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High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow

Hematopoiesis is hosted, supported and regulated by a special bone marrow (BM) microenvironment known as “niche.” BM niches have been classified based on micro-anatomic distance from the bone surface into “endosteal” and “central” niches. Whilst different blood vessels have been found in both BM nic...

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Autores principales: Panvini, Francesca M., Pacini, Simone, Montali, Marina, Barachini, Serena, Mazzoni, Stefano, Morganti, Riccardo, Ciancia, Eugenio M., Carnicelli, Vittoria, Petrini, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753038/
https://www.ncbi.nlm.nih.gov/pubmed/33364234
http://dx.doi.org/10.3389/fcell.2020.596452
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author Panvini, Francesca M.
Pacini, Simone
Montali, Marina
Barachini, Serena
Mazzoni, Stefano
Morganti, Riccardo
Ciancia, Eugenio M.
Carnicelli, Vittoria
Petrini, Mario
author_facet Panvini, Francesca M.
Pacini, Simone
Montali, Marina
Barachini, Serena
Mazzoni, Stefano
Morganti, Riccardo
Ciancia, Eugenio M.
Carnicelli, Vittoria
Petrini, Mario
author_sort Panvini, Francesca M.
collection PubMed
description Hematopoiesis is hosted, supported and regulated by a special bone marrow (BM) microenvironment known as “niche.” BM niches have been classified based on micro-anatomic distance from the bone surface into “endosteal” and “central” niches. Whilst different blood vessels have been found in both BM niches in mice, our knowledge of the human BM architecture is much more limited. Here, we have used a combination of markers including NESTIN, CD146, and αSMA labeling different blood vessels in benign human BM. Applying immunohistochemical/immunofluorescence techniques on BM trephines and performing image analysis on almost 300 microphotographs, we detected high NESTIN expression in BM endothelial cells (BMECs) of small arteries (A) and endosteal arterioles (EA), and also in very small vessels we named NESTIN(+) capillary-like tubes (NCLTs), not surrounded by sub-endothelial perivascular cells that occasionally reported low levels of NESTIN expression. Statistically, NCLTs were detected within 40 μm from bone trabecula, frequently found in direct contact to the bone line and spatially correlated with hematopoietic stem/progenitor cells. Our results support the expression of NESTIN in human BMECs of EA and A in accordance with the updated classification of murine BM micro-vessels. NCLTs for their peculiar characteristics and micro-anatomical localization have been here proposed as transitional vessels possibly involved in regulating human hematopoiesis.
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spelling pubmed-77530382020-12-23 High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow Panvini, Francesca M. Pacini, Simone Montali, Marina Barachini, Serena Mazzoni, Stefano Morganti, Riccardo Ciancia, Eugenio M. Carnicelli, Vittoria Petrini, Mario Front Cell Dev Biol Cell and Developmental Biology Hematopoiesis is hosted, supported and regulated by a special bone marrow (BM) microenvironment known as “niche.” BM niches have been classified based on micro-anatomic distance from the bone surface into “endosteal” and “central” niches. Whilst different blood vessels have been found in both BM niches in mice, our knowledge of the human BM architecture is much more limited. Here, we have used a combination of markers including NESTIN, CD146, and αSMA labeling different blood vessels in benign human BM. Applying immunohistochemical/immunofluorescence techniques on BM trephines and performing image analysis on almost 300 microphotographs, we detected high NESTIN expression in BM endothelial cells (BMECs) of small arteries (A) and endosteal arterioles (EA), and also in very small vessels we named NESTIN(+) capillary-like tubes (NCLTs), not surrounded by sub-endothelial perivascular cells that occasionally reported low levels of NESTIN expression. Statistically, NCLTs were detected within 40 μm from bone trabecula, frequently found in direct contact to the bone line and spatially correlated with hematopoietic stem/progenitor cells. Our results support the expression of NESTIN in human BMECs of EA and A in accordance with the updated classification of murine BM micro-vessels. NCLTs for their peculiar characteristics and micro-anatomical localization have been here proposed as transitional vessels possibly involved in regulating human hematopoiesis. Frontiers Media S.A. 2020-12-08 /pmc/articles/PMC7753038/ /pubmed/33364234 http://dx.doi.org/10.3389/fcell.2020.596452 Text en Copyright © 2020 Panvini, Pacini, Montali, Barachini, Mazzoni, Morganti, Ciancia, Carnicelli and Petrini. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Panvini, Francesca M.
Pacini, Simone
Montali, Marina
Barachini, Serena
Mazzoni, Stefano
Morganti, Riccardo
Ciancia, Eugenio M.
Carnicelli, Vittoria
Petrini, Mario
High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow
title High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow
title_full High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow
title_fullStr High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow
title_full_unstemmed High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow
title_short High NESTIN Expression Marks the Endosteal Capillary Network in Human Bone Marrow
title_sort high nestin expression marks the endosteal capillary network in human bone marrow
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753038/
https://www.ncbi.nlm.nih.gov/pubmed/33364234
http://dx.doi.org/10.3389/fcell.2020.596452
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