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The human splenic microcirculation is entirely open as shown by 3D models in virtual reality
The human spleen is equipped with an organ-specific microcirculation. The initial part of the venous circulation is formed by spleen-specific large microvessels, the sinuses. Sinuses eventually fuse to form venules and veins. For more than 170 years there have been debates, whether splenic red pulp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526706/ https://www.ncbi.nlm.nih.gov/pubmed/36182999 http://dx.doi.org/10.1038/s41598-022-19885-z |
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author | Steiniger, Birte S. Pfeffer, Henriette Gaffling, Simone Lobachev, Oleg |
author_facet | Steiniger, Birte S. Pfeffer, Henriette Gaffling, Simone Lobachev, Oleg |
author_sort | Steiniger, Birte S. |
collection | PubMed |
description | The human spleen is equipped with an organ-specific microcirculation. The initial part of the venous circulation is formed by spleen-specific large microvessels, the sinuses. Sinuses eventually fuse to form venules and veins. For more than 170 years there have been debates, whether splenic red pulp capillaries join sinuses, i.e., whether the microcirculation is closed or open—or even simultaneously closed and open. We have now solved this question by three-dimensional reconstruction of a limited number of immunostained serial sections of red and white pulp areas, which were visualized in virtual reality. Splenic capillaries have special end structures exhibiting multiple small diverging endothelial cell processes, which always keep a certain distance to the walls of sinuses. Only very few capillary ends were difficult to diagnose. Positive identification of these end structures permits to conclude that the human splenic microcirculation is entirely open. This is also true for the perifollicular capillary network and for capillaries close to red pulp venules. Follicles are supplied by a relatively dense open perifollicular capillary net, which is primarily, but not exclusively, fed by sheathed and few non-sheathed capillaries from the surrounding red pulp network. |
format | Online Article Text |
id | pubmed-9526706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95267062022-10-03 The human splenic microcirculation is entirely open as shown by 3D models in virtual reality Steiniger, Birte S. Pfeffer, Henriette Gaffling, Simone Lobachev, Oleg Sci Rep Article The human spleen is equipped with an organ-specific microcirculation. The initial part of the venous circulation is formed by spleen-specific large microvessels, the sinuses. Sinuses eventually fuse to form venules and veins. For more than 170 years there have been debates, whether splenic red pulp capillaries join sinuses, i.e., whether the microcirculation is closed or open—or even simultaneously closed and open. We have now solved this question by three-dimensional reconstruction of a limited number of immunostained serial sections of red and white pulp areas, which were visualized in virtual reality. Splenic capillaries have special end structures exhibiting multiple small diverging endothelial cell processes, which always keep a certain distance to the walls of sinuses. Only very few capillary ends were difficult to diagnose. Positive identification of these end structures permits to conclude that the human splenic microcirculation is entirely open. This is also true for the perifollicular capillary network and for capillaries close to red pulp venules. Follicles are supplied by a relatively dense open perifollicular capillary net, which is primarily, but not exclusively, fed by sheathed and few non-sheathed capillaries from the surrounding red pulp network. Nature Publishing Group UK 2022-10-01 /pmc/articles/PMC9526706/ /pubmed/36182999 http://dx.doi.org/10.1038/s41598-022-19885-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Steiniger, Birte S. Pfeffer, Henriette Gaffling, Simone Lobachev, Oleg The human splenic microcirculation is entirely open as shown by 3D models in virtual reality |
title | The human splenic microcirculation is entirely open as shown by 3D models in virtual reality |
title_full | The human splenic microcirculation is entirely open as shown by 3D models in virtual reality |
title_fullStr | The human splenic microcirculation is entirely open as shown by 3D models in virtual reality |
title_full_unstemmed | The human splenic microcirculation is entirely open as shown by 3D models in virtual reality |
title_short | The human splenic microcirculation is entirely open as shown by 3D models in virtual reality |
title_sort | human splenic microcirculation is entirely open as shown by 3d models in virtual reality |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526706/ https://www.ncbi.nlm.nih.gov/pubmed/36182999 http://dx.doi.org/10.1038/s41598-022-19885-z |
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