Author Correction: Live imaging-based assay for visualising species-specific interactions in gamete adhesion molecules
Kohdai P. Nakajima, Clari Valansi, Daisuke Kurihara, Narie Sasaki, Benjamin Podbilewicz, Tetsuya Higashiyama
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsSperm and Testicular Function
Correction to: Scientific Reports 10.1038/s41598-022-13547-w, published online 10 June 2022
The original version of the Article contained an error in Figure 2. As a result of an error during figure assembly, the 6:30 image in Figure 2A was mistakenly a duplication of the 8:30 image.
The original Figure 2 and accompanying legend appear below.Fig. 2. Adhesion molecules accumulated at the contact interface of adjacent cells. (A) Time-lapse images of E-cadherin-expressing cells. Box indicates the region where cell membrane fluorescent intensity was measured in (B). Time (h:min) since the start of observation is shown (see Video 2). Bar: 20 µm. (B) Fluorescence intensity profile of cells shown at the top. (Left panel) Cells prior to contact; (middle) cells immediately after contact; (right) cells immediately after detachment. (C) Time-lapse images of IZUMO1-expressing cells (green) and JUNO expressing-cells (magenta). Time (h:min) since the start of observation is shown (see Video 3). Bar: 20 µm. Arrowheads indicate IZUMO1 accumulation at the contact site. (D) Fluorescence intensity profile of IZUMO1 in a cell shown at the top. (E) IZUMO1 accumulation rate for various treatment combinations. Numbers indicate contacted cell pairs observed by live imaging.
The original Article has been corrected.