 27:3069–3077. 2007.
Article
Li GR., Sun H., Deng X., Lau CP. Characterization of ionic currents in human mesenchymal stem cells from bone marrow. Stem Cells. 23:371–382. 2005.
Article
Mareschi K., Novara M., Rustichelli D., Ferrero I., Guido D., Carbone E., Medico E., Madon E., Vercelli A., Fagioli F. Neural differentiation of human mesenchymal stem cells: Evidence for expression of neural markers and eag K+ channel types. Exp Hematol. 34:1563–1572. 2006.
Moe MC., Westerlund U., Varghese M., Berg-Johnsen J., Svensson M., Langmoen LA. Development of neuronal networks from single stem cells harvested from the adult human brain. Neurosurgery. 56:1182–1188. 2005a.
Article
Moe MC., Varghese M., Danilov AI., Westerlund U., Ramm-Pettersen J., Brundin L., Svensson M., Berg-Johnsen J., Langmoen IA. Multipotent progenitor cells from the adult human brain: neurophysiological differentiation to mature neurons. Brain. 128:2189–2199. 2005b.
Article
Murata Y., Fujiwara Y., Kubo Y. Identification of a site involved in the block by extracellular Mg(2+) and Ba(2+) as well as permeation of K(+) in the Kir2.1 K(+) channel. J Physiol. 544:665–677. 2002.
Nichols CG., Lopatin AN. Inward rectifier potassium channels. Ann Rev Physiol. 47:11–39. 1997.
Article
Park KS., Jung KH., Kim SH., Kim KS., Choi MR., Kim Y., Chai YG. Functional expression of ion channels in mesenchymal stem cells derived from umbilical cord vein. Stem Cells. 25:2044–2052. 2007.
Article
Piper DR., Mujtaba T., Rao MS., Lucero MT. Immunocytochemical and physiological characterization of a population of cultured human neural precursors. J Neurophysiol. 84:534–548. 2000.
Article
Sun W., Buzanska L., Domanska-Janik K., Salvi RJ., Stachowiak MK. Voltage-sensitive and ligand-gated channels in differentiating neural stem-like cells derived from the nonhematopoietic fraction of human umbilical cord blood. Stem Cells. 23:931–945. 2005.
Article
Thompson GA., Leyland ML., Ashmole I., Sutcliffe MJ., Stanfield PR. Residues beyond the selectivity filter of the K+ channel kir2.1 regulate permeation and block by external Rb+ and Cs+. J Physiol. 526:231–240. 2000.
Weiss S., Reynolds BA., Vescovi AL., Morshead C., Craig CG., Van der Kooy D. Is there a neural stem cell in the mammalian forebrain? Trends Neurosci. 19:387–393. 1996.
Article
Westerlund U., Moe MC., Varghese MM., Berg-Johnsen J., Ohlsson M., Langmoen IA., Svensson M. Stem cells from the adult human brain develop into functional neurons in culture. Exp Cell Res. 289:378–383. 2003.
Article
Zahanich I., Graf EM., Heubach JF., Hempel U., Boxberger S., Ravens U. Molecular and functional expression of voltage-operated calcium channels during osteogenic differentiation of human mesenchymal stem cells. J Bone Miner Res. 20:1637–1646. 2005.
Article
Full Text Links
  • KJPP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr