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Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity.

Publication ,  Journal Article
Tong, J; Briggs, MM; McIntosh, TJ
Published in: Biophys J
November 7, 2012

Aquaporin-4 (AQP4) is the primary water channel in the mammalian brain, particularly abundant in astrocytes, whose plasma membranes normally contain high concentrations of cholesterol. Here we test the hypothesis that the water permeabilities of two naturally occurring isoforms (AQP4-M1 and AQP4-M23) depend on bilayer mechanical/structural properties modulated by cholesterol and phospholipid composition. Osmotic stress measurements were performed with proteoliposomes containing AQP4 and three different lipid mixtures: 1), phosphatidylcholine (PC) and phosphatidylglycerol (PG); 2), PC, PG, with 40 mol % cholesterol; and 3), sphingomyelin (SM), PG, with 40 mol % cholesterol. The unit permeabilities of AQP4-M1 were 3.3 ± 0.4 × 10(-13) cm(3)/s (mean ± SE), 1.2 ± 0.1 × 10(-13) cm(3)/s, and 0.4 ± 0.1 × 10(-13) cm(3)/s in PC:PG, PC:PG:cholesterol, and SM:PG:cholesterol, respectively. The unit permeabilities of AQP4-M23 were 2.1 ± 0.2 × 10(-13) cm(3)/s, 0.8 ± 0.1 × 10(-13) cm(3)/s, and 0.3 ± 0.1 × 10(-13) cm(3)/s in PC:PG, PC:PG:cholesterol, and SM:PG:cholesterol, respectively. Thus, for each isoform the unit permeabilities strongly depended on bilayer composition and systematically decreased with increasing bilayer compressibility modulus and bilayer thickness. These observations suggest that altering lipid environment provides a means of regulating water channel permeability. Such permeability changes could have physiological consequences, because AQP4 water permeability would be reduced by its sequestration into SM:cholesterol-enriched raft microdomains. Conversely, under ischemic conditions astrocyte membrane cholesterol content decreases, which could increase AQP4 permeability.

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Published In

Biophys J

DOI

EISSN

1542-0086

Publication Date

November 7, 2012

Volume

103

Issue

9

Start / End Page

1899 / 1908

Location

United States

Related Subject Headings

  • Water
  • Sphingomyelins
  • Saccharomyces cerevisiae
  • Rats
  • Protein Isoforms
  • Phosphatidylglycerols
  • Permeability
  • Osmosis
  • Liposomes
  • Elasticity
 

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Tong, J., Briggs, M. M., & McIntosh, T. J. (2012). Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity. Biophys J, 103(9), 1899–1908. https://doi.org/10.1016/j.bpj.2012.09.025
Tong, Jihong, Margaret M. Briggs, and Thomas J. McIntosh. “Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity.Biophys J 103, no. 9 (November 7, 2012): 1899–1908. https://doi.org/10.1016/j.bpj.2012.09.025.
Tong J, Briggs MM, McIntosh TJ. Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity. Biophys J. 2012 Nov 7;103(9):1899–908.
Tong, Jihong, et al. “Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity.Biophys J, vol. 103, no. 9, Nov. 2012, pp. 1899–908. Pubmed, doi:10.1016/j.bpj.2012.09.025.
Tong J, Briggs MM, McIntosh TJ. Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity. Biophys J. 2012 Nov 7;103(9):1899–1908.
Journal cover image

Published In

Biophys J

DOI

EISSN

1542-0086

Publication Date

November 7, 2012

Volume

103

Issue

9

Start / End Page

1899 / 1908

Location

United States

Related Subject Headings

  • Water
  • Sphingomyelins
  • Saccharomyces cerevisiae
  • Rats
  • Protein Isoforms
  • Phosphatidylglycerols
  • Permeability
  • Osmosis
  • Liposomes
  • Elasticity