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Regulation of connexin43 gap junctional communication by phosphatidylinositol 4,5-bisphosphate

Regulation of connexin43 gap junctional communication by phosphatidylinositol 4,5-bisphosphate
Regulation of connexin43 gap junctional communication by phosphatidylinositol 4,5-bisphosphate
Cell-cell communication through connexin43 (Cx43)-based gap junction channels is rapidly inhibited upon activation of various G protein-coupled receptors; however, the mechanism is unknown. We show that Cx43-based cell-cell communication is inhibited by depletion of phosphatidylinositol 4,5-bisphosphate (PtdIns[4,5]P(2)) from the plasma membrane. Knockdown of phospholipase Cbeta3 (PLCbeta3) inhibits PtdIns(4,5)P(2) hydrolysis and keeps Cx43 channels open after receptor activation. Using a translocatable 5-phosphatase, we show that PtdIns(4,5)P(2) depletion is sufficient to close Cx43 channels. When PtdIns(4,5)P(2) is overproduced by PtdIns(4)P 5-kinase, Cx43 channel closure is impaired. We find that the Cx43 binding partner zona occludens 1 (ZO-1) interacts with PLCbeta3 via its third PDZ domain. ZO-1 is essential for PtdIns(4,5)P(2)-hydrolyzing receptors to inhibit cell-cell communication, but not for receptor-PLC coupling. Our results show that PtdIns(4,5)P(2) is a key regulator of Cx43 channel function, with no role for other second messengers, and suggest that ZO-1 assembles PLCbeta3 and Cx43 into a signaling complex to allow regulation of cell-cell communication by localized changes in PtdIns(4,5)P(2).
Animals *Cell Communication Connexin 43/*metabolism Gap Junctions/*metabolism Humans Hydrolysis Isoenzymes/antagonists & inhibitors/chemistry/metabolism Membrane Proteins/chemistry/metabolism Mice Models, Neurological Phosphatidylinositol 4,5-Diphosphate/*metabolism Phospholipase C beta Phosphoproteins/chemistry/metabolism Protein Structure, Tertiary Rats Signal Transduction Type C Phospholipases/antagonists & inhibitors/chemistry/metabolism Zonula Occludens-1 Protein
0021-9525
881-891
van Zeijl, L.
f07b5b90-143b-4b65-b995-3cb797e69dfe
Ponsioen, B.
4807035a-4c91-42d7-8ea8-481646429924
Giepmans, B. N.
e8f087c2-4f7e-493e-b948-e96808150d99
Ariaens, A.
61e6be3f-5a18-4cfa-94b0-0898ddaeb8f8
Postma, F. R.
3ca3dd96-d78d-4107-b00c-ccc0596af4e1
Varnai, P.
158b2a15-7786-457a-9281-812b578481c6
Balla, T.
24387d5e-4345-4608-8d24-89c82cfe9316
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Jalink, K.
81124fdb-185d-43c1-a659-cd22dd2d381c
Moolenaar, W. H.
e97390b7-ebbe-485c-84e6-95fcab99182b
van Zeijl, L.
f07b5b90-143b-4b65-b995-3cb797e69dfe
Ponsioen, B.
4807035a-4c91-42d7-8ea8-481646429924
Giepmans, B. N.
e8f087c2-4f7e-493e-b948-e96808150d99
Ariaens, A.
61e6be3f-5a18-4cfa-94b0-0898ddaeb8f8
Postma, F. R.
3ca3dd96-d78d-4107-b00c-ccc0596af4e1
Varnai, P.
158b2a15-7786-457a-9281-812b578481c6
Balla, T.
24387d5e-4345-4608-8d24-89c82cfe9316
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Jalink, K.
81124fdb-185d-43c1-a659-cd22dd2d381c
Moolenaar, W. H.
e97390b7-ebbe-485c-84e6-95fcab99182b

van Zeijl, L., Ponsioen, B., Giepmans, B. N., Ariaens, A., Postma, F. R., Varnai, P., Balla, T., Divecha, N., Jalink, K. and Moolenaar, W. H. (2007) Regulation of connexin43 gap junctional communication by phosphatidylinositol 4,5-bisphosphate. Journal of Cell Biology, 177 (5), 881-891. (doi:10.1083/jcb.200610144).

Record type: Article

Abstract

Cell-cell communication through connexin43 (Cx43)-based gap junction channels is rapidly inhibited upon activation of various G protein-coupled receptors; however, the mechanism is unknown. We show that Cx43-based cell-cell communication is inhibited by depletion of phosphatidylinositol 4,5-bisphosphate (PtdIns[4,5]P(2)) from the plasma membrane. Knockdown of phospholipase Cbeta3 (PLCbeta3) inhibits PtdIns(4,5)P(2) hydrolysis and keeps Cx43 channels open after receptor activation. Using a translocatable 5-phosphatase, we show that PtdIns(4,5)P(2) depletion is sufficient to close Cx43 channels. When PtdIns(4,5)P(2) is overproduced by PtdIns(4)P 5-kinase, Cx43 channel closure is impaired. We find that the Cx43 binding partner zona occludens 1 (ZO-1) interacts with PLCbeta3 via its third PDZ domain. ZO-1 is essential for PtdIns(4,5)P(2)-hydrolyzing receptors to inhibit cell-cell communication, but not for receptor-PLC coupling. Our results show that PtdIns(4,5)P(2) is a key regulator of Cx43 channel function, with no role for other second messengers, and suggest that ZO-1 assembles PLCbeta3 and Cx43 into a signaling complex to allow regulation of cell-cell communication by localized changes in PtdIns(4,5)P(2).

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More information

Accepted/In Press date: 2 May 2007
Published date: 2007
Keywords: Animals *Cell Communication Connexin 43/*metabolism Gap Junctions/*metabolism Humans Hydrolysis Isoenzymes/antagonists & inhibitors/chemistry/metabolism Membrane Proteins/chemistry/metabolism Mice Models, Neurological Phosphatidylinositol 4,5-Diphosphate/*metabolism Phospholipase C beta Phosphoproteins/chemistry/metabolism Protein Structure, Tertiary Rats Signal Transduction Type C Phospholipases/antagonists & inhibitors/chemistry/metabolism Zonula Occludens-1 Protein

Identifiers

Local EPrints ID: 479388
URI: http://eprints.soton.ac.uk/id/eprint/479388
ISSN: 0021-9525
PURE UUID: 18cb9ee6-6f3e-42e3-a488-e791e615819a

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Date deposited: 20 Jul 2023 17:40
Last modified: 17 Mar 2024 03:00

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Contributors

Author: L. van Zeijl
Author: B. Ponsioen
Author: B. N. Giepmans
Author: A. Ariaens
Author: F. R. Postma
Author: P. Varnai
Author: T. Balla
Author: N. Divecha
Author: K. Jalink
Author: W. H. Moolenaar

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