Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries

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Standard

Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries. / Hald, Bjørn Olav; Welsh, Donald G; von Holstein-Rathlou, Niels-Henrik; Jacobsen, Jens Christian Brings.

I: Biophysical Journal, Bind 107, Nr. 10, 18.11.2014, s. 2467-76.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hald, BO, Welsh, DG, von Holstein-Rathlou, N-H & Jacobsen, JCB 2014, 'Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries', Biophysical Journal, bind 107, nr. 10, s. 2467-76. https://doi.org/10.1016/j.bpj.2014.09.036

APA

Hald, B. O., Welsh, D. G., von Holstein-Rathlou, N-H., & Jacobsen, J. C. B. (2014). Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries. Biophysical Journal, 107(10), 2467-76. https://doi.org/10.1016/j.bpj.2014.09.036

Vancouver

Hald BO, Welsh DG, von Holstein-Rathlou N-H, Jacobsen JCB. Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries. Biophysical Journal. 2014 nov. 18;107(10):2467-76. https://doi.org/10.1016/j.bpj.2014.09.036

Author

Hald, Bjørn Olav ; Welsh, Donald G ; von Holstein-Rathlou, Niels-Henrik ; Jacobsen, Jens Christian Brings. / Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries. I: Biophysical Journal. 2014 ; Bind 107, Nr. 10. s. 2467-76.

Bibtex

@article{802aebdd4096401c87683afbcae8e9d1,
title = "Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries",
abstract = "Despite stochastic variation in the molecular composition and morphology of individual smooth muscle and endothelial cells, the membrane potential along intact microvessels is remarkably uniform. This is crucial for coordinated vasomotor responses. To investigate how this electrical homogeneity arises, a virtual arteriole was developed that introduces variation in the activities of ion-transport proteins between cells. By varying the level of heterogeneity and subpopulations of gap junctions (GJs), the resulting simulations shows that GJs suppress electrical variation but can only reduce cytosolic [Ca(2+)] variation. The process of electrical smoothing, however, introduces an energetic cost due to permanent currents, one which is proportional to the level of heterogeneity. This cost is particularly large when electrochemically different endothelial-cell and smooth-muscle-cell layers are coupled. Collectively, we show that homocellular GJs in a passively open state are crucial for electrical uniformity within the given cell layer, but homogenization may be limited by biophysical or energetic constraints. Owing to the ubiquitous presence of ion transport-proteins and cell-cell heterogeneity in biological tissues, these findings generalize across most biological fields.",
author = "Hald, {Bj{\o}rn Olav} and Welsh, {Donald G} and {von Holstein-Rathlou}, Niels-Henrik and Jacobsen, {Jens Christian Brings}",
year = "2014",
month = nov,
day = "18",
doi = "10.1016/j.bpj.2014.09.036",
language = "English",
volume = "107",
pages = "2467--76",
journal = "Biophysical Journal",
issn = "0006-3495",
publisher = "Cell Press",
number = "10",

}

RIS

TY - JOUR

T1 - Gap junctions suppress electrical but not [Ca(2+)] heterogeneity in resistance arteries

AU - Hald, Bjørn Olav

AU - Welsh, Donald G

AU - von Holstein-Rathlou, Niels-Henrik

AU - Jacobsen, Jens Christian Brings

PY - 2014/11/18

Y1 - 2014/11/18

N2 - Despite stochastic variation in the molecular composition and morphology of individual smooth muscle and endothelial cells, the membrane potential along intact microvessels is remarkably uniform. This is crucial for coordinated vasomotor responses. To investigate how this electrical homogeneity arises, a virtual arteriole was developed that introduces variation in the activities of ion-transport proteins between cells. By varying the level of heterogeneity and subpopulations of gap junctions (GJs), the resulting simulations shows that GJs suppress electrical variation but can only reduce cytosolic [Ca(2+)] variation. The process of electrical smoothing, however, introduces an energetic cost due to permanent currents, one which is proportional to the level of heterogeneity. This cost is particularly large when electrochemically different endothelial-cell and smooth-muscle-cell layers are coupled. Collectively, we show that homocellular GJs in a passively open state are crucial for electrical uniformity within the given cell layer, but homogenization may be limited by biophysical or energetic constraints. Owing to the ubiquitous presence of ion transport-proteins and cell-cell heterogeneity in biological tissues, these findings generalize across most biological fields.

AB - Despite stochastic variation in the molecular composition and morphology of individual smooth muscle and endothelial cells, the membrane potential along intact microvessels is remarkably uniform. This is crucial for coordinated vasomotor responses. To investigate how this electrical homogeneity arises, a virtual arteriole was developed that introduces variation in the activities of ion-transport proteins between cells. By varying the level of heterogeneity and subpopulations of gap junctions (GJs), the resulting simulations shows that GJs suppress electrical variation but can only reduce cytosolic [Ca(2+)] variation. The process of electrical smoothing, however, introduces an energetic cost due to permanent currents, one which is proportional to the level of heterogeneity. This cost is particularly large when electrochemically different endothelial-cell and smooth-muscle-cell layers are coupled. Collectively, we show that homocellular GJs in a passively open state are crucial for electrical uniformity within the given cell layer, but homogenization may be limited by biophysical or energetic constraints. Owing to the ubiquitous presence of ion transport-proteins and cell-cell heterogeneity in biological tissues, these findings generalize across most biological fields.

U2 - 10.1016/j.bpj.2014.09.036

DO - 10.1016/j.bpj.2014.09.036

M3 - Journal article

C2 - 25418315

VL - 107

SP - 2467

EP - 2476

JO - Biophysical Journal

JF - Biophysical Journal

SN - 0006-3495

IS - 10

ER -

ID: 135658983