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Telocytes: a potential defender in the spleen of Npc1 mutant mice
Niemann–Pick disease, type C1 (Npc1), is an atypical lysosomal storage disorder caused by autosomal recessive inheritance of mutations in Npc1 gene. In the Npc1 mutant mice (Npc1(−/−)), the initial manifestation is enlarged spleen, concomitant with free cholesterol accumulation. Telocytes (TCs), a n...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387173/ https://www.ncbi.nlm.nih.gov/pubmed/27860245 http://dx.doi.org/10.1111/jcmm.13024 |
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author | Zhang, Bichao Yang, Ciqing Qiao, Liang Li, Qiuling Wang, Congrui Yan, Xin Lin, Juntang |
author_facet | Zhang, Bichao Yang, Ciqing Qiao, Liang Li, Qiuling Wang, Congrui Yan, Xin Lin, Juntang |
author_sort | Zhang, Bichao |
collection | PubMed |
description | Niemann–Pick disease, type C1 (Npc1), is an atypical lysosomal storage disorder caused by autosomal recessive inheritance of mutations in Npc1 gene. In the Npc1 mutant mice (Npc1(−/−)), the initial manifestation is enlarged spleen, concomitant with free cholesterol accumulation. Telocytes (TCs), a novel type of interstitial cell, exist in a variety of tissues including spleen, presumably thought to be involved in many biological processes such as nursing stem cells and recruiting inflammatory cells. In this study, we found that the spleen is significantly enlarged in Npc1(−/−) mice, and the results from transmission electron microscopy examination and immunostaining using three different TCs markers, c‐Kit, CD34 and Vimentin revealed significantly increased splenic TCs in Npc1(−/−) mice. Furthermore, hematopoietic stem cells and macrophages were also elevated in Npc1(−/−) spleen. Taken together, our data indicate that splenic TCs might alleviate the progress of splenic malfunction via recruiting hematopoietic stem cells and macrophages. |
format | Online Article Text |
id | pubmed-5387173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53871732017-05-01 Telocytes: a potential defender in the spleen of Npc1 mutant mice Zhang, Bichao Yang, Ciqing Qiao, Liang Li, Qiuling Wang, Congrui Yan, Xin Lin, Juntang J Cell Mol Med Original Articles Niemann–Pick disease, type C1 (Npc1), is an atypical lysosomal storage disorder caused by autosomal recessive inheritance of mutations in Npc1 gene. In the Npc1 mutant mice (Npc1(−/−)), the initial manifestation is enlarged spleen, concomitant with free cholesterol accumulation. Telocytes (TCs), a novel type of interstitial cell, exist in a variety of tissues including spleen, presumably thought to be involved in many biological processes such as nursing stem cells and recruiting inflammatory cells. In this study, we found that the spleen is significantly enlarged in Npc1(−/−) mice, and the results from transmission electron microscopy examination and immunostaining using three different TCs markers, c‐Kit, CD34 and Vimentin revealed significantly increased splenic TCs in Npc1(−/−) mice. Furthermore, hematopoietic stem cells and macrophages were also elevated in Npc1(−/−) spleen. Taken together, our data indicate that splenic TCs might alleviate the progress of splenic malfunction via recruiting hematopoietic stem cells and macrophages. John Wiley and Sons Inc. 2016-11-18 2017-05 /pmc/articles/PMC5387173/ /pubmed/27860245 http://dx.doi.org/10.1111/jcmm.13024 Text en © 2016 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (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 Zhang, Bichao Yang, Ciqing Qiao, Liang Li, Qiuling Wang, Congrui Yan, Xin Lin, Juntang Telocytes: a potential defender in the spleen of Npc1 mutant mice |
title | Telocytes: a potential defender in the spleen of Npc1 mutant mice |
title_full | Telocytes: a potential defender in the spleen of Npc1 mutant mice |
title_fullStr | Telocytes: a potential defender in the spleen of Npc1 mutant mice |
title_full_unstemmed | Telocytes: a potential defender in the spleen of Npc1 mutant mice |
title_short | Telocytes: a potential defender in the spleen of Npc1 mutant mice |
title_sort | telocytes: a potential defender in the spleen of npc1 mutant mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387173/ https://www.ncbi.nlm.nih.gov/pubmed/27860245 http://dx.doi.org/10.1111/jcmm.13024 |
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