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CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis

Ecotropic viral integration site-1 (EVI1) has a critical role in normal and malignant hematopoiesis. Since we previously identified high expression of calcitonin receptor like receptor (CRLR) in acute myeloid leukemia (AML) with high EVI1 expression, we here characterized the function of CRLR in hem...

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Autores principales: Suekane, Akira, Saito, Yusuke, Nakahata, Shingo, Ichikawa, Tomonaga, Ogoh, Honami, Tsujikawa, Kazutake, Morishita, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344543/
https://www.ncbi.nlm.nih.gov/pubmed/30674976
http://dx.doi.org/10.1038/s41598-018-36796-0
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author Suekane, Akira
Saito, Yusuke
Nakahata, Shingo
Ichikawa, Tomonaga
Ogoh, Honami
Tsujikawa, Kazutake
Morishita, Kazuhiro
author_facet Suekane, Akira
Saito, Yusuke
Nakahata, Shingo
Ichikawa, Tomonaga
Ogoh, Honami
Tsujikawa, Kazutake
Morishita, Kazuhiro
author_sort Suekane, Akira
collection PubMed
description Ecotropic viral integration site-1 (EVI1) has a critical role in normal and malignant hematopoiesis. Since we previously identified high expression of calcitonin receptor like receptor (CRLR) in acute myeloid leukemia (AML) with high EVI1 expression, we here characterized the function of CRLR in hematopoiesis. Since higher expression of CRLR and receptor activity modifying protein 1 (RAMP1) was identified in immature hematopoietic bone marrow (BM) cells, we focused on calcitonin gene-related peptide (CGRP), a specific ligand for the CRLR/RAMP1 complex. To elucidate the role of CGRP in hematopoiesis, Ramp1-deficient (Ramp1(−/−)) mice were used. The steady-state hematopoiesis was almost maintained in Ramp1(−/−) mice; however, the BM repopulation capacity of Ramp1(−/−) mice was significantly decreased, and the transplanted Ramp1(−/−) BM mononuclear cells had low proliferation capacity with enhanced reactive oxygen species (ROS) production and cell apoptosis. Thus, CGRP is important for maintaining hematopoiesis during temporal exposures with proliferative stress. Moreover, continuous CGRP exposure to mice for two weeks induced a reduction in the number of BM immature hematopoietic cells along with differentiated myeloid cells. Since CGRP is known to be increased under inflammatory conditions to regulate immune responses, hematopoietic exhaustion by continuous CGRP secretion under chronic inflammatory conditions is probably one of the important mechanisms of anti-inflammatory responses.
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spelling pubmed-63445432019-01-28 CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis Suekane, Akira Saito, Yusuke Nakahata, Shingo Ichikawa, Tomonaga Ogoh, Honami Tsujikawa, Kazutake Morishita, Kazuhiro Sci Rep Article Ecotropic viral integration site-1 (EVI1) has a critical role in normal and malignant hematopoiesis. Since we previously identified high expression of calcitonin receptor like receptor (CRLR) in acute myeloid leukemia (AML) with high EVI1 expression, we here characterized the function of CRLR in hematopoiesis. Since higher expression of CRLR and receptor activity modifying protein 1 (RAMP1) was identified in immature hematopoietic bone marrow (BM) cells, we focused on calcitonin gene-related peptide (CGRP), a specific ligand for the CRLR/RAMP1 complex. To elucidate the role of CGRP in hematopoiesis, Ramp1-deficient (Ramp1(−/−)) mice were used. The steady-state hematopoiesis was almost maintained in Ramp1(−/−) mice; however, the BM repopulation capacity of Ramp1(−/−) mice was significantly decreased, and the transplanted Ramp1(−/−) BM mononuclear cells had low proliferation capacity with enhanced reactive oxygen species (ROS) production and cell apoptosis. Thus, CGRP is important for maintaining hematopoiesis during temporal exposures with proliferative stress. Moreover, continuous CGRP exposure to mice for two weeks induced a reduction in the number of BM immature hematopoietic cells along with differentiated myeloid cells. Since CGRP is known to be increased under inflammatory conditions to regulate immune responses, hematopoietic exhaustion by continuous CGRP secretion under chronic inflammatory conditions is probably one of the important mechanisms of anti-inflammatory responses. Nature Publishing Group UK 2019-01-23 /pmc/articles/PMC6344543/ /pubmed/30674976 http://dx.doi.org/10.1038/s41598-018-36796-0 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Suekane, Akira
Saito, Yusuke
Nakahata, Shingo
Ichikawa, Tomonaga
Ogoh, Honami
Tsujikawa, Kazutake
Morishita, Kazuhiro
CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis
title CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis
title_full CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis
title_fullStr CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis
title_full_unstemmed CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis
title_short CGRP-CRLR/RAMP1 signal is important for stress-induced hematopoiesis
title_sort cgrp-crlr/ramp1 signal is important for stress-induced hematopoiesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344543/
https://www.ncbi.nlm.nih.gov/pubmed/30674976
http://dx.doi.org/10.1038/s41598-018-36796-0
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