» Articles » PMID: 22308018

Demonstration of Osteocytic Perilacunar/canalicular Remodeling in Mice During Lactation

Overview
Date 2012 Feb 7
PMID 22308018
Citations 237
Authors
Affiliations
Soon will be listed here.
Abstract

Osteoclasts are thought to be solely responsible for the removal of bone matrix. However, we show here that osteocytes can also remove bone matrix by reversibly remodeling their perilacunar/canalicular matrix during the reproductive cycle. In contrast, no osteocytic remodeling was observed with experimental unloading despite similar degrees of bone loss. Gene array analysis of osteocytes from lactating animals revealed an elevation of genes known to be utilized by osteoclasts to remove bone, including tartrate-resistant acid phosphatase (TRAP) and cathepsin K, that returned to virgin levels upon weaning. Infusion of parathyroid hormone-related peptide (PTHrP), known to be elevated during lactation, induced TRAP activity and cathepsin K expression in osteocytes concurrent with osteocytic remodeling. Conversely, animals lacking the parathyroid hormone type 1 receptor (PTHR1) in osteocytes failed to express TRAP or cathepsin K or to remodel their osteocyte perilacunar matrix during lactation. These studies show that osteocytes remove mineralized matrix through molecular mechanisms similar to those utilized by osteoclasts.

Citing Articles

Articular cartilage degeneration and aberrant osteocyte perilacunar/canalicular remodeling in subchondral bone of patients with developmental dysplasia of the hip.

Ye T, Yan J, Kan T, Xie G, Zhang Z, Yin W BMC Musculoskelet Disord. 2025; 26(1):165.

PMID: 39966795 PMC: 11837434. DOI: 10.1186/s12891-025-08419-z.


Understanding the structural biology of osteomalacia through multiscale 3D X-ray and electron tomographic imaging: a review of X-linked hypophosphatemia, the mouse model, and imaging methods.

Buss D, Deering J, Reznikov N, McKee M JBMR Plus. 2025; 9(2):ziae176.

PMID: 39896117 PMC: 11783288. DOI: 10.1093/jbmrpl/ziae176.


Conditional Deletion of Gremlin-1 in Cathepsin K-expressing Mature Osteoclasts Altered the Skeletal Response to Calcium Depletion in Sex-Dependent Manner.

Sheng M, Rundle C, Baylink D, Lau K Calcif Tissue Int. 2025; 116(1):28.

PMID: 39789342 PMC: 11717885. DOI: 10.1007/s00223-024-01337-7.


CCN3: lactational bone booster.

Xu N, Yang K, Wang M Cell Biosci. 2024; 14(1):155.

PMID: 39734229 PMC: 11684062. DOI: 10.1186/s13578-024-01344-z.


Current and future perspectives on pregnancy and lactation-associated osteoporosis.

Gak N, Abbara A, Dhillo W, Keen R, Comninos A Front Endocrinol (Lausanne). 2024; 15:1494965.

PMID: 39703866 PMC: 11655223. DOI: 10.3389/fendo.2024.1494965.


References
1.
BELANGER L, Drouin P . Osteolysis in the frog. The effects of parathormone. Can J Physiol Pharmacol. 1966; 44(6):919-22. DOI: 10.1139/y66-114. View

2.
Fermor B, Skerry T . PTH/PTHrP receptor expression on osteoblasts and osteocytes but not resorbing bone surfaces in growing rats. J Bone Miner Res. 1995; 10(12):1935-43. DOI: 10.1002/jbmr.5650101213. View

3.
Nakano Y, Toyosawa S, Takano Y . Eccentric localization of osteocytes expressing enzymatic activities, protein, and mRNA signals for type 5 tartrate-resistant acid phosphatase (TRAP). J Histochem Cytochem. 2004; 52(11):1475-82. PMC: 3957824. DOI: 10.1369/jhc.4A6378.2004. View

4.
Tazawa K, Hoshi K, Kawamoto S, Tanaka M, Ejiri S, Ozawa H . Osteocytic osteolysis observed in rats to which parathyroid hormone was continuously administered. J Bone Miner Metab. 2004; 22(6):524-9. DOI: 10.1007/s00774-004-0519-x. View

5.
Gu G, Nars M, Hentunen T, Metsikko K, Vaananen H . Isolated primary osteocytes express functional gap junctions in vitro. Cell Tissue Res. 2005; 323(2):263-71. DOI: 10.1007/s00441-005-0066-3. View