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. 2011 Nov 11;302(3):H770–H781. doi: 10.1152/ajpheart.00733.2011

Table 3.

Effects of constitutive overexpression of PLM S68E on levels of selected proteins

Wild-type ConS68E
4 wk
    NCX1 260.5 ± 9.2 (5) 244.1 ± 9.5 (4)
    SERCA2 151.1 ± 5.5 101.3 ± 6.2*
    α1, Na+-K+-ATPase 109.5 ± 11.9 101.4 ± 9.8
    α2, Na+-K+-ATPase 161.6 ± 5.9 161.4 ± 7.2
    Cav1.2 111.1 ± 12.6 135.3 ± 2.5*
    RyR2 184.0 ± 14.3 192.5 ± 48.8
    p-RyR2 160.2 ± 21.4 123.0 ± 17.3
    Calsequestrin 380.2 ± 13.2 330.3 ± 31.0
22 wk
    NCX1 223.4 ± 2.3 (5) 225.9 ± 6.9 (4)
    SERCA2 526.2 ± 27.0 529.6 ± 43.1
    α1, Na+-K+-ATPase 218.0 ± 9.4 196.2 ± 5.8
    α2, Na+-K+-ATPase 91.8 ± 17.3 105.4 ± 22.3
    Calsequestrin 465.9 ± 21.1 416.0 ± 39.6

Values (in arbitrary units) are means ± SE. Numbers in parentheses are numbers of hearts. NCX1, cardiac Na+/Ca2+ exchanger; PLM, phospholemman; SERCA2, sarco(endo)plasmic reticulum Ca2+-ATPase; Cav1.2, α-subunit of L-type Ca2+ channel; RyR2, cardiac ryanodine receptor; p-RyR2, ryanodine receptor phosphorylated at serine2808.

*

P < 0.02, wild-type versus conS68E.