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  Spatial variations in the osteocyte lacuno-canalicular network density and analysis of the connectomic parameters

Chen, J., Aido, M., Roschger, A., Van Tol, A., Checa, S., Willie, B. M., et al. (2024). Spatial variations in the osteocyte lacuno-canalicular network density and analysis of the connectomic parameters. PLoS ONE, 19(5): e0303515. doi:10.1371/journal.pone.0303515.

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Chen, Junning1, Autor           
Aido, Marta, Autor
Roschger, Andreas2, Autor           
Van Tol, Alexander1, Autor           
Checa, Sara, Autor
Willie, Bettina M., Autor
Weinkamer, Richard1, Autor           
Affiliations:
1Richard Weinkamer, Biomaterialien, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863295              
2Wolfgang Wagermaier, Biomaterialien, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863296              

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 Zusammenfassung: Osteocyte lacuno-canalicular network (LCN) is comprised of micrometre-sized pores and submicrometric wide channels in bone. Accumulating evidence suggests multiple functions of this network in material transportation, mechanobiological signalling, mineral homeostasis and bone remodelling. Combining rhodamine staining and confocal laser scanning microscopy, the longitudinal cross-sections of six mouse tibiae were imaged, and the connectome of the network was quantified with a focus on the spatial heterogeneities of network density, connectivity and length of canaliculi. In-vivo loading and double calcein labelling on these tibiae allowed differentiating the newly formed bone from the pre-existing regions. The canalicular density of the murine cortical bone varied between 0.174 and 0.243 μm/μmy3, and therefore is three times larger than the corresponding value for human femoral midshaft osteons. The spatial heterogeneity of the network was found distinctly more pronounced across the cortex than along the cortex. We found that in regions with a dense network, the LCN conserves its largely tree-like character, but increases the density by including shorter canaliculi. The current study on healthy mice should serve as a motivating starting point to study the connectome of genetically modified mice, including models of bone diseases and of reduced mechanoresponse.

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Sprache(n): eng - English
 Datum: 2024-05-142024
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1371/journal.pone.0303515
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Titel: PLoS ONE
  Kurztitel : PLOS ONE
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: San Francisco, CA : Public Library of Science
Seiten: - Band / Heft: 19 (5) Artikelnummer: e0303515 Start- / Endseite: - Identifikator: ISSN: 1932-6203