Literature DB >> 25885692

Correction: Transforming growth factor β and insulin signal changes in stromal fibroblasts of individual keratoconus patients.

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Abstract

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Year:  2015        PMID: 25885692      PMCID: PMC4401512          DOI: 10.1371/journal.pone.0126201

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


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There is an error in the legend for Fig 3. Please see the complete, corrected Fig 3 here.
Fig 3

ALK1 and ALK5 expression in DN and KC reverted-keratocytes.

Reverted donor (white bars) and patient (black bars) keratocytes maintained in DMEM:F12/ITS/phosphoascorbic acid for 4 days were switched to DMEM:F12 without ITS (BL), 2ng/ml TGFβ1 was added and cells harvested at 0–120 min for total RNA isolation. Fold change in gene expression relative to GAPDH was calculated as 2-ΔΔCt.

ALK1 and ALK5 expression in DN and KC reverted-keratocytes.

Reverted donor (white bars) and patient (black bars) keratocytes maintained in DMEM:F12/ITS/phosphoascorbic acid for 4 days were switched to DMEM:F12 without ITS (BL), 2ng/ml TGFβ1 was added and cells harvested at 0–120 min for total RNA isolation. Fold change in gene expression relative to GAPDH was calculated as 2-ΔΔCt. There is an error in the image for Fig 5. Please see the complete, corrected Fig 5 here.
Fig 5

Differential growth response of reverted DN and KC keratocytes to ITS and TGFβ1 in hyperglycemic and normoglycemic media.

Four individual DN and KC reverted keratocytes were placed in a) serum-free DMEM:F12, b) high glucose serum-free (HGSF) DMEM, and c) low glucose serum-free (LGSF) DMEM, each with ITS, TGFβ1 or both together and proliferation assessed over 7 days. The results shown are the mean ± SEM of 4 independent DN and KC primary stocks, with 3 technical replicates of each, at each time point. Significance was calculated using two-way Anova and multiple comparisons with * indicating p≤0.05.

Differential growth response of reverted DN and KC keratocytes to ITS and TGFβ1 in hyperglycemic and normoglycemic media.

Four individual DN and KC reverted keratocytes were placed in a) serum-free DMEM:F12, b) high glucose serum-free (HGSF) DMEM, and c) low glucose serum-free (LGSF) DMEM, each with ITS, TGFβ1 or both together and proliferation assessed over 7 days. The results shown are the mean ± SEM of 4 independent DN and KC primary stocks, with 3 technical replicates of each, at each time point. Significance was calculated using two-way Anova and multiple comparisons with * indicating p≤0.05.
  1 in total

1.  Transforming growth factor β and insulin signal changes in stromal fibroblasts of individual keratoconus patients.

Authors:  James Foster; Wai-Hong Wu; Sherri-Gae Scott; Mehak Bassi; Divya Mohan; Yassine Daoud; Walter J Stark; Albert S Jun; Shukti Chakravarti
Journal:  PLoS One       Date:  2014-09-23       Impact factor: 3.240

  1 in total

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