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Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis

Resident macrophages reside in all tissues throughout the body and play a central role in both tissue homeostasis and inflammation. Although the inner ear was once believed to be “immune-privileged,” recent studies have shown that macrophages are distributed in the cochlea and may play important rol...

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Autores principales: Kishimoto, Ippei, Okano, Takayuki, Nishimura, Koji, Motohashi, Tsutomu, Omori, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817595/
https://www.ncbi.nlm.nih.gov/pubmed/31695671
http://dx.doi.org/10.3389/fneur.2019.01115
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author Kishimoto, Ippei
Okano, Takayuki
Nishimura, Koji
Motohashi, Tsutomu
Omori, Koichi
author_facet Kishimoto, Ippei
Okano, Takayuki
Nishimura, Koji
Motohashi, Tsutomu
Omori, Koichi
author_sort Kishimoto, Ippei
collection PubMed
description Resident macrophages reside in all tissues throughout the body and play a central role in both tissue homeostasis and inflammation. Although the inner ear was once believed to be “immune-privileged,” recent studies have shown that macrophages are distributed in the cochlea and may play important roles in the immune system thereof. Resident macrophages have heterogeneous origins among tissues and throughout developmental stages. However, the origins of embryonic cochlear macrophages remain unknown. Here, we show that the early development of resident macrophages in the mouse cochlea depends on yolk sac hematopoiesis. Accordingly, our results found that macrophages emerging around the developing otocyst at E10.5 exhibited dynamic changes in distribution and in situ proliferative capacity during embryonic and neonatal stages. Cochlear examination in Csf1r-null mice revealed a substantial decrease in the number of Iba1-positive macrophages in the spiral ganglion and spiral ligament, whereas they were still observed in the cochlear mesenchyme or on the intraluminal surface of the perilymphatic space. Our results demonstrated that two subtypes of resident macrophages are present in the embryonic cochlea, one being Csf1r-dependent macrophages that originate from the yolk sac and the other being Csf1r-independent macrophages that appear to be derived from the fetal liver via systemic circulation. We consider the present study to be a starting point for elucidating the roles of embryonic cochlear resident macrophages. Furthermore, resident macrophages in the embryonic cochlea could be a novel target for the treatment of various inner ear disorders.
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spelling pubmed-68175952019-11-06 Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis Kishimoto, Ippei Okano, Takayuki Nishimura, Koji Motohashi, Tsutomu Omori, Koichi Front Neurol Neurology Resident macrophages reside in all tissues throughout the body and play a central role in both tissue homeostasis and inflammation. Although the inner ear was once believed to be “immune-privileged,” recent studies have shown that macrophages are distributed in the cochlea and may play important roles in the immune system thereof. Resident macrophages have heterogeneous origins among tissues and throughout developmental stages. However, the origins of embryonic cochlear macrophages remain unknown. Here, we show that the early development of resident macrophages in the mouse cochlea depends on yolk sac hematopoiesis. Accordingly, our results found that macrophages emerging around the developing otocyst at E10.5 exhibited dynamic changes in distribution and in situ proliferative capacity during embryonic and neonatal stages. Cochlear examination in Csf1r-null mice revealed a substantial decrease in the number of Iba1-positive macrophages in the spiral ganglion and spiral ligament, whereas they were still observed in the cochlear mesenchyme or on the intraluminal surface of the perilymphatic space. Our results demonstrated that two subtypes of resident macrophages are present in the embryonic cochlea, one being Csf1r-dependent macrophages that originate from the yolk sac and the other being Csf1r-independent macrophages that appear to be derived from the fetal liver via systemic circulation. We consider the present study to be a starting point for elucidating the roles of embryonic cochlear resident macrophages. Furthermore, resident macrophages in the embryonic cochlea could be a novel target for the treatment of various inner ear disorders. Frontiers Media S.A. 2019-10-22 /pmc/articles/PMC6817595/ /pubmed/31695671 http://dx.doi.org/10.3389/fneur.2019.01115 Text en Copyright © 2019 Kishimoto, Okano, Nishimura, Motohashi and Omori. 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 Neurology
Kishimoto, Ippei
Okano, Takayuki
Nishimura, Koji
Motohashi, Tsutomu
Omori, Koichi
Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis
title Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis
title_full Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis
title_fullStr Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis
title_full_unstemmed Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis
title_short Early Development of Resident Macrophages in the Mouse Cochlea Depends on Yolk Sac Hematopoiesis
title_sort early development of resident macrophages in the mouse cochlea depends on yolk sac hematopoiesis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817595/
https://www.ncbi.nlm.nih.gov/pubmed/31695671
http://dx.doi.org/10.3389/fneur.2019.01115
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