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. 2011 May;178(5):2191–2204. doi: 10.1016/j.ajpath.2011.01.046

Table 2.

Phosphorylated Activation of Intracellular Signaling Molecules in Lung Alveolar Type II Epithelial Cells from CCSP-rtTA/(tetO)7-CMV-dnPPARγ Bitransgenic Mice

Percentage ratio (%)
MFI ratio (%)
−DOX +DOX −DOX +DOX
pStat1 10.37 ± 3.18 47.32 ± 5.92⁎⁎ 22.42 ± 9.18 66.65 ± 16.11⁎⁎
pStat2 9.54 ± 4.23 33.47 ± 6.12⁎⁎ 12.62 ± 2.79 27.78 ± 5.45⁎⁎
pStat3 6.47 ± 2.1 39.01 ± 8.31⁎⁎ 11.22 ± 3.13 41.22 ± 7.22⁎⁎
pStat4 11.18 ± 2.88 42.11 ± 4.35⁎⁎ 11.90 ± 2.74 14.72 ± 3.85
pStat5 23.79 ± 7.15 9.50 ± 4.69 30.09 ± 10.65 13.48 ± 3.01
pStat6 25.81 ± 6.8 10.07 ± 4.77 20.20 ± 5.22 18.48 ± 4.52
pErk 10.87 ± 1.55 33.78 ± 3.33⁎⁎ 18.86 ± 3.96 51.30 ± 7.76⁎⁎
pP38 14.51 ± 3.56 41.11 ± 10.49⁎⁎ 24.79 ± 5.56 59.05 ± 9.55⁎⁎

−DOX, doxycycline-untreated bitransgenic mice; +DOX, doxycycline-treated bitransgenic mice.

Cells isolated from the lung were stained with anti-SP-C antibody, followed by intranuclear staining with anti-phospho-Stat1-6, anti-phospho-Erk, or anti-phospho-P38 antibody, and Stat1-6, Erk, or P38 antibody as described under Materials and Methods. Numbers of percentage ratio and mean fluorescent intensity (MFI) ratio between phospho-proteins and total proteins in gated SP-C positive cells from four independent experiments (n = 4) were calculated and statistically analyzed.

P < 0.05;

⁎⁎

P < 0.01.