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dc.contributor.authorRoschger, A
dc.contributor.authorRoschger, P
dc.contributor.authorWagermaier, W
dc.contributor.authorChen, J
dc.contributor.authorvan Tol, A
dc.contributor.authorRepp, F
dc.contributor.authorBlouin, S
dc.contributor.authorBerzlanovich, AM
dc.contributor.authorGruber, GM
dc.contributor.authorKlaushofer, K
dc.contributor.authorFratzl, P
dc.contributor.authorWeinkamer, R
dc.date.accessioned2019-04-29T07:52:49Z
dc.date.issued2019-03-18
dc.description.abstractThe osteocyte lacunar-canalicular network (LCN) penetrates bone and houses the osteocytes and their processes. Despite its rather low volume fraction, the LCN represents an outstanding large surface that is possibly used by the osteocytes to interact with the surrounding mineralized bone matrix thereby contributing to mineral homeostasis. The aim of this study was to quantitatively describe such contributions by spatially correlating the local density of the LCN with the mineral content at the same location in micrometer-sized volume elements in human osteons. For this purpose, 65 osteons from the femur midshaft from healthy adults (n = 4) and children (n = 2) were structurally characterized with two different techniques. The 3D structure of the LCN in the osteons was imaged with confocal laser scanning microscopy after staining the bone samples with rhodamine. Subsequent image analysis provided the canalicular length density, i.e. the total length of the canaliculi per unit volume (μm/μm3). Quantitative information on the mineral content (wt%Ca) from the identical regions was obtained using quantitative backscattered electron imaging. As the LCN-porosity lowers the mineral content, a negative correlation between Ca content and network density was expected. Calculations predict a reduction of around −0.97 fmol Ca per μm of network. However, the experiment revealed for 62 out of 65 osteons a positive correlation resulting in an average additional Ca loading of +1.15 fmol per μm of canalicular network, i.e. an accumulation of mineral has occurred at dense network regions. We hypothesize that this accumulation happens in the close vicinity of canaliculi forming mineral reservoirs that can be utilized by osteocytes. Significant differences found between individuals indicate that the extent of mineral loading of the reservoir zone reflects an important parameter for mineral homeostasis.en_GB
dc.description.sponsorshipGerman Federal Ministry of Education and Researchen_GB
dc.description.sponsorshipAUVA (Research Funds of the Austrian Workers Compensation Board, Austria)en_GB
dc.description.sponsorshipWGKK (Viennese sickness insurance funds, Austria).en_GB
dc.identifier.citationVol. 123, pp. 76 - 85en_GB
dc.identifier.doi10.1016/j.bone.2019.03.018
dc.identifier.grantnumber01EC1402Den_GB
dc.identifier.urihttp://hdl.handle.net/10871/36920
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rights.embargoreasonUnder embargo until 18 March 2020 in compliance with publisher policy.en_GB
dc.rights© 2019 Elsevier Inc. All rights reserved. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  en_GB
dc.subjectOsteocytic osteolysisen_GB
dc.subjectOsteocyte networken_GB
dc.subjectCanaliculien_GB
dc.subjectMineralizationen_GB
dc.subjectOsteonsen_GB
dc.subjectOsteocyteen_GB
dc.titleThe contribution of the pericanalicular matrix to mineral content in human osteonal boneen_GB
dc.typeArticleen_GB
dc.date.available2019-04-29T07:52:49Z
dc.identifier.issn8756-3282
dc.descriptionThis is the author accepted manuscript. The final version is available from Elsevier via the DOI in this record.en_GB
dc.identifier.journalBONEen_GB
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dcterms.dateAccepted2019-03-15
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2019-03-18
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-04-27T11:09:03Z
refterms.versionFCDAM
refterms.panelBen_GB


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© 2019 Elsevier Inc. All rights reserved. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/  
Except where otherwise noted, this item's licence is described as © 2019 Elsevier Inc. All rights reserved. This version is made available under the CC-BY-NC-ND 4.0 license: https://creativecommons.org/licenses/by-nc-nd/4.0/