Cargando…

Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature

The placental microvasculature is a conduit for fetal blood allowing solute exchange between the mother and the fetus. Serial block‐face scanning electron microscopy (SBF SEM) allows ultrastructure to be viewed in three dimensions and provides a new perspective on placental anatomy. This study used...

Descripción completa

Detalles Bibliográficos
Autores principales: Palaiologou, Eleni, Goggin, Patricia, Chatelet, David S., Ribeiro de Souza, Rodolfo, Chiu, Wendy, Ashley, Brogan, Lofthouse, Emma M., Sengers, Bram G., Torrens, Christopher, Page, Anton M., Cleal, Jane K., Lewis, Rohan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369196/
https://www.ncbi.nlm.nih.gov/pubmed/32242928
http://dx.doi.org/10.1111/joa.13191
_version_ 1783560743652687872
author Palaiologou, Eleni
Goggin, Patricia
Chatelet, David S.
Ribeiro de Souza, Rodolfo
Chiu, Wendy
Ashley, Brogan
Lofthouse, Emma M.
Sengers, Bram G.
Torrens, Christopher
Page, Anton M.
Cleal, Jane K.
Lewis, Rohan M.
author_facet Palaiologou, Eleni
Goggin, Patricia
Chatelet, David S.
Ribeiro de Souza, Rodolfo
Chiu, Wendy
Ashley, Brogan
Lofthouse, Emma M.
Sengers, Bram G.
Torrens, Christopher
Page, Anton M.
Cleal, Jane K.
Lewis, Rohan M.
author_sort Palaiologou, Eleni
collection PubMed
description The placental microvasculature is a conduit for fetal blood allowing solute exchange between the mother and the fetus. Serial block‐face scanning electron microscopy (SBF SEM) allows ultrastructure to be viewed in three dimensions and provides a new perspective on placental anatomy. This study used SBF SEM to study endothelial cells within the human placental microvasculature from uncomplicated pregnancies. Term human placental villi were aldehyde‐fixed and processed for imaging by SBF SEM. Manual segmentation was carried out on a terminal villous capillary and an intermediate villous arteriole and venule. Twenty‐seven SBF SEM stacks from terminal villi were analysed using stereological approaches to determine the volumes of microvascular components and the proportions of pericyte coverage. SBF SEM analysis of capillary endothelial cells revealed the presence of interendothelial protrusions (IEPs) originating from the donor cell at the endothelial junction and forming deep thin projections up to 7 μm into the adjacent endothelial cells. IEP density was estimated to be in the order of 35 million cm(–3) placental tissue. Pericytes cover 15% of the fetal capillary surface area in terminal villi. In comparison, the cytotrophoblast covered 24% of the syncytiotrophoblast basal membrane. A trans‐endothelial channel was observed in a region of the vasculo‐syncytial capillary. Pericyte coverage was extensive in both arteriole and venule. Three‐dimensional imaging of the placental microvasculature identified novel ultrastructural features and provided an insight into factors that may influence capillary permeability and placental function. We hypothesise that the IEPs may allow mechanosensing between adjacent endothelial cells to assist in the maintenance of vessel integrity. The numbers of endothelial junctions, the presence of trans‐endothelial channels and the extent of pericyte coverage all provide an insight into the factors determining capillary permeability.
format Online
Article
Text
id pubmed-7369196
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-73691962020-07-21 Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature Palaiologou, Eleni Goggin, Patricia Chatelet, David S. Ribeiro de Souza, Rodolfo Chiu, Wendy Ashley, Brogan Lofthouse, Emma M. Sengers, Bram G. Torrens, Christopher Page, Anton M. Cleal, Jane K. Lewis, Rohan M. J Anat Original Articles The placental microvasculature is a conduit for fetal blood allowing solute exchange between the mother and the fetus. Serial block‐face scanning electron microscopy (SBF SEM) allows ultrastructure to be viewed in three dimensions and provides a new perspective on placental anatomy. This study used SBF SEM to study endothelial cells within the human placental microvasculature from uncomplicated pregnancies. Term human placental villi were aldehyde‐fixed and processed for imaging by SBF SEM. Manual segmentation was carried out on a terminal villous capillary and an intermediate villous arteriole and venule. Twenty‐seven SBF SEM stacks from terminal villi were analysed using stereological approaches to determine the volumes of microvascular components and the proportions of pericyte coverage. SBF SEM analysis of capillary endothelial cells revealed the presence of interendothelial protrusions (IEPs) originating from the donor cell at the endothelial junction and forming deep thin projections up to 7 μm into the adjacent endothelial cells. IEP density was estimated to be in the order of 35 million cm(–3) placental tissue. Pericytes cover 15% of the fetal capillary surface area in terminal villi. In comparison, the cytotrophoblast covered 24% of the syncytiotrophoblast basal membrane. A trans‐endothelial channel was observed in a region of the vasculo‐syncytial capillary. Pericyte coverage was extensive in both arteriole and venule. Three‐dimensional imaging of the placental microvasculature identified novel ultrastructural features and provided an insight into factors that may influence capillary permeability and placental function. We hypothesise that the IEPs may allow mechanosensing between adjacent endothelial cells to assist in the maintenance of vessel integrity. The numbers of endothelial junctions, the presence of trans‐endothelial channels and the extent of pericyte coverage all provide an insight into the factors determining capillary permeability. John Wiley and Sons Inc. 2020-04-03 2020-08 /pmc/articles/PMC7369196/ /pubmed/32242928 http://dx.doi.org/10.1111/joa.13191 Text en © 2020 The Authors. Journal of Anatomy published by John Wiley & Sons Ltd on behalf of Anatomical Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Palaiologou, Eleni
Goggin, Patricia
Chatelet, David S.
Ribeiro de Souza, Rodolfo
Chiu, Wendy
Ashley, Brogan
Lofthouse, Emma M.
Sengers, Bram G.
Torrens, Christopher
Page, Anton M.
Cleal, Jane K.
Lewis, Rohan M.
Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature
title Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature
title_full Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature
title_fullStr Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature
title_full_unstemmed Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature
title_short Serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature
title_sort serial block‐face scanning electron microscopy reveals novel intercellular connections in human term placental microvasculature
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369196/
https://www.ncbi.nlm.nih.gov/pubmed/32242928
http://dx.doi.org/10.1111/joa.13191
work_keys_str_mv AT palaiologoueleni serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT gogginpatricia serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT chateletdavids serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT ribeirodesouzarodolfo serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT chiuwendy serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT ashleybrogan serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT lofthouseemmam serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT sengersbramg serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT torrenschristopher serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT pageantonm serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT clealjanek serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature
AT lewisrohanm serialblockfacescanningelectronmicroscopyrevealsnovelintercellularconnectionsinhumantermplacentalmicrovasculature