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. 2020 Jun 30;15:2633105520931966. doi: 10.1177/2633105520931966

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© The Author(s) 2020

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 4. — (A) N2A cells cultured in medium (M) and with PA63. Intensity of staining of MAP2 and p-cofilin combined. Cell nuclei are stained with DAPI (blue). (B) Intensity of staining for MAP2 and p-cofilin was ranked arbitrarily from 0 to 25. Intensity of staining for combined microtubular and actin networks was approximately 30% less in the presence of PA63 (B) (*P < .05). DAPI indicates 4′,6-diamidino-2-phenylindole; MAP2, microtubule-associated protein-2; N2A cells, neuroblastoma 2A cells; PA63, anthrax protective antigen 63.