Placental Vacuolar ATPase Function Is a Key Link between Multiple Causes of Preeclampsia

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Placental Vacuolar ATPase Function Is a Key Link between Multiple Causes of Preeclampsia

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Title: Placental Vacuolar ATPase Function Is a Key Link between Multiple Causes of Preeclampsia
Author: Zhang, Dongxin; Ye, Duyun; Chen, Hongxiang

Note: Order does not necessarily reflect citation order of authors.

Citation: Zhang, Dongxin, Duyun Ye, and Hongxiang Chen. 2013. “Placental Vacuolar ATPase Function Is a Key Link between Multiple Causes of Preeclampsia.” ISRN Obstetrics and Gynecology 2013 (1): 504173. doi:10.1155/2013/504173. http://dx.doi.org/10.1155/2013/504173.
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Abstract: Preeclampsia, a relatively common pregnancy disorder, is one of the major causes of maternal and fetal morbidity and mortality. Despite numerous research, the etiology of this syndrome remains not well understood as the pathogenesis of preeclampsia is complex, involving interaction between genetic, immunologic, and environmental factors. Preeclampsia, originating in placenta abnormalities, is induced by the circulating factors derived from the abnormal placenta. Recent work has identified various molecular mechanisms related to placenta development, including renin-angiotensin system, 1, 25-dihydroxyvitamin D, and lipoxin A4. Interestingly, advances suggest that vacuolar ATPase, a key molecule in placentation, is closely associated with them. Therefore, this intriguing molecule may represent an important link between various causes of preeclampsia. Here, we review that vacuolar ATPase works as a key link between multiple causes of preeclampsia and discuss the potential molecular mechanisms. The novel findings outlined in this review may provide promising explanations for the causation of preeclampsia and a rationale for future therapeutic interventions for this condition.
Published Version: doi:10.1155/2013/504173
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674723/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11708669
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