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1.
Biomaterials ; 192: 140-148, 2019 02.
Article in English | MEDLINE | ID: mdl-30448698

ABSTRACT

Fetal development may be compromised by adverse events at the placental interface between mother and fetus. However, it is still unclear how the communication between mother and fetus occurs through the placenta. In vitro - models of the human placental barrier, which could help our understanding and which recreate three-dimensional (3D) structures with biological functionalities and vasculatures, have not been reported yet. Here we present a 3D-vascularized human primary placental barrier model which can be constructed in 1 day. We illustrate the similarity of our model to first trimester human placenta, both in its structure and in its ability to respond to altered oxygen and to secrete factors that cause damage cells across the barrier including embryonic cortical neurons. We use this model to highlight the possibility that both the trophoblast and the endothelium within the placenta might play a role in the fetomaternal dialogue.


Subject(s)
Connective Tissue Cells/cytology , Endothelium, Vascular/cytology , Placenta/blood supply , Trophoblasts/cytology , Cells, Cultured , Female , Human Umbilical Vein Endothelial Cells , Humans , Neurons/cytology , Placenta/cytology , Pregnancy
2.
Eur J Hum Genet ; 19(5): 513-9, 2011 May.
Article in English | MEDLINE | ID: mdl-21368916

ABSTRACT

Bohring-Opitz syndrome (BOS) is a rare congenital disorder of unknown etiology diagnosed on the basis of distinctive clinical features. We suggest diagnostic criteria for this condition, describe ten previously unreported patients, and update the natural history of four previously reported patients. This is the largest series reported to date, providing a unique opportunity to document the key clinical features and course through childhood. Investigations undertaken to try and elucidate the underlying pathogenesis of BOS using array comparative genomic hybridization and tandem mass spectrometry of cholesterol precursors did not show any pathogenic changes responsible.


Subject(s)
Cholesterol/biosynthesis , Child, Preschool , Comparative Genomic Hybridization , Craniosynostoses/genetics , Craniosynostoses/pathology , Craniosynostoses/physiopathology , Female , Humans , Infant , Intellectual Disability/genetics , Intellectual Disability/pathology , Intellectual Disability/physiopathology , Male
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