Evidence map›Paper›PMID 38743675›Full record

ArticlePloS one2024

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

Junning Chen, Marta Aido, Andreas Roschger, Alexander van Tol, Sara Checa, Bettina M Willie, Richard Weinkamer

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Bone matrix proteins: regulators of skeletal remodeling and repair.Journal of bone and mineral metabolism · 2026
    Review
  4. Rethinking osteocyte modelsFrontiers in bioengineering and biotechnology · 2026
    Review
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Junning ChenDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.ORCID 0000-0001-7121-0994
Marta AidoJulius Wolff Institute, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Andreas RoschgerDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.
Alexander van TolDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.
Sara ChecaJulius Wolff Institute, Charité-Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0002-1444-5858
Bettina M WillieDepartment of Pediatric Surgery, Research Centre, Shriners Hospital for Children-Canada, McGill University, Montreal, Canada.ORCID 0000-0003-2907-3580
Richard WeinkamerDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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/μm3, 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.

Indexed as

ConnectomeOsteocytesAnimalsHumansMiceMice, Inbred C57BLMicroscopy, ConfocalTibia

Identifiers

PMID38743675
PMCPMC11093372

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.