Altered placental ion channel gene expression in preeclamptic high-altitude pregnancies

High-altitude (>2,500 m) residence increases the risk of pregnancy vascular disorders such as fetal growth restriction and preeclampsia, each characterized by impaired placental function. Genetic attributes of highland ancestry confer relative protection against vascular disorders of pregnancy at...

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Veröffentlicht in:Physiological genomics 2023-09, Vol.55 (9), p.357-367
Hauptverfasser: Julian, Colleen G, Houck, Julie A, Fallahi, Sahand, Lazo-Vega, Litzi, Matarazzo, Christopher J, Diamond, Breea, Miranda-Garrido, Valquiria, Krause, Bernardo J, Moore, Lorna G, Shortt, Jonathan A, Toledo-Jaldin, Lilian, Lorca, Ramón A
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Sprache:eng
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Zusammenfassung:High-altitude (>2,500 m) residence increases the risk of pregnancy vascular disorders such as fetal growth restriction and preeclampsia, each characterized by impaired placental function. Genetic attributes of highland ancestry confer relative protection against vascular disorders of pregnancy at high altitudes. Although ion channels have been implicated in placental function regulation, neither their expression in high-altitude placentas nor their relationship to high-altitude preeclampsia has been determined. Here, we measured the expression of 26 ion-channel genes in placentas from preeclampsia cases and normotensive controls in La Paz, Bolivia (3,850 m). In addition, we correlated gene transcription to maternal and infant ancestry proportions. Gene expression was assessed by PCR, genetic ancestry evaluated by , and ion channel proteins localized by immunofluorescence. In preeclamptic placentas, 11 genes were downregulated ( , , , , , , , , , , and ) and two were upregulated ( and ). expression was positively correlated with high-altitude Amerindian ancestry and negatively correlated with non-high altitude. was negatively correlated with African ancestry, despite minimal African admixture. Most ion channels were localized in syncytiotrophoblasts (Cav1.2, TRPP2, TRPV6, and Kv7.1), whereas expression of Kv7.4 was primarily in microvillous membranes, Kir6.1 in chorionic plate and fetal vessels, and MinK in stromal cells. Our findings suggest a role for differential placental ion channel expression in the development of preeclampsia. Functional studies are needed to determine processes affected by these ion channels in the placenta and whether therapies directed at modulating their activity could influence the onset or severity of preeclampsia.
ISSN:1094-8341
1531-2267
1531-2267
DOI:10.1152/physiolgenomics.00013.2023