The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability

Yosuke Nakazawa, Mikako Oka, Katsuya Furuki, Akiko Mitsuishi, Emi Nakashima, Makoto Takehana

Research output: Contribution to journalArticle

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Abstract

Purpose: To study the interaction between the lens-specific water channel protein, aquaporin 0 (AQP0) and the lensspecific intermediate filament protein, filensin, and the effect of this interaction on the water permeability of AQP0. The effect of other factors on the interaction was also investigated. Methods: Expression plasmids were constructed in which glutathione-S-transferase (GST) was fused to the AQP0 COOHterminal region (GST-AQP0-C), which contains the major phosphorylation sites of the protein. Plasmids for AQP0 COOHterminal mutants were also constructed in which one, three or five sites were pseudophosphorylated, and the proteins expressed from these GST-fusion plasmids were assayed for their interaction with lens proteins. Expressed recombinant GST-fusion proteins were purified using glutathione beads and incubated with rat lens extract. Western blotting was used to identify the lens proteins that interacted with the GST-fusion proteins. Filensin tail and rod domains were also expressed as GST-fusion proteins and their interactions with AQPO were analyzed. Additionally, the water permeability of AQP0 was calculated by expressing AQP0 with or without the filensin peptide on the cell membrane of Xenopus oocytes by injecting cRNAs for AQP0 and filensin. Results: The GST-AQP0-C construct interacted with the tail region of lens filensin and the GST-filensin-tail construct interacted with lens AQP0, but the GST-filensin-rod construct did not interact with AQP0. GST-AQP0-C also interacted with a purified recombinant filensin-tail peptide after cleavage from GST. The AQP0/filensin-tail interaction was not affected by pseudophosphorylation of the AQP0 COOH-terminal tail, nor was it affected by changes in pH. Xenopus oocytes expressing AQP0 on the plasma membrane showed increased water permeability, which was lowered when the filensin COOH-terminal peptide cRNA was coinjected with the cRNA for AQP0. Conclusions: The filensin COOH-terminal tail region interacted with the AQP0 COOH-terminal region and the results strongly suggested that the interaction was direct. It appears that interactions between AQP0 and filensin helps to regulate the water permeability of AQP0 and to organize the structure of lens fiber cells, and may also help to maintain the transparency of the lens.

Original languageEnglish
Pages (from-to)3191-3199
Number of pages9
JournalMolecular Vision
Volume17
Publication statusPublished - 2011 Dec 13

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Tail
Permeability
Glutathione Transferase
Water
Lenses
Complementary RNA
filensin
aquaporin 0
Crystallins
Plasmids
Xenopus
Proteins
Peptides
Oocytes
Cell Membrane
Intermediate Filament Proteins
Aquaporins
Glutathione

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Nakazawa, Y., Oka, M., Furuki, K., Mitsuishi, A., Nakashima, E., & Takehana, M. (2011). The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability. Molecular Vision, 17, 3191-3199.

The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability. / Nakazawa, Yosuke; Oka, Mikako; Furuki, Katsuya; Mitsuishi, Akiko; Nakashima, Emi; Takehana, Makoto.

In: Molecular Vision, Vol. 17, 13.12.2011, p. 3191-3199.

Research output: Contribution to journalArticle

Nakazawa, Y, Oka, M, Furuki, K, Mitsuishi, A, Nakashima, E & Takehana, M 2011, 'The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability', Molecular Vision, vol. 17, pp. 3191-3199.
Nakazawa, Yosuke ; Oka, Mikako ; Furuki, Katsuya ; Mitsuishi, Akiko ; Nakashima, Emi ; Takehana, Makoto. / The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability. In: Molecular Vision. 2011 ; Vol. 17. pp. 3191-3199.
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abstract = "Purpose: To study the interaction between the lens-specific water channel protein, aquaporin 0 (AQP0) and the lensspecific intermediate filament protein, filensin, and the effect of this interaction on the water permeability of AQP0. The effect of other factors on the interaction was also investigated. Methods: Expression plasmids were constructed in which glutathione-S-transferase (GST) was fused to the AQP0 COOHterminal region (GST-AQP0-C), which contains the major phosphorylation sites of the protein. Plasmids for AQP0 COOHterminal mutants were also constructed in which one, three or five sites were pseudophosphorylated, and the proteins expressed from these GST-fusion plasmids were assayed for their interaction with lens proteins. Expressed recombinant GST-fusion proteins were purified using glutathione beads and incubated with rat lens extract. Western blotting was used to identify the lens proteins that interacted with the GST-fusion proteins. Filensin tail and rod domains were also expressed as GST-fusion proteins and their interactions with AQPO were analyzed. Additionally, the water permeability of AQP0 was calculated by expressing AQP0 with or without the filensin peptide on the cell membrane of Xenopus oocytes by injecting cRNAs for AQP0 and filensin. Results: The GST-AQP0-C construct interacted with the tail region of lens filensin and the GST-filensin-tail construct interacted with lens AQP0, but the GST-filensin-rod construct did not interact with AQP0. GST-AQP0-C also interacted with a purified recombinant filensin-tail peptide after cleavage from GST. The AQP0/filensin-tail interaction was not affected by pseudophosphorylation of the AQP0 COOH-terminal tail, nor was it affected by changes in pH. Xenopus oocytes expressing AQP0 on the plasma membrane showed increased water permeability, which was lowered when the filensin COOH-terminal peptide cRNA was coinjected with the cRNA for AQP0. Conclusions: The filensin COOH-terminal tail region interacted with the AQP0 COOH-terminal region and the results strongly suggested that the interaction was direct. It appears that interactions between AQP0 and filensin helps to regulate the water permeability of AQP0 and to organize the structure of lens fiber cells, and may also help to maintain the transparency of the lens.",
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AU - Nakazawa, Yosuke

AU - Oka, Mikako

AU - Furuki, Katsuya

AU - Mitsuishi, Akiko

AU - Nakashima, Emi

AU - Takehana, Makoto

PY - 2011/12/13

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