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β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6
The requirement for LRP5 and LRP6 to prevent β-catenin degradation in the absence of the tumor suppressor APC is unclear because cell culture models have yielded conflicting results. We previously established that osteoblast-specific loss of APC causes β-catenin accumulation and increased bone mass,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613880/ https://www.ncbi.nlm.nih.gov/pubmed/37908496 http://dx.doi.org/10.17912/micropub.biology.001000 |
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author | Diegel, Cassandra R. Michalski, Megan N. Williams, Bart O. |
author_facet | Diegel, Cassandra R. Michalski, Megan N. Williams, Bart O. |
author_sort | Diegel, Cassandra R. |
collection | PubMed |
description | The requirement for LRP5 and LRP6 to prevent β-catenin degradation in the absence of the tumor suppressor APC is unclear because cell culture models have yielded conflicting results. We previously established that osteoblast-specific loss of APC causes β-catenin accumulation and increased bone mass, while loss of both LRP5 and LRP6 reduces bone mass. We report here that the simultaneous loss of APC, LRP5, and LRP6 in osteoblasts in mice phenocopies the APC osteoblast-specific knockout. Thus, β-catenin stabilization and increased bone mass after loss of APC in osteoblasts in vivo are not dependent on LRP5 and LRP6. |
format | Online Article Text |
id | pubmed-10613880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Caltech Library |
record_format | MEDLINE/PubMed |
spelling | pubmed-106138802023-10-31 β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6 Diegel, Cassandra R. Michalski, Megan N. Williams, Bart O. MicroPubl Biol Findings Previously Not Shown The requirement for LRP5 and LRP6 to prevent β-catenin degradation in the absence of the tumor suppressor APC is unclear because cell culture models have yielded conflicting results. We previously established that osteoblast-specific loss of APC causes β-catenin accumulation and increased bone mass, while loss of both LRP5 and LRP6 reduces bone mass. We report here that the simultaneous loss of APC, LRP5, and LRP6 in osteoblasts in mice phenocopies the APC osteoblast-specific knockout. Thus, β-catenin stabilization and increased bone mass after loss of APC in osteoblasts in vivo are not dependent on LRP5 and LRP6. Caltech Library 2023-10-15 /pmc/articles/PMC10613880/ /pubmed/37908496 http://dx.doi.org/10.17912/micropub.biology.001000 Text en Copyright: © 2023 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Findings Previously Not Shown Diegel, Cassandra R. Michalski, Megan N. Williams, Bart O. β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6 |
title | β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6 |
title_full | β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6 |
title_fullStr | β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6 |
title_full_unstemmed | β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6 |
title_short | β-catenin-dependent High Bone Mass Induced by Loss of APC in Osteoblasts Does Not Require Lrp5 or Lrp6 |
title_sort | β-catenin-dependent high bone mass induced by loss of apc in osteoblasts does not require lrp5 or lrp6 |
topic | Findings Previously Not Shown |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613880/ https://www.ncbi.nlm.nih.gov/pubmed/37908496 http://dx.doi.org/10.17912/micropub.biology.001000 |
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