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. 2019 Apr 4;4(7):e128935. doi: 10.1172/jci.insight.128935

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia

Valeria Tomati, Emanuela Caci, Loretta Ferrera, Emanuela Pesce, Elvira Sondo, Deborah M Cholon, Nancy L Quinney, Susan E Boyles, Andrea Armirotti, Roberto Ravazzolo, Luis JV Galietta, Martina Gentzsch, Nicoletta Pedemonte
PMCID: PMC6483642  PMID: 30944255

Original citation: JCI Insight. 2018;3(3):e98699. https://doi.org/10.1172/jci.insight.98699

Citation for this corrigendum: JCI Insight. 2019;4(7):e128935. https://doi.org/10.1172/jci.insight.128935

The unit for the concentration of peptide in the proliferation study was incorrectly reported in the Results and Methods sections and the Figure 4 legend. The corrected sentences, with sections indicated, are below.

Results

Evaluation of Tα-1 sequence and its effect on proliferation and apoptosis of MCF-7 breast cancer cells.

Therefore, we plated MCF-7 at low density on 96-well plates suitable for confocal high-content imaging and evaluated cell proliferation for 72 hours following treatment with Tα-1 (100 μM) or scrambled peptide (100 μM).

Methods

Proliferation study.

MCF-7 cells were plated at low density (10,000 cells/well) on 96-well plates suitable for high-content imaging. After 6 hours, cells were treated with the scrambled peptide (100 μM) or with Tα-1 (100 μM).

Figure 4 legend

(A) Dot plot showing proliferation of MCF-7 cells after 72-hour treatment with Tα-1 (100 μM) or scrambled peptide (100 μM, control). (B) Dot plot showing the number of apoptotic MCF-7 cells after 72-hour treatment with Tα-1 (100 μM) or scrambled peptide (100 μM, control).

The article has been updated to reflect these changes.

The authors regret the errors.

Version 1. 04/04/2019

Electronic publication

Footnotes


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