Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Hypertonicity-induced cation channels.

F Wehner1, M Bondarava, F ter Veld

  • 1Max-Planck-Institut für molekulare Physiologie, Dortmund, Germany.

Acta Physiologica (Oxford, England)
|June 1, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Optimized Ki-67 staining in murine cells: a tool to determine cell proliferation.

Molecular biology reports·2019
Same author

[Use of nanoparticles in ophthalomology].

Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft·2011
Same author

Effects of somatostatin and octreotide on cytokine and chemokine production by lipopolysaccharide-activated peripheral blood mononuclear cells.

Journal of endocrinological investigation·2009
Same author

Basic molecular fingerprinting of immature cerebellar cortical inhibitory interneurons and their precursors.

Neuroscience·2009
Same author

Insulin-like growth factor-1 receptor acts as a growth regulator in synovial sarcoma.

The Journal of pathology·2008
Same author

Somatostatin receptor expression in peripheral blood of type 2 diabetes mellitus patients.

Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme·2007
Same journal

RyR1 Calcium Leak and Mitochondrial Ca<sup>2+</sup> Homeostasis in Skeletal Muscle.

Acta physiologica (Oxford, England)·2026
Same journal

Functional Differences in Electrolyte Transport Between the Mouse Proximal and Distal Trachea.

Acta physiologica (Oxford, England)·2026
Same journal

Of Mice and Men: Toward Mouse-Specific Diastolic Echocardiography.

Acta physiologica (Oxford, England)·2026
Same journal

Myosin Post-Translational Modifications Associated With Critical Illness Myopathy.

Acta physiologica (Oxford, England)·2026
Same journal

Phenylalanine Versus Tyrosine (Pos. 367/332 in MCT1/MCT4) in the Substrate Binding Site Defines Affinity and Preferred Directionality of Human Monocarboxylate Transporters 1-4.

Acta physiologica (Oxford, England)·2026
Same journal

Aberrant Potassium Handling by Astrocytes and Epileptic Seizures: A Synthetic Update.

Acta physiologica (Oxford, England)·2026
See all related articles

Hypertonicity-induced cation channels (HICCs) mediate cell volume regulation. These channels show varied responses to amiloride, Gd3+, and flufenamate, suggesting distinct subtypes involved in cell proliferation and apoptosis.

Area of Science:

  • Cell biology
  • Ion channel physiology

Background:

  • Hypertonicity-induced cation channels (HICCs) are key players in regulatory volume increase.
  • HICCs exhibit diverse pharmacological profiles, typically categorized by their sensitivity to amiloride or Gd3+/flufenamate.

Purpose of the Study:

  • To characterize the pharmacological and ion selectivity properties of HICCs.
  • To explore the molecular correlates and functional roles of HICCs in cellular processes.

Main Methods:

  • Quantitative electrophysiological studies to assess channel activity.
  • Pharmacological profiling using amiloride, Gd3+, and flufenamate.
  • Ion permeability assays to determine selectivity for various cations.

Main Results:

Related Experiment Videos

  • Two main HICC types were identified: amiloride-sensitive and amiloride-insensitive (Gd3+/flufenamate-sensitive).
  • Amiloride-insensitive HICCs display varied permeability to Na+, K+, Cs+, Li+, and NMDG+.
  • Potential molecular links to epithelial Na+ channels and transient receptor potential channels were suggested.
  • Conclusions:

    • HICCs are crucial for regulatory volume increase with distinct pharmacological subtypes.
    • These channels may influence cell proliferation, contrasting with K+ channels involved in apoptosis.
    • Further research is needed to elucidate the precise molecular identity and roles of HICCs.