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PPAR Research
Volume 2010 (2010), Article ID 627284, 2 pages
http://dx.doi.org/10.1155/2010/627284
Erratum

Erratum to “Peroxisome Proliferator-Activated Receptors Alpha, Beta, and Gamma mRNA and Protein Expression in Human Fetal Tissues”

Toxicity Assessment Division, Developmental Toxicology Branch, National Health and Environmental Effects Research Laboratory, (MD-67) Office of Research and Development, US Environmental Protection Agency, Research Triangle Park, NC 27711, USA

Received 31 December 2010; Accepted 31 December 2010

Copyright © 2010 Barbara D. Abbott et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


In the above-mentioned paper, the expression of PPARγ was incorrectly determined based on the quantification of a 50 kD band on the Western blots. This band aligned with what was believed to be a positive control band in the U937 whole cell extract, a control reagent recommended by the supplier of the primary antibody, SC-7196 (Santa Cruz Biotechnologies, Santa Cruz, CA). Based on recent information described by Foreman et al. [1], it is clear that this band is not PPARγ but was a nonspecific immunoreactive protein detected by SC-7196. This nonspecific protein was abundantly detected by SC-7196 in U937 and COS-1 cells as well as across all human fetal protein samples. Immunoprecipitation of COS-1 cell lysate using agarose-conjugated SC-7196 resulted in a single band on a Coomassie Blue-stained gel. This band was subjected to digestion, peptide extraction, and sequence analysis using MALDI-MSMS, and the protein was identified as cytoplasmic actin with a decisive score (human SwissProt database, 60% protein coverage using the 15 highest scoring peptide groups and two lower scoring but acceptable peptides).

A specific band for PPARγ, (calculated molecular weight for human PPARγ1 = 54.55 kD) was identified on our Western blots by performing new experiments in which in vitro translated human PPARγ1 (provided by J. Peters, Pennsylvania State University) was compared with human fetal tissue lysates (Figure 1). These experiments also included COS-1 cell lysate as a negative control and U937 cell lysate. The Western blots of the fetal tissues were all reanalyzed using the ~55 kD band that aligned with the in vitro translated human PPARγ1. Based on this reanalysis, the expression of PPARγ protein shown in (c) of Figures  1–9 are replaced by Figure 2. The data summary described in Table  1 of the above-mentioned paper regarding the change in PPARγ protein expression with fetal age is replaced by Table 1.

tab1
Table 1
627284.fig.001
Figure 1: Western blot showing the comparison of banding patterns in COS-1 cell lysate, U937 cell lysate, in vitro translated human PPARγ1, and tissue lysate from human fetal stomach samples. The ~55 kD band of human PPARγ1 and corresponding band in stomach tissue lysate is marked with an asterisk (*). The nonspecific, cytoplasmic actin band is marked with an arrow.
fig2
Figure 2: PPARγ protein expression is shown across the fetal age range for each tissue. Western blot density normalized to glyceraldehyde-3-phophate dehydrogenase (GAPDH). If only one sample was available for a particular age, then an error term could not be calculated and no SEM bar is shown. Regression analysis evaluated change with age. Dashed lines are the 95% confidence interval.

The authors regret this unexpected error. The clarification of the recognition patterns of this primary antibody should be of value to investigators interested in detecting PPARγ protein.

References

  1. J. E. Foreman, J. M. Sorg, K. S. McGinnis, et al., “Erratum: to Regulation of peroxisome proliferator-activated receptor-β/δ by the APC/β-CATENIN pathway and nonsteroidal antiinflammatory drugs,” Molecular Carcinogenesis, in press. View at Publisher · View at Google Scholar