Abstract:
:Exocytosis and endocytosis are the way of macromolecules transmembrane transport. Pulmonary surfactant (PS), one of such macromolecules, is secreted via exocytosis of lamellar bodies and recycled via endocytosis by type II alveolar epithelial cells (AEC II). It maintains low alveolar surface tension and is therefore essential to normal lung function. PS deficiency causes respiratory distress syndrome in infants. Congenital diaphragmatic hernia is an abnormal condition in which low lung compliance is involved. This condition is multifactorial and a primary surfactant deficiency may be responsible for it. We hypothesize that surfactant deficiency is involved in CDH and depressed activity of exocytosis and endocytosis in AEC II is responsible for the surfactant deficiency in the lung of newborn with congenital diaphragmatic hernia.
journal_name
Med Hypothesesjournal_title
Medical hypothesesauthors
Xu C,Liu W,Wang Y,Chen Z,Ji Ydoi
10.1016/j.mehy.2008.09.012subject
Has Abstractpub_date
2009-02-01 00:00:00pages
160-2issue
2eissn
0306-9877issn
1532-2777pii
S0306-9877(08)00460-Xjournal_volume
72pub_type
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journal_title:Medical hypotheses
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pub_type: 杂志文章
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更新日期:2015-11-01 00:00:00
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pub_type: 杂志文章
doi:10.1016/j.mehy.2006.06.001
更新日期:2006-01-01 00:00:00
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doi:10.1016/j.mehy.2013.06.012
更新日期:2013-09-01 00:00:00
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pub_type: 杂志文章
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pub_type: 杂志文章
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pub_type: 杂志文章
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pub_type: 杂志文章
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journal_title:Medical hypotheses
pub_type: 杂志文章
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更新日期:2017-09-01 00:00:00
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journal_title:Medical hypotheses
pub_type: 杂志文章
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journal_title:Medical hypotheses
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