Literature DB >> 23352996

Osteocytes remove and replace perilacunar mineral during reproductive cycles.

John J Wysolmerski1.   

Abstract

Lactation is associated with an increased demand for calcium and is accompanied by a remarkable cycle of bone loss and recovery that helps to supply calcium and phosphorus for milk production. Bone loss is the result of increased bone resorption that is due, in part, to increased levels of PTHrP and decreased levels of estrogen. However, the regulation of bone turnover during this time is not fully understood. In the 1960s and 1970s many observations were made to suggest that osteocytes could resorb bone and increase the size of their lacunae. This concept became known as osteocytic osteolysis and studies suggested that it occurred in response to parathyroid hormone and/or an increased systemic demand for calcium. However, this concept fell out of favor in the late 1970s when it was established that osteoclasts were the principal bone-resorbing cells. Given that lactation is associated with increased PTHrP levels and negative calcium balance, we recently examined whether osteocytes contribute to bone loss during this time. Our findings suggest that osteocytes can remodel their perilacunar and pericanalicular matrix and that they participate in the liberation of skeletal calcium stores during reproductive cycles. These findings raise new questions about the role of osteocytes in coordinating bone and mineral metabolism during lactation as well as the recovery of bone mass after weaning. It is also interesting to consider whether osteocyte lacunar and canalicular remodeling contribute more broadly to the maintenance of skeletal and mineral homeostasis.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23352996      PMCID: PMC3624069          DOI: 10.1016/j.bone.2013.01.025

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  61 in total

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  36 in total

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Authors:  Brittany A Ryan; Christopher S Kovacs
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2.  Osteocyte-Intrinsic TGF-β Signaling Regulates Bone Quality through Perilacunar/Canalicular Remodeling.

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Review 4.  Molecular and cellular basis of bone resorption.

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Journal:  Wien Med Wochenschr       Date:  2014-09-16

5.  Cathepsin K-deficient osteocytes prevent lactation-induced bone loss and parathyroid hormone suppression.

Authors:  Sutada Lotinun; Yoshihito Ishihara; Kenichi Nagano; Riku Kiviranta; Vincent T Carpentier; Lynn Neff; Virginia Parkman; Noriko Ide; Dorothy Hu; Pamela Dann; Daniel Brooks; Mary L Bouxsein; John Wysolmerski; Francesca Gori; Roland Baron
Journal:  J Clin Invest       Date:  2019-05-21       Impact factor: 14.808

6.  Parallel mechanisms suppress cochlear bone remodeling to protect hearing.

Authors:  Emmanuel J Jáuregui; Omar Akil; Claire Acevedo; Faith Hall-Glenn; Betty S Tsai; Hrishikesh A Bale; Ellen Liebenberg; Mary Beth Humphrey; Robert O Ritchie; Lawrence R Lustig; Tamara Alliston
Journal:  Bone       Date:  2016-04-13       Impact factor: 4.398

Review 7.  Emerging insights into the comparative effectiveness of anabolic therapies for osteoporosis.

Authors:  Eben G Estell; Clifford J Rosen
Journal:  Nat Rev Endocrinol       Date:  2020-11-04       Impact factor: 43.330

Review 8.  The Osteocyte: New Insights.

Authors:  Alexander G Robling; Lynda F Bonewald
Journal:  Annu Rev Physiol       Date:  2020-02-10       Impact factor: 19.318

9.  Osteocytic Osteolysis in PTH-treated Wild-type and Rankl-/- Mice Examined by Transmission Electron Microscopy, Atomic Force Microscopy, and Isotope Microscopy.

Authors:  Hiromi Hongo; Tomoka Hasegawa; Masami Saito; Kanako Tsuboi; Tomomaya Yamamoto; Muneteru Sasaki; Miki Abe; Paulo Henrique Luiz de Freitas; Hisayoshi Yurimoto; Nobuyuki Udagawa; Minqi Li; Norio Amizuka
Journal:  J Histochem Cytochem       Date:  2020-09-18       Impact factor: 2.479

10.  Calcium fluxes at the bone/plasma interface: Acute effects of parathyroid hormone (PTH) and targeted deletion of PTH/PTH-related peptide (PTHrP) receptor in the osteocytes.

Authors:  Christopher Dedic; Tin Shing Hung; Alan M Shipley; Akira Maeda; Thomas Gardella; Andrew L Miller; Paola Divieti Pajevic; Joseph G Kunkel; Alessandro Rubinacci
Journal:  Bone       Date:  2018-07-24       Impact factor: 4.398

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