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Mix and match: Investigating heteromeric and heterotypic gap junction channels in model systems and native tissues
- Publication Year :
- 2014
-
Abstract
- This review is based in part on a roundtable discussion session: “Physiological roles for heterotypic/heteromeric channels” at the 2013 International Gap Junction Conference (IGJC 2013) in Charleston, South Carolina. It is well recognized that multiple connexins can specifically co-assemble to form mixed gap junction channels with unique properties as a means to regulate intercellular communication. Compatibility determinants for both heteromeric and heterotypic gap junction channel formation have been identified and associated with specific connexin amino acid motifs. Hetero-oligomerization is also a regulated process; differences in connexin quality control and monomer stability are likely to play integral roles to control interactions between compatible connexins. Gap junctions in oligodendrocyte:astrocyte communication and in the cardiovascular system have emerged as key systems where heterotypic and heteromeric channels have unique physiologic roles. There are several methodologies to study heteromeric and heterotypic channels that are best applied to either heterologous expression systems, native tissues or both. There remains a need to use and develop different experimental approaches in order to understand the prevalence and roles for mixed gap junction channels in human physiology.
- Subjects :
- South carolina
Gap junction
Molecular Sequence Data
Biophysics
Connexin
Biology
Biochemistry
Article
Connexins
03 medical and health sciences
0302 clinical medicine
Structural Biology
Genetics
Animals
Humans
Amino Acid Sequence
Molecular Biology
030304 developmental biology
0303 health sciences
Membrane transport
Amino Acid Motifs
Quality control
Gap Junctions
Cell Biology
Human physiology
Protein multimerization
Cell biology
Protein Transport
Gap junction channel
Protein Multimerization
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....e4834b94aaa5843d4f870204bb0eb68d