Figure 7
Expression levels of phosphorylated VEGFR2 and MSK1 positively correlate with lymphatic markers in human skin tissues with hypertension. (A, B) Representative immunostaining of p-MSK1 (A) and p-VEGFR2 (B) in normotensive and hypertensive patients with quantification of integrated density per area at right. Scale bar: 50 μm. (C–F) Relationship of skin phosphorylated MSK1 (C), p-VEGFR2 (D), and podoplanin (E) expression and Na+ content (F) with systolic blood pressure in normotensive and hypertensive patients. (G) Model of lymphatic endothelial A2AR-mediated VEGF-independent activation of VEGFR2 signaling in dermal lymphangiogenesis and sodium balance. Data in (A) and (B) are presented as mean ± standard error mean and were analyzed by unpaired two-tailed t test. Data in (C)–(F) were analyzed by simple linear regression, and the Pearson correlation was calculated as the square root of r2. P < 0.05 was considered as statistically significant. intDen, integrated density.

Expression levels of phosphorylated VEGFR2 and MSK1 positively correlate with lymphatic markers in human skin tissues with hypertension. (A, B) Representative immunostaining of p-MSK1 (A) and p-VEGFR2 (B) in normotensive and hypertensive patients with quantification of integrated density per area at right. Scale bar: 50 μm. (C–F) Relationship of skin phosphorylated MSK1 (C), p-VEGFR2 (D), and podoplanin (E) expression and Na+ content (F) with systolic blood pressure in normotensive and hypertensive patients. (G) Model of lymphatic endothelial A2AR-mediated VEGF-independent activation of VEGFR2 signaling in dermal lymphangiogenesis and sodium balance. Data in (A) and (B) are presented as mean ± standard error mean and were analyzed by unpaired two-tailed t test. Data in (C)–(F) were analyzed by simple linear regression, and the Pearson correlation was calculated as the square root of r2. P < 0.05 was considered as statistically significant. intDen, integrated density.

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