“…After washing in PB, cells were permeabilized with 0.5% Triton X‐100 in PB for 10 min and submitted to epifluorescence protocol as described previously (Castro‐Raucci et al . ) using Alexa Fluor 488‐conjugated phalloidin (green fluorescence, 1:200, Molecular Probes, Invitrogen, Eugene, OR, USA) for actin cytoskeleton labelling and 300 nM 4′,6‐diamidino‐2‐phenylindole, dihydrochloride (blue fluorescence, DAPI, Molecular Probes) for cell nuclei staining. The samples were examined under epifluorescence using an AxioImager M2 Zeiss light microscope (Carl Zeiss Inc., Oberkochen, Germany) outfitted with an AxioCam MRM digital camera (Carl Zeiss Inc.).…”