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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: J Cell Mol Med. 2011 Nov;15(11):2364–2376. doi: 10.1111/j.1582-4934.2010.01226.x

Table 1. Quantification of morphological changes caused by myc-SH3A expression in cultured ECs.

Fifty electron micrographs (30,000 × magnification) per experimental condition, containing ECs profiles of control and myc-SH3A transfected ECs were used to count the number of i) abnormal caveolae clusters open to the apical side of the endothelial PM, ii) apparently normal caveolae, omega-shaped, connected to the PM either directly or through short necks, iii) caveolae with their neck surrounded by staining dense collars and iv) caveolae with elongated necks (less than ½ of caveolar diameter). Quantification of these morphological characteristics and the measurement of the length PM on the electron micrograph used were performed as described previously [10, 28]. The data were normalized per 100 μm length PM and are averages ± SD of three independent experiments.

experimental condition abnormal caveolae clusters open to the apical side of EC apparently normal - omega shaped caveolae single caveolae with staining dense rings around the neck caveolae with elongated necks
control ECs 3 ± 0.4 82 ± 8 2 ± 0.3 8 ± 0.9
myc-SH3A transfected ECs 30 ± 5.3 15 ± 6.1 38 ± 4.2 34± 2.5