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Citations to this article

Pass the bicarb: the importance of HCO3– for mucin release
Robert C. De Lisle
Robert C. De Lisle
Published August 24, 2009
Citation Information: J Clin Invest. 2009;119(9):2535-2537. https://doi.org/10.1172/JCI40598.
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Commentary Article has an altmetric score of 3

Pass the bicarb: the importance of HCO3– for mucin release

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Abstract

Accumulation of thick, sticky mucus is a hallmark of the genetic disease cystic fibrosis (CF) and has a central role in CF pathophysiology. Mutations in the CF transmembrane regulator (CFTR) ion channel are known to result in abnormally thick and sticky mucus; however, why mucus accumulates in CF is still not completely understood. In this issue of the JCI, Garcia and colleagues show that mucin — the heavily glycosylated protein contained within mucus — requires CFTR and bicarbonate in order to be released from mouse intestine (see the related article beginning on page 2613). The authors propose a model whereby CFTR-mediated bicarbonate secretion must be concurrent with mucin exocytosis for proper mucin release.

Authors

Robert C. De Lisle

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Total citations by year

Year: 2021 2015 2013 2011 2010 Total
Citations: 2 3 2 2 1 10
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article (10)

Title and authors Publication Year
Exploring the impact of intestinal ion transport on the gut microbiota
AC Engevik, MA Engevik
Computational and Structural Biotechnology Journal 2021
Chronic Inflammation in Ulcerative Colitis Causes Long-Term Changes in Goblet Cell Function
Singh V, Johnson K, Yin J, Lee S, Lin R, Yu H, In J, Foulke-Abel J, Zachos NC, Donowitz M, Rong Y
Cellular and Molecular Gastroenterology and Hepatology 2021
Clinical Presentations of Cystic Fibrosis in Iranian Children
F Motamed, M Moayednia, N Moayednia, MN Sani, F Farahmand, A Khodadad, G Fallahi
IRAN J PEDIATR 2015
5’-adenosine monophosphate mediated cooling treatment enhances ΔF508-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) stability in vivo
Y Zhang, WG OBrien, Z Zhao, CC Lee
Journal of Biomedical Science 2015
Evidence for a Cystic Fibrosis Enteropathy
MP Adriaanse, LJ van der Sande, AM van Neucker, PP Menheere, E Dompeling, WA Buurman, AC Vreugdenhil, N Palaniyar
PloS one 2015
Lineage-Specific Expression of Bestrophin-2 and Bestrophin-4 in Human Intestinal Epithelial Cells
G Ito, R Okamoto, T Murano, H Shimizu, S Fujii, T Nakata, T Mizutani, S Yui, J Akiyama-Morio, Y Nemoto, E Okada, A Araki, K Ohtsuka, K Tsuchiya, T Nakamura, M Watanabe, MJ Boucher
PloS one 2013
The Cystic Fibrosis of Exocrine Pancreas
M Wilschanski, I Novak
Cold Spring Harbor Perspectives in Medicine 2013
The role of female hormones on lung function in chronic lung diseases
A Tam, D Morrish, S Wadsworth, D Dorscheid, SF Man, DD Sin
BMC Women's Health 2011
Embryonic frog epidermis: a model for the study of cell-cell interactions in the development of mucociliary disease
E Dubaissi, N Papalopulu
Disease models & mechanisms 2011
A new role for bicarbonate secretion in cervico-uterine mucus release
RW Muchekehu, PM Quinton
The Journal of Physiology 2010

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