Intestinal proteome changes during infant necrotizing enterocolitis

Research output: Contribution to journalJournal articleResearchpeer-review

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Intestinal proteome changes during infant necrotizing enterocolitis. / Jiang, Pingping; Smith, Birgitte; Qvist, Niels; Nielsen, Christian; Wan, Jennifer Man-Fan; Sit, Wai-Hung; Jensen, Tim Kåre; Wang, Hualin; Sangild, Per Torp.

In: Pediatric Research, Vol. 73, No. 3, 2013, p. 268-276.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jiang, P, Smith, B, Qvist, N, Nielsen, C, Wan, JM-F, Sit, W-H, Jensen, TK, Wang, H & Sangild, PT 2013, 'Intestinal proteome changes during infant necrotizing enterocolitis', Pediatric Research, vol. 73, no. 3, pp. 268-276. https://doi.org/10.1038/pr.2012.182

APA

Jiang, P., Smith, B., Qvist, N., Nielsen, C., Wan, J. M-F., Sit, W-H., Jensen, T. K., Wang, H., & Sangild, P. T. (2013). Intestinal proteome changes during infant necrotizing enterocolitis. Pediatric Research, 73(3), 268-276. https://doi.org/10.1038/pr.2012.182

Vancouver

Jiang P, Smith B, Qvist N, Nielsen C, Wan JM-F, Sit W-H et al. Intestinal proteome changes during infant necrotizing enterocolitis. Pediatric Research. 2013;73(3):268-276. https://doi.org/10.1038/pr.2012.182

Author

Jiang, Pingping ; Smith, Birgitte ; Qvist, Niels ; Nielsen, Christian ; Wan, Jennifer Man-Fan ; Sit, Wai-Hung ; Jensen, Tim Kåre ; Wang, Hualin ; Sangild, Per Torp. / Intestinal proteome changes during infant necrotizing enterocolitis. In: Pediatric Research. 2013 ; Vol. 73, No. 3. pp. 268-276.

Bibtex

@article{d84b736665ec4929ab019f48bfecd6f4,
title = "Intestinal proteome changes during infant necrotizing enterocolitis",
abstract = "Background: Changes in the intestinal and colonic proteome in patients with necrotizing enterocolitis (NEC) may help to characterize the disease pathology and identify new biomarkers and treatment targets for NEC.Methods: Using gel-based proteomics, proteins in NEC-affected intestinal and colonic sections were compared with those in adjacent, near-normal tissue sections within the same patients. Western blot and immunohistochemistry were applied to crossvalidate proteomic data and histological location of some selected proteins.Results: Thirty proteins were identified with differential expression between necrotic and vital small-intestine sections and 23 proteins were identified for colon sections. Five proteins were similarly affected in the small intestine and colon: histamine receptors (HRs), actins, globins, immunoglobulin, and antitrypsin. Two heat shock proteins (HSPs) were affected in the small intestine. Furthermore, proteins involved in antioxidation, angiogenesis, cytoskeleton formation, and metabolism were affected. Finally, secretory proteins such as antitrypsin, fatty-acid binding protein 5, and haptoglobin differed between NEC-affected and vital tissues.Conclusion: NEC progression affects different pathways in the small intestine and colon. HSPs may play an important role, especially in the small intestine. The identified secretory proteins should be investigated as possible circulating markers of NEC progression in different gut regions.",
author = "Pingping Jiang and Birgitte Smith and Niels Qvist and Christian Nielsen and Wan, {Jennifer Man-Fan} and Wai-Hung Sit and Jensen, {Tim K{\aa}re} and Hualin Wang and Sangild, {Per Torp}",
note = "CURIS 2013 NEXS 029",
year = "2013",
doi = "10.1038/pr.2012.182",
language = "English",
volume = "73",
pages = "268--276",
journal = "Pediatric Research",
issn = "0031-3998",
publisher = "nature publishing group",
number = "3",

}

RIS

TY - JOUR

T1 - Intestinal proteome changes during infant necrotizing enterocolitis

AU - Jiang, Pingping

AU - Smith, Birgitte

AU - Qvist, Niels

AU - Nielsen, Christian

AU - Wan, Jennifer Man-Fan

AU - Sit, Wai-Hung

AU - Jensen, Tim Kåre

AU - Wang, Hualin

AU - Sangild, Per Torp

N1 - CURIS 2013 NEXS 029

PY - 2013

Y1 - 2013

N2 - Background: Changes in the intestinal and colonic proteome in patients with necrotizing enterocolitis (NEC) may help to characterize the disease pathology and identify new biomarkers and treatment targets for NEC.Methods: Using gel-based proteomics, proteins in NEC-affected intestinal and colonic sections were compared with those in adjacent, near-normal tissue sections within the same patients. Western blot and immunohistochemistry were applied to crossvalidate proteomic data and histological location of some selected proteins.Results: Thirty proteins were identified with differential expression between necrotic and vital small-intestine sections and 23 proteins were identified for colon sections. Five proteins were similarly affected in the small intestine and colon: histamine receptors (HRs), actins, globins, immunoglobulin, and antitrypsin. Two heat shock proteins (HSPs) were affected in the small intestine. Furthermore, proteins involved in antioxidation, angiogenesis, cytoskeleton formation, and metabolism were affected. Finally, secretory proteins such as antitrypsin, fatty-acid binding protein 5, and haptoglobin differed between NEC-affected and vital tissues.Conclusion: NEC progression affects different pathways in the small intestine and colon. HSPs may play an important role, especially in the small intestine. The identified secretory proteins should be investigated as possible circulating markers of NEC progression in different gut regions.

AB - Background: Changes in the intestinal and colonic proteome in patients with necrotizing enterocolitis (NEC) may help to characterize the disease pathology and identify new biomarkers and treatment targets for NEC.Methods: Using gel-based proteomics, proteins in NEC-affected intestinal and colonic sections were compared with those in adjacent, near-normal tissue sections within the same patients. Western blot and immunohistochemistry were applied to crossvalidate proteomic data and histological location of some selected proteins.Results: Thirty proteins were identified with differential expression between necrotic and vital small-intestine sections and 23 proteins were identified for colon sections. Five proteins were similarly affected in the small intestine and colon: histamine receptors (HRs), actins, globins, immunoglobulin, and antitrypsin. Two heat shock proteins (HSPs) were affected in the small intestine. Furthermore, proteins involved in antioxidation, angiogenesis, cytoskeleton formation, and metabolism were affected. Finally, secretory proteins such as antitrypsin, fatty-acid binding protein 5, and haptoglobin differed between NEC-affected and vital tissues.Conclusion: NEC progression affects different pathways in the small intestine and colon. HSPs may play an important role, especially in the small intestine. The identified secretory proteins should be investigated as possible circulating markers of NEC progression in different gut regions.

U2 - 10.1038/pr.2012.182

DO - 10.1038/pr.2012.182

M3 - Journal article

C2 - 23324825

VL - 73

SP - 268

EP - 276

JO - Pediatric Research

JF - Pediatric Research

SN - 0031-3998

IS - 3

ER -

ID: 44163105