Skip to main content
. 2012 Oct 29;199(3):513–525. doi: 10.1083/jcb.201206143

Figure 2.

Figure 2.

Cortical microtubules increase epidermal sheet integrity. (A) Epidermal sheet fragments resulting from mechanical disruption of untreated or taxol-treated keratinocytes. Bar, 1 cm. (B) Quantitation of sheet fragments resulting from mechanical disruption of keratinocyte monolayers. P = 0.0017 for control vs. taxol treatment; n = 5 for control, 7 for taxol treatment. (C) Quantitation of epidermal sheet stability in cells treated with normal rat serum (NRS) in the presence or absence of taxol and treated with the E-cadherin inhibitory antibodies, DECMA, in the presence or absence of taxol. P = 0.02. (D) Quantitation of epidermal sheet stability of α-catenin–null cells with and without taxol treatment. (E) Quantitation of epidermal sheet stability after treatment with the myosin II inhibitor (blebbistatin) with or without taxol (compare to control in B). (F) Epidermal sheet integrity in myosin IIA floxed cells, with or without Cre recombinase and taxol, as indicated. P < 0.0001. Error bars are SEM.