Evidence map›Paper›PMID 8786429›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1996

Whole-cell chloride currents in rat astrocytes accompany changes in cell morphology.

C D Lascola, R P Kraig

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. Article
  3. Physiology of Astroglia.Physiological reviews · 2018
    Review
  4. Article
  5. Article
  6. Astrocytic plasticity and patterned oxytocin neuronal activity: dynamic interactions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Article
  7. Article
  8. Article
  9. Article
  10. Expression of voltage-gated chloride channels in human glioma cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2003
    Article
  11. Volume-activated chloride currents contribute to the resting conductance and invasive migration of human glioma cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
    Article
  12. Article
  13. Article
  14. Glutamate release through volume-activated channels during spreading depression.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  15. Modulation of glioma cell migration and invasion using Cl(-) and K(+) ion channel blockers.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  16. Involvement of stretch-activated Cl- channels in ramification of murine microglia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1998
    Article
  17. Article
  18. Cytoskeletal actin gates a Cl- channel in neocortical astrocytes.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1998
    Article
  19. Mitogen-activated protein and tyrosine kinases in the activation of astrocyte volume-activated chloride current.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1998
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

C D LascolaCommittee on Neurobiology, University of Chicago, Illinois 60637, USA.
R P Kraig
University of Chicago · US

Funding

HYDROGEN IONS AND BRAIN INFARCTIONR01NS019108 · NINDS · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI KRAIG, RICHARD P · 1985 to 2019
$5.2M
MAMMALIAN ASTROGLIAL NA-BICARBONATE COTRANSPORTF31MH011126 · NIMH · UNIVERSITY OF CHICAGO · PI LASCOLA, CHRISTOPHER D · 1995 to 1995
–
NICHD NIH HHS HD-07009NIMH NIH HHS F31-MH11126NINDS NIH HHS NS-19108NINDS NIH HHS R01 NS019108
6 · The paper itself

Abstract

Astrocytes can change shape dramatically in response to increased physiological and pathological demands, yet the functional consequences of morphological change are unknown. We report the expression of Cl- currents after manipulations that alter astrocyte morphology. Whole-cell Cl- currents were elicited after (1) rounding up cells by brief exposure to trypsin; (2) converting cells from a flat polygonal to a process-bearing (stellate) morphology by exposure to serum-free Ringer's solution; and (3) swelling cells by exposure to hypo-osmotic solution. Zero-current potentials approximated the Nernst for Cl-, and rectification usually followed that predicted by the constant-field equation. We observed heterogeneity in the activation and inactivation kinetics, as well as in the relative degree of outward versus inward rectification. Cl- conductances were inhibited by 4, 4-diisothiocyanostilbene-2,2'-disulfonic acid (200 microM) and by Zn2+ (1 mM). Whole-cell Cl- currents were not expressed in cells without structural change. We investigated whether changes in cytoskeletal actin accompanying changes in astrocytic morphology play a role in the induction of shape-dependent Cl- currents. Cytochalasins, which disrupt actin polymers by enhancing actin-ATP hydrolysis, elicited whole-cell Cl- conductances in flat, polygonal astrocytes. In stellate cells, elevated intracellular Ca2+ (2 microM), which can depolymerize actin, enhanced Cl- currents, and high intracellular ATP (5 mM), required for repolymerization, reduced Cl- currents. Modulation of Cl- current by Ca2+ and ATP was blocked by concurrent whole-cell dialysis with phalloidin and DNase, respectively. Phalloidin stabilizes actin polymers and DNase inhibits actin polymerization. Dialysis with phalloidin also prevented hypo-osmotically activated Cl- currents. These results demonstrate how the expression of astrocyte Cl- currents can be dependent on cell morphology, the structure of actin, Ca2+ homeostasis, and metabolism.

Indexed as

4,4'-Diisothiocyanostilbene-2,2'-Disulfonic AcidAction PotentialsAdenosine TriphosphateAnimalsAstrocytesCalciumCells, CulturedChloride ChannelsImmunohistochemistryPatch-Clamp TechniquesRatsZinc4,4'-Diisothiocyanostilbene-2,2'-Disulfonic AcidAdenosine TriphosphateCalciumChloride ChannelsZinc

Identifiers

PMID8786429
PMCPMC2695502
OpenAlexW1961610463

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.