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Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis
Age‐related (type‐II) osteoporosis is a common and debilitating condition driven in part by the loss of bone marrow (BM) mesenchymal stromal cells (MSC) and their osteoblast progeny, leading to reduced bone formation. Current pharmacological regiments targeting age‐related osteoporosis do not direct...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430063/ https://www.ncbi.nlm.nih.gov/pubmed/28834263 http://dx.doi.org/10.1002/sctm.17-0054 |
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author | Kiernan, Jeffrey Davies, John E. Stanford, William L. |
author_facet | Kiernan, Jeffrey Davies, John E. Stanford, William L. |
author_sort | Kiernan, Jeffrey |
collection | PubMed |
description | Age‐related (type‐II) osteoporosis is a common and debilitating condition driven in part by the loss of bone marrow (BM) mesenchymal stromal cells (MSC) and their osteoblast progeny, leading to reduced bone formation. Current pharmacological regiments targeting age‐related osteoporosis do not directly treat the disease by increasing bone formation, but instead use bisphosphonates to reduce bone resorption—a treatment designed for postmenopausal (type‐I) osteoporosis. Recently, the bone regenerative capacity of MSCs has been found within a very rare population of skeletal stem cells (SSCs) residing within the larger heterogeneous BM‐MSC pool. The osteoregenerative potential of SSCs would be an ideal candidate for cell‐based therapies to treat degenerative bone diseases such as osteoporosis. However, to date, clinical and translational studies attempting to improve bone formation through cell transplantation have used the larger, nonspecific, MSC pool. In this review, we will outline the physiological basis of age‐related osteoporosis, as well as discuss relevant preclinical studies that use exogenous MSC transplantation with the aim of treating osteoporosis in murine models. We will also discuss results from specific clinical trials aimed at treating other systemic bone diseases, and how the discovery of SSC could help realize the full regenerative potential of MSC therapy to increase bone formation. Finally, we will outline how ancillary clinical trials could be initiated to assess MSC/SSC‐mediated bone formation gains in existing and potentially unrelated clinical trials, setting the stage for a dedicated clinical investigation to treat age‐related osteoporosis. Stem Cells Translational Medicine 2017;6:1930–1939 |
format | Online Article Text |
id | pubmed-6430063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64300632019-04-01 Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis Kiernan, Jeffrey Davies, John E. Stanford, William L. Stem Cells Transl Med Translational Research Articles and Reviews Age‐related (type‐II) osteoporosis is a common and debilitating condition driven in part by the loss of bone marrow (BM) mesenchymal stromal cells (MSC) and their osteoblast progeny, leading to reduced bone formation. Current pharmacological regiments targeting age‐related osteoporosis do not directly treat the disease by increasing bone formation, but instead use bisphosphonates to reduce bone resorption—a treatment designed for postmenopausal (type‐I) osteoporosis. Recently, the bone regenerative capacity of MSCs has been found within a very rare population of skeletal stem cells (SSCs) residing within the larger heterogeneous BM‐MSC pool. The osteoregenerative potential of SSCs would be an ideal candidate for cell‐based therapies to treat degenerative bone diseases such as osteoporosis. However, to date, clinical and translational studies attempting to improve bone formation through cell transplantation have used the larger, nonspecific, MSC pool. In this review, we will outline the physiological basis of age‐related osteoporosis, as well as discuss relevant preclinical studies that use exogenous MSC transplantation with the aim of treating osteoporosis in murine models. We will also discuss results from specific clinical trials aimed at treating other systemic bone diseases, and how the discovery of SSC could help realize the full regenerative potential of MSC therapy to increase bone formation. Finally, we will outline how ancillary clinical trials could be initiated to assess MSC/SSC‐mediated bone formation gains in existing and potentially unrelated clinical trials, setting the stage for a dedicated clinical investigation to treat age‐related osteoporosis. Stem Cells Translational Medicine 2017;6:1930–1939 John Wiley and Sons Inc. 2017-08-18 /pmc/articles/PMC6430063/ /pubmed/28834263 http://dx.doi.org/10.1002/sctm.17-0054 Text en © 2017 The Authors stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Translational Research Articles and Reviews Kiernan, Jeffrey Davies, John E. Stanford, William L. Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis |
title | Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis |
title_full | Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis |
title_fullStr | Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis |
title_full_unstemmed | Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis |
title_short | Concise Review: Musculoskeletal Stem Cells to Treat Age‐Related Osteoporosis |
title_sort | concise review: musculoskeletal stem cells to treat age‐related osteoporosis |
topic | Translational Research Articles and Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430063/ https://www.ncbi.nlm.nih.gov/pubmed/28834263 http://dx.doi.org/10.1002/sctm.17-0054 |
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