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Correction: Maturation of the Intestinal Epithelial Barrier in Neonatal Rats Coincides with Decreased FcRn Expression, Replacement of Vacuolated Enterocytes and Changed Blimp-1 Expression.

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CORRECTION

Correction: Maturation of the Intestinal

Epithelial Barrier in Neonatal Rats Coincides

with Decreased FcRn Expression,

Replacement of Vacuolated Enterocytes and

Changed Blimp-1 Expression

Ester Are´valo Sureda, Bjo

¨ rn Westro

¨ m, Stefan G. Pierzynowski, Olena Prykhodko

The images for Figs

6

,

7

and

8

are incorrectly switched. The image that appears as

Fig 6

should

be

Fig 7

, the image that appears as

Fig 7

should be

Fig 8

, and the image that appears as

Fig 8

should be

Fig 6

. The figure captions appear in the correct order.

PLOS ONE | DOI:10.1371/journal.pone.0169724 January 3, 2017 1 / 4

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OPEN ACCESS

Citation: Are´valo Sureda E, Westro¨m B,

Pierzynowski SG, Prykhodko O (2017) Correction: Maturation of the Intestinal Epithelial Barrier in Neonatal Rats Coincides with Decreased FcRn Expression, Replacement of Vacuolated Enterocytes and Changed Blimp-1 Expression. PLoS ONE 12(1): e0169724. doi:10.1371/journal. pone.0169724

Published: January 3, 2017

Copyright:© 2017 Are´valo Sureda et al. This is an open access article distributed under the terms of theCreative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 6. Expression of mRNA for Fcgrt (FcRn) and Prdm1 (Blimp-1) in the SI of developing rats. Relative mRNA levels of Fcgrt (a, c) and Prdm1 (b, d) in the proximal and distal SI in 7, 14, 21, 28 and 35 days old rats (n = 4–6) during postnatal development (a, b) and in 17 days old rats treated with PHA or protease at 14–16 days of age (n = 3–4) to induce precocious gut maturation, compared to control rats (c, d). (mean±SD, a–b and*p<0.05;***p<0.001).

doi:10.1371/journal.pone.0169724.g001

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Fig 7. Plasma IgG as an accumulative marker for intestinal macromolecular permeability. (a) Changes in plasma IgG levels (mg/ml) during postnatal development in suckling rats, 7, 14, and 21 days old and post-weaning rats, 28, 35, 42, 49 and 56 days old (mean±SD, 10–90% percentile, (boxes), n = 6–10). (b) Decreased plasma IgG levels (mean±SD, n = 6) in 17 days old rats treated with PHA (*p<0.05) or protease (non-significant) during 3 days to induce precocious maturation, compared to control rats.

doi:10.1371/journal.pone.0169724.g002

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Reference

1. Are´valo Sureda E, Westro¨m B, Pierzynowski SG, Prykhodko O (2016) Maturation of the Intestinal Epi-thelial Barrier in Neonatal Rats Coincides with Decreased FcRn Expression, Replacement of Vacuo-lated Enterocytes and Changed Blimp-1 Expression. PLoS ONE 11(10): e0164775. doi:10.1371/ journal.pone.0164775PMID:27736989

Fig 8. Expression of Blimp-1 in the small intestine during suckling and post-weaning periods. Immunohistochemical staining of Blimp-1 in representative histological sections (magnification 200x) from the proximal and distal SI in suckling (14d) and post-weaning (28d) rats. Note: Nuclear immunorreactivity of Blimp-1 antibodies in epithelial cells indicated by black arrows; intraepithelial and lamina propria cells–red arrows; crypt cells–green arrows and cells in muscle layer are indicated by blue arrows.

doi:10.1371/journal.pone.0169724.g003

Figure

Fig 6. Expression of mRNA for Fcgrt (FcRn) and Prdm1 (Blimp-1) in the SI of developing rats
Fig 7. Plasma IgG as an accumulative marker for intestinal macromolecular permeability
Fig 8. Expression of Blimp-1 in the small intestine during suckling and post-weaning periods.

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