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Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease

Molecular omics technologies, including proteomics, have enabled the elucidation of key signaling pathways that mediate bidirectional communication between the brain and bone tissues. Here we provide a brief summary of the clinical and molecular evidence of the need to study the bone–brain axis of c...

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Autores principales: Schurman, Charles A., Burton, Jordan B., Rose, Jacob, Ellerby, Lisa M., Alliston, Tamara, Schilling, Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Bone and Mineral Research 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036181/
https://www.ncbi.nlm.nih.gov/pubmed/36950837
http://dx.doi.org/10.11005/jbm.2023.30.1.1
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author Schurman, Charles A.
Burton, Jordan B.
Rose, Jacob
Ellerby, Lisa M.
Alliston, Tamara
Schilling, Birgit
author_facet Schurman, Charles A.
Burton, Jordan B.
Rose, Jacob
Ellerby, Lisa M.
Alliston, Tamara
Schilling, Birgit
author_sort Schurman, Charles A.
collection PubMed
description Molecular omics technologies, including proteomics, have enabled the elucidation of key signaling pathways that mediate bidirectional communication between the brain and bone tissues. Here we provide a brief summary of the clinical and molecular evidence of the need to study the bone–brain axis of cross-tissue cellular communication. Clear clinical and molecular evidence suggests biological interactions and similarities between bone and brain cells. Here we review the current mass spectrometric techniques for studying brain and bone diseases with an emphasis on neurodegenerative diseases and osteoarthritis/osteoporosis, respectively. Further study of the bone–brain axis on a molecular level and evaluation of the role of proteins, neuropeptides, osteokines, and hormones in molecular pathways linked to bone and brain diseases is critically needed. The use of mass spectrometry and other omics technologies to analyze these cross-tissue signaling events and interactions will help us better understand disease progression and comorbidities and potentially identify new pathways and targets for therapeutic interventions. Proteomic measurements are particularly favorable for investigating the role of signaling and secreted and circulating analytes and identifying molecular and metabolic pathways implicated in age-related diseases.
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spelling pubmed-100361812023-03-24 Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease Schurman, Charles A. Burton, Jordan B. Rose, Jacob Ellerby, Lisa M. Alliston, Tamara Schilling, Birgit J Bone Metab Review Article Molecular omics technologies, including proteomics, have enabled the elucidation of key signaling pathways that mediate bidirectional communication between the brain and bone tissues. Here we provide a brief summary of the clinical and molecular evidence of the need to study the bone–brain axis of cross-tissue cellular communication. Clear clinical and molecular evidence suggests biological interactions and similarities between bone and brain cells. Here we review the current mass spectrometric techniques for studying brain and bone diseases with an emphasis on neurodegenerative diseases and osteoarthritis/osteoporosis, respectively. Further study of the bone–brain axis on a molecular level and evaluation of the role of proteins, neuropeptides, osteokines, and hormones in molecular pathways linked to bone and brain diseases is critically needed. The use of mass spectrometry and other omics technologies to analyze these cross-tissue signaling events and interactions will help us better understand disease progression and comorbidities and potentially identify new pathways and targets for therapeutic interventions. Proteomic measurements are particularly favorable for investigating the role of signaling and secreted and circulating analytes and identifying molecular and metabolic pathways implicated in age-related diseases. The Korean Society for Bone and Mineral Research 2023-02 2023-02-28 /pmc/articles/PMC10036181/ /pubmed/36950837 http://dx.doi.org/10.11005/jbm.2023.30.1.1 Text en Copyright © 2023 The Korean Society for Bone and Mineral Research https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Schurman, Charles A.
Burton, Jordan B.
Rose, Jacob
Ellerby, Lisa M.
Alliston, Tamara
Schilling, Birgit
Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease
title Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease
title_full Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease
title_fullStr Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease
title_full_unstemmed Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease
title_short Molecular and Cellular Crosstalk between Bone and Brain: Accessing Bidirectional Neural and Musculoskeletal Signaling during Aging and Disease
title_sort molecular and cellular crosstalk between bone and brain: accessing bidirectional neural and musculoskeletal signaling during aging and disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036181/
https://www.ncbi.nlm.nih.gov/pubmed/36950837
http://dx.doi.org/10.11005/jbm.2023.30.1.1
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