Cargando…

Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma

Bone pain is a serious and debilitating symptom of multiple myeloma (MM) that impairs the quality of life of patients. The underlying mechanisms of the pain are unknown and understudied, and there is a need for immunocompetent preclinical models of myeloma‐induced bone pain. The aim of this study wa...

Descripción completa

Detalles Bibliográficos
Autores principales: Diaz‐delCastillo, Marta, Kamstrup, Danna, Olsen, Rikke Brix, Hansen, Rie Bager, Pembridge, Thomas, Simanskaite, Brigita, Jimenez‐Andrade, Juan Miguel, Lawson, Michelle A, Heegaard, Anne‐Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017884/
https://www.ncbi.nlm.nih.gov/pubmed/32083236
http://dx.doi.org/10.1002/jbm4.10252
_version_ 1783497268468383744
author Diaz‐delCastillo, Marta
Kamstrup, Danna
Olsen, Rikke Brix
Hansen, Rie Bager
Pembridge, Thomas
Simanskaite, Brigita
Jimenez‐Andrade, Juan Miguel
Lawson, Michelle A
Heegaard, Anne‐Marie
author_facet Diaz‐delCastillo, Marta
Kamstrup, Danna
Olsen, Rikke Brix
Hansen, Rie Bager
Pembridge, Thomas
Simanskaite, Brigita
Jimenez‐Andrade, Juan Miguel
Lawson, Michelle A
Heegaard, Anne‐Marie
author_sort Diaz‐delCastillo, Marta
collection PubMed
description Bone pain is a serious and debilitating symptom of multiple myeloma (MM) that impairs the quality of life of patients. The underlying mechanisms of the pain are unknown and understudied, and there is a need for immunocompetent preclinical models of myeloma‐induced bone pain. The aim of this study was to provide the first in‐depth behavioral characterization of an immunocompetent mouse model of MM presenting the clinical disease features: osteolytic bone disease and bone pain. We hypothesized that a widely used syngeneic model of MM, established by systemic inoculation of green fluorescent protein‐tagged myeloma cells (5TGM1‐GFP) in immunocompetent C57Bl/KaLwRijHsd (BKAL) mice, would present pain‐related behaviors. Disease phenotype was confirmed by splenomegaly, high serum paraprotein, and tumor infiltration in the bone marrow of the hind limbs; however, myeloma‐bearing mice did not present pain‐related behaviors or substantial bone disease. Thus, we investigated an alternative model in which 5TGM1‐GFP cells were directly inoculated into the intrafemoral medullary cavity. This localized myeloma model presented the hallmarks of the disease, including high serum paraprotein, tumor growth, and osteolytic bone lesions. Compared with control mice, myeloma‐bearing mice presented myeloma‐induced pain‐related behaviors, a phenotype that was reversed by systemic morphine treatment. Micro‐computed tomography analyses of the myeloma‐inoculated femurs showed bone disease in cortical and trabecular bone. Repeated systemic bisphosphonate treatment induced an amelioration of the nociceptive phenotype, but did not completely reverse it. Furthermore, intrafemorally injected mice presented a profound denervation of the myeloma‐bearing bones, a previously unknown feature of the disease. This study reports the intrafemoral inoculation of 5TGM1‐GFP cells as a robust immunocompetent model of myeloma‐induced bone pain, with consistent bone loss. Moreover, the data suggest that myeloma‐induced bone pain is caused by a combinatorial mechanism including osteolysis and bone marrow denervation. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research.
format Online
Article
Text
id pubmed-7017884
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-70178842020-02-20 Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma Diaz‐delCastillo, Marta Kamstrup, Danna Olsen, Rikke Brix Hansen, Rie Bager Pembridge, Thomas Simanskaite, Brigita Jimenez‐Andrade, Juan Miguel Lawson, Michelle A Heegaard, Anne‐Marie JBMR Plus Original Articles Bone pain is a serious and debilitating symptom of multiple myeloma (MM) that impairs the quality of life of patients. The underlying mechanisms of the pain are unknown and understudied, and there is a need for immunocompetent preclinical models of myeloma‐induced bone pain. The aim of this study was to provide the first in‐depth behavioral characterization of an immunocompetent mouse model of MM presenting the clinical disease features: osteolytic bone disease and bone pain. We hypothesized that a widely used syngeneic model of MM, established by systemic inoculation of green fluorescent protein‐tagged myeloma cells (5TGM1‐GFP) in immunocompetent C57Bl/KaLwRijHsd (BKAL) mice, would present pain‐related behaviors. Disease phenotype was confirmed by splenomegaly, high serum paraprotein, and tumor infiltration in the bone marrow of the hind limbs; however, myeloma‐bearing mice did not present pain‐related behaviors or substantial bone disease. Thus, we investigated an alternative model in which 5TGM1‐GFP cells were directly inoculated into the intrafemoral medullary cavity. This localized myeloma model presented the hallmarks of the disease, including high serum paraprotein, tumor growth, and osteolytic bone lesions. Compared with control mice, myeloma‐bearing mice presented myeloma‐induced pain‐related behaviors, a phenotype that was reversed by systemic morphine treatment. Micro‐computed tomography analyses of the myeloma‐inoculated femurs showed bone disease in cortical and trabecular bone. Repeated systemic bisphosphonate treatment induced an amelioration of the nociceptive phenotype, but did not completely reverse it. Furthermore, intrafemorally injected mice presented a profound denervation of the myeloma‐bearing bones, a previously unknown feature of the disease. This study reports the intrafemoral inoculation of 5TGM1‐GFP cells as a robust immunocompetent model of myeloma‐induced bone pain, with consistent bone loss. Moreover, the data suggest that myeloma‐induced bone pain is caused by a combinatorial mechanism including osteolysis and bone marrow denervation. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. John Wiley & Sons, Inc. 2019-12-30 /pmc/articles/PMC7017884/ /pubmed/32083236 http://dx.doi.org/10.1002/jbm4.10252 Text en © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. This is an open access article under the terms of the 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
Diaz‐delCastillo, Marta
Kamstrup, Danna
Olsen, Rikke Brix
Hansen, Rie Bager
Pembridge, Thomas
Simanskaite, Brigita
Jimenez‐Andrade, Juan Miguel
Lawson, Michelle A
Heegaard, Anne‐Marie
Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma
title Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma
title_full Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma
title_fullStr Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma
title_full_unstemmed Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma
title_short Differential Pain‐Related Behaviors and Bone Disease in Immunocompetent Mouse Models of Myeloma
title_sort differential pain‐related behaviors and bone disease in immunocompetent mouse models of myeloma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017884/
https://www.ncbi.nlm.nih.gov/pubmed/32083236
http://dx.doi.org/10.1002/jbm4.10252
work_keys_str_mv AT diazdelcastillomarta differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT kamstrupdanna differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT olsenrikkebrix differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT hansenriebager differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT pembridgethomas differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT simanskaitebrigita differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT jimenezandradejuanmiguel differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT lawsonmichellea differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma
AT heegaardannemarie differentialpainrelatedbehaviorsandbonediseaseinimmunocompetentmousemodelsofmyeloma