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. 2018 Jan 11;55(8):6558–6571. doi: 10.1007/s12035-017-0861-3

Fig. 6.

Fig. 6

Intracellular retention of Cx43 in endoplasmic reticulum of MHV-A59-infected primary meningeal fibroblast cultures (af). Meningeal fibroblasts were mock-infected (ac) or infected with MHV-A59 (df), and double-immunostained for calnexin (green: b, e) and Cx43 (red: a, d). In infected cultures (df), Cx43 puncta are mostly seen in the perinuclear region which colocalize with ER marker calnexin (f; arrows). In control cells (ac), most of the Cx43 staining is observed towards the periphery (c; arrowheads) with only a few Cx43 puncta seen to colocalize with calnexin (c; arrow). Cells were counterstained with DAPI (blue) to visualize nuclear localization in merged images