Literature DB >> 29723064

Cell free hemoglobin in the fetoplacental circulation: a novel cause of fetal growth restriction?

Adam Brook1,2, Annie Hoaksey1,2, Rekha Gurung1,2, Edward E C Yoong1,2, Rosanna Sneyd1,2, Georgia C Baynes1,2, Helen Bischof1,2, Sarah Jones3, Lucy E Higgins1,2, Carolyn Jones1,2, Susan L Greenwood1,2, Rebecca L Jones1,2, Magnus Gram4, Ingrid Lang5, Gernot Desoye6, Jenny Myers1,2, Henning Schneider7, Stefan R Hansson8, Ian P Crocker1,2, Paul Brownbill1,2.   

Abstract

Cell free hemoglobin impairs vascular function and blood flow in adult cardiovascular disease. In this study, we investigated the hypothesis that free fetal hemoglobin (fHbF) compromises vascular integrity and function in the fetoplacental circulation, contributing to the increased vascular resistance associated with fetal growth restriction (FGR). Women with normal and FGR pregnancies were recruited and their placentas collected freshly postpartum. FGR fetal capillaries showed evidence of erythrocyte vascular packing and extravasation. Fetal cord blood fHbF levels were higher in FGR than in normal pregnancies ( P < 0.05) and the elevation of fHbF in relation to heme oxygenase-1 suggests a failure of expected catabolic compensation, which occurs in adults. During ex vivo placental perfusion, pathophysiological fHbF concentrations significantly increased fetal-side microcirculatory resistance ( P < 0.05). fHbF sequestered NO in acute and chronic exposure models ( P < 0.001), and fHbF-primed placental endothelial cells developed a proinflammatory phenotype, demonstrated by activation of NF-κB pathway, generation of IL-1α and TNF-α (both P < 0.05), uncontrolled angiogenesis, and disruption of endothelial cell flow alignment. Elevated fHbF contributes to increased fetoplacental vascular resistance and impaired endothelial protection. This unrecognized mechanism for fetal compromise offers a novel insight into FGR as well as a potential explanation for associated poor fetal outcomes such as fetal demise and stillbirth.-Brook, A., Hoaksey, A., Gurung, R., Yoong, E. E. C., Sneyd, R., Baynes, G. C., Bischof, H., Jones, S., Higgins, L. E., Jones, C., Greenwood, S. L., Jones, R. L., Gram, M., Lang, I., Desoye, G., Myers, J., Schneider, H., Hansson, S. R., Crocker, I. P., Brownbill, P. Cell free hemoglobin in the fetoplacental circulation: a novel cause of fetal growth restriction?

Entities:  

Keywords:  blood-flow resistance; endothelium; nitric oxide; stillbirth; vascular compromise

Mesh:

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Year:  2018        PMID: 29723064     DOI: 10.1096/fj.201800264R

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  3 in total

1.  Different morphological and gene expression profile in placentas of the same sickle cell anemia patient in pregnancies of opposite outcomes.

Authors:  Letícia C Baptista; Camilla O Figueira; Bruno B Souza; Kleber Y Fertrin; Arthur Antolini; Fernando F Costa; Mônica B de Melo; Maria Laura Costa
Journal:  Exp Biol Med (Maywood)       Date:  2019-02-28

2.  Longitudinal changes in plasma hemopexin and alpha-1-microglobulin concentrations in women with and without clinical risk factors for pre-eclampsia.

Authors:  Katja Murtoniemi; Grigorios Kalapotharakos; Tero Vahlberg; Katri Räikkonen; Eero Kajantie; Esa Hämäläinen; Bo Åkerström; Pia M Villa; Stefan R Hansson; Hannele Laivuori
Journal:  PLoS One       Date:  2019-12-16       Impact factor: 3.240

Review 3.  The Role of α1-Microglobulin (A1M) in Erythropoiesis and Erythrocyte Homeostasis-Therapeutic Opportunities in Hemolytic Conditions.

Authors:  Amanda Kristiansson; Magnus Gram; Johan Flygare; Stefan R Hansson; Bo Åkerström; Jill R Storry
Journal:  Int J Mol Sci       Date:  2020-09-30       Impact factor: 5.923

  3 in total

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