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Na+ current properties in islet alpha- and beta-cells reflect cell-specific Scn3a and Scn9a expression

Zhang, Q. (author)
Chibalina, M. V. (author)
Bengtsson, M. (author)
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Groschner, L. N. (author)
Ramracheya, R. (author)
Rorsman, N. J. G. (author)
Leiss, V. (author)
Nassar, M. A. (author)
Welling, A. (author)
Gribble, F. M. (author)
Reimann, F. (author)
Hofmann, F. (author)
Wood, J. N. (author)
Ashcroft, Frances M. (author)
Rorsman, Patrik, 1959 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology
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 (creator_code:org_t)
2014-10-31
2014
English.
In: Journal of Physiology-London. - : Wiley. - 0022-3751 .- 1469-7793. ; 592:21, s. 4677-4696
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • - and -cells express both Na(v)1.3 and Na(v)1.7 Na+ channels but in different relative amounts. The differential expression explains the different properties of Na+ currents in - and -cells. Na(v)1.3 is the functionally important Na+ channel subunit in both - and -cells. Islet Na(v)1.7 channels are locked in an inactive state due to an islet cell-specific factor. Mouse pancreatic - and -cells are equipped with voltage-gated Na+ currents that inactivate over widely different membrane potentials (half-maximal inactivation (V-0.5) at -100mV and -50mV in - and -cells, respectively). Single-cell PCR analyses show that both - and -cells have Na(v)1.3 (Scn3) and Na(v)1.7 (Scn9a) subunits, but their relative proportions differ: -cells principally express Na(v)1.7 and -cells Na(v)1.3. In -cells, genetically ablating Scn3a reduces the Na+ current by 80%. In -cells, knockout of Scn9a lowers the Na+ current by >85%, unveiling a small Scn3a-dependent component. Glucagon and insulin secretion are inhibited in Scn3a(-/-) islets but unaffected in Scn9a-deficient islets. Thus, Na(v)1.3 is the functionally important Na+ channel subunit in both - and -cells because Na(v)1.7 is largely inactive at physiological membrane potentials due to its unusually negative voltage dependence of inactivation. Interestingly, the Na(v)1.7 sequence in brain and islets is identical and yet the V-0.5 for inactivation is >30mV more negative in -cells. This may indicate the presence of an intracellular factor that modulates the voltage dependence of inactivation.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

GATED SODIUM-CHANNELS
K-ATP CHANNELS
MOUSE PANCREATIC-ISLETS
B-CELLS
GLUCAGON-SECRETION
INSULIN-SECRETION
DELTA-CELLS
GLUCOSE-HOMEOSTASIS
DIABETES-MELLITUS
INTACT ISLETS
Neurosciences
Physiology
SLER S
1992
DIABETES
V41
P1221
ESSEL DM
1990
JOURNAL OF MEMBRANE BIOLOGY
V116
P273

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art (subject category)

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