Literature DB >> 33963821

3D Interrelationship between Osteocyte Network and Forming Mineral during Human Bone Remodeling.

Mahdi Ayoubi1,2, Alexander F van Tol1,2, Richard Weinkamer1, Paul Roschger3, Peter C Brugger4, Andrea Berzlanovich5, Luca Bertinetti1,6, Andreas Roschger1,7, Peter Fratzl1.   

Abstract

During bone remodeling, osteoblasts are known to deposit unmineralized collagenous tissue (osteoid), which mineralizes after some time lag. Some of the osteoblasts differentiate into osteocytes, forming a cell network within the lacunocanalicular network (LCN) of bone. To get more insight into the potential role of osteocytes in the mineralization process of osteoid, sites of bone formation are three-dimensionally imaged in nine forming human osteons using focused ion beam-scanning electron microscopy (FIB-SEM). In agreement with previous observations, the mineral concentration is found to gradually increase from the central Haversian canal toward pre-existing mineralized bone. Most interestingly, a similar feature is discovered on a length scale more than 100-times smaller, whereby mineral concentration increases from the LCN, leaving around the canaliculi a zone virtually free of mineral, the size of which decreases with progressing mineralization. This suggests that the LCN controls mineral formation but not just by diffusion of mineralization precursors, which would lead to a continuous decrease of mineral concentration from the LCN. The observation is, however, compatible with the codiffusion and reaction of precursors and inhibitors from the LCN into the bone matrix.
© 2021 The Authors. Advanced Healthcare Materials published by Wiley-VCH GmbH.

Entities:  

Keywords:  FIB-SEM tomography; biomineralization; bone remodeling; iodine vapor staining; lacunocanalicular network (LCN); mineralization foci

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Year:  2021        PMID: 33963821     DOI: 10.1002/adhm.202100113

Source DB:  PubMed          Journal:  Adv Healthc Mater        ISSN: 2192-2640            Impact factor:   9.933


  3 in total

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2.  Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials.

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  3 in total

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