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The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

TRPC6 is a candidate channel involved in receptor-stimulated cation currents in A7r5 smooth muscle cells

Jung, Silke, Strotmann, Rainer, Schultz, Günter, Plant, Tim D.·2002·American Journal of Physiology-Cell Physiology

Abstract

To investigate the possible role of members of the mammalian transient receptor potential (TRP) channel family (TRPC1–7) in vasoconstrictor-induced Ca 2+ entry in vascular smooth muscle cells, we studied [Arg 8]-vasopressin (AVP)-activated channels in A7r5 aortic smooth muscle cells. AVP induced an increase in free cytosolic Ca 2+ concentration ([Ca 2+]i) consisting of Ca 2+ release and Ca 2+ influx. Whole cell recordings revealed the activation of a nonselective cation current with a doubly rectifying current-voltage relation strikingly similar to those described for some heterologously expressed TRPC isoforms. The current was also stimulated by direct activation of G proteins as well as by activation of the phospholipase Cγ-coupled platelet-derived growth factor receptor. Currents were not activated by store depletion or increased [Ca 2+]i. Application of 1-oleoyl-2-acetyl- sn-glycerol stimulated the current independently of protein kinase C, a characteristic property of the TRPC3/6/7 subfamily. Like TRPC6-mediated currents, cation currents in A7r5 cells were increased by flufenamate. Northern hybridization revealed mRNA coding for TRPC1 and TRPC6. We therefore suggest that TRPC6 is a molecular component of receptor-stimulated Ca 2+-permeable cation channels in A7r5 smooth muscle cells.

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Metadata

Authors
Jung, S., Strotmann, R., Schultz, G., & Plant, T. D.
Venue
American Journal of Physiology-Cell Physiology
Published
2002-02-01
Volume
282
Issue
2
Pages
C347-C359
ISSN
  • 0363-6143 (ISSN-L)
  • 1522-1563
OpenAlex
W2053209167
Cited by
230
References
3
FWCI
8.88
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: TRPC6 is a candidate channel involved in receptor-stimulated cation currents in A7r5 smooth muscle cells. https://app.cochat.ai/papers/10.1152/ajpcell.00283.2001
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Jung, S., Strotmann, R., Schultz, G., & Plant, T. D. (2002). TRPC6 is a candidate channel involved in receptor-stimulated cation currents in A7r5 smooth muscle cells. American Journal of Physiology-Cell Physiology. https://doi.org/10.1152/ajpcell.00283.2001

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.