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Research Article
Plasma membrane rafts of rainbow trout are subject to thermal acclimation
John K. Zehmer, Jeffrey R. Hazel
Journal of Experimental Biology 2003 206: 1657-1667; doi: 10.1242/jeb.00346
John K. Zehmer
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Jeffrey R. Hazel
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  • Fig. 1.
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    Fig. 1.

    Detergent analyses. (A) Diagrammatic representation of detergent–membrane interaction. Loosely packed raft-depleted plasma membrane (RDPM) accommodates more detergent prior to saturation (higher saturation point; plate 1) than tightly packed raft (plate 2). After saturation occurs, mixed micelles form, dissolving the membrane. Lipids in RDPM are more readily incorporated into micelles (steeper solubilization slope; plate 3) than are raft lipids (plate 4). (B) Detergent assay. Membrane dissolution is followed as changes in optical density (OD) over time. End points are recorded as optical density just prior to detergent addition (arrow). Inset: normalized end points as a function of detergent/lipid (D/L) ratios with sigmoidal regression. (C) Analysis. Sigmoidal regression with D/L values of 2nd-derivative peaks marked (points a and b) with the linear regression between points a and b superimposed. Inset: 2nd derivative with peaks marked (points a and b). Saturation point (i.e. where solubilization becomes dominant over detergent incorporation) is defined by point a. Solubilization slope is defined as the slope of the linear regression between points a and b.

  • Fig. 2.
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    Fig. 2.

    Western blots. (A) Distribution of caveolin in trout kidney (Kid), spleen (Spl), adipose (Adi) and liver (Liv). All lanes, 15 μg total protein. (B–E) Samples loaded: 30 μg crude homogenate (Hom) and 15 μg plasma membrane (PM), raft-depleted PM (RDPM) and raft-enriched PM (raft). Probed with (B) antibodies against β2 adrenergic receptor (β2AR), (C) adenylyl cyclase (AC), (D) insulin receptor β subunit (IRβ) and (E) clathrin (Clath).

  • Fig. 3.
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    Fig. 3.

    Compositional analyses of membrane fractions. (A) Compositional comparisons of membrane fractions from cold-acclimated (open bars) and warm-acclimated (filled bars) fish expressed as ratios. (A) Cholesterol/protein (Ch/Pr). (B) Phospholipid/protein (PL/Pr). (C) Cholesterol/phospholipid (Chl/PL). Values are means ± S.E.M., N=6. Bars with a common lower-case letter do not differ significantly. PM, plasma membrane; RDPM, raft-depleted plasma membrane.

  • Table 1.

    Percentage composition of membrane fractions from cold- and warm-acclimated animals

    % Composition
    AnimalMembrane fractionCholesterolPhospholipidProtein
    Warm-acclimatedPM9.5±0.423.1±1.167.4±0.8
    RDPM10.0±0.423.0±1.567.0±1.3
    Raft16.1±1.027.6±1.556.3±1.2
    Cold-acclimatedPM8.5±0.325.4±0.666.1±0.7
    RDPM7.3±0.227.5±1.065.2±1.1
    Raft11.5±1.335.9±3.352.7±2.2
    • Values are means ± S.E.M. (N=6) and are based on the assumption that cholesterol, phospholipid and protein content add up to 100% of the membrane.

      PM, plasma membrane; RDPM, raft-depleted plasma membrane.

  • Fig. 4.
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    Fig. 4.

    Effects of temperature and cholesterol content on saturation point. (A) Symmetric methylene vibrational rates of myristoylpalmitoyl phosphatidylcholine (MPPC) vesicles as a function of temperature (circles). Saturation points of MPPC vesicles as a function of temperature (bars). Values are means ± range, N=2. (B) Saturation points of palmitoyloleoyl phosphatidylcholine (POPC) and POPC + 30 mol% cholesterol vesicles at 25°C. Values are means ± range, N=2.

  • Fig. 5.
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    Fig. 5.

    Effects of temperature and cholesterol content on solubilization slope. Values are means ± range, N=2. Absolute values of slopes of near-linear regions between 2nd-derivative peaks of fitted sigmoidal curves for (A) myristoylpalmitoyl phosphatidylcholine (MPPC) vesicles as a function of temperature and (B) palmitoyloleoyl phosphatidylcholine (POPC) and POPC + 30 mol% cholesterol vesicles at 25°C.

  • Fig. 6.
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    Fig. 6.

    Detergent solubility curves. Decline in normalized optical density (OD) as a function of detergent/lipid (D/L) ratios. Values are means ± S.E.M., N=4. Cold-acclimated samples assayed at 5°C (other data not shown). PM, plasma membrane; RDPM, raft-depleted plasma membrane.

  • Fig. 7.
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    Fig. 7.

    Saturation points. Bars with a common lower-case letter do not differ significantly. (A) Effects of acclimation group and fraction (data collapsed across assay temperature). Cold-acclimated, open bars; warm-acclimated, filled bars. Values are means ± S.E.M., N=8. (B) Effects of assay temperature (data collapsed across fraction and acclimation group). Values are means ± S.E.M., N=24. PM, plasma membrane; RDPM, raft-depleted plasma membrane.

  • Fig. 8.
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    Fig. 8.

    Saturation points, all comparisons. Values are means ± S.E.M., N=4. Cold-acclimated, open bars; warm-acclimated, filled bars. Dots denote measurements made at physiological temperatures. PM, plasma membrane; RDPM, raft-depleted plasma membrane.

  • Fig. 9.
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    Fig. 9.

    Saturation points, elevated assay temperature. Values are means ± S.E.M., N=4. Asterisks denote significant difference from values at 20°C (P<0.05). RDPM, raft-depleted plasma membrane.

  • Fig. 10.
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    Fig. 10.

    Slopes. Absolute values of slopes of near-linear regions between 2nd-derivative peaks of fitted sigmoidal curves (data collapsed across assay temperature). Cold-acclimated, open bars; warm-acclimated, filled bars. Values are means ± S.E.M., N=8. Bars with a common lower-case letter do not differ significantly. PM, plasma membrane; RDPM, raft-depleted plasma membrane.

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Research Article
Plasma membrane rafts of rainbow trout are subject to thermal acclimation
John K. Zehmer, Jeffrey R. Hazel
Journal of Experimental Biology 2003 206: 1657-1667; doi: 10.1242/jeb.00346
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Research Article
Plasma membrane rafts of rainbow trout are subject to thermal acclimation
John K. Zehmer, Jeffrey R. Hazel
Journal of Experimental Biology 2003 206: 1657-1667; doi: 10.1242/jeb.00346

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