Evidence map›Paper›PMID 41624533›Full record

ArticleMaterials today. Bio2026

Nano-scale evidence for osteocyte network integration across bone remodeling interfaces in human bone revealed by synchrotron nanoCT.

Sophie Anuth, Emely Bortel, Julie Villanova, Jussi-Petteri Suuronen, Sven Geissler, Amaia Cipitria, Peter Fratzl, Tobias Fretwurst, Katja Nelson, Susanne Nahles and 1 more

Abstract read
In one paragraph

Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Sophie AnuthXploraytion GmbH, Invalidenstrasse 34, 10115, Berlin, Germany.
Emely BortelXploraytion GmbH, Invalidenstrasse 34, 10115, Berlin, Germany.
Julie VillanovaESRF - European Synchrotron Facility, Avenue des Martyrs 71, 38043, Grenoble, France.
Jussi-Petteri SuuronenXploraytion GmbH, Invalidenstrasse 34, 10115, Berlin, Germany.
Sven GeisslerBerlin Institute of Health Center for Regenerative Therapies, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Amaia CipitriaGroup of Bioengineering in Regeneration and Cancer, Biogipuzkoa Health Research Institute, San Sebastián, Spain.
Peter FratzlDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, Max Planck Society, Am Mühlenberg 1 OT Golm, 14476, Potsdam, Germany.
Tobias FretwurstDepartment of Oral and Craniomaxillofacial Surgery/Translational Implantology, Center for Dental Medicine, Medical Center, Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg, 79106, Germany.
Katja NelsonDepartment of Oral and Craniomaxillofacial Surgery/Translational Implantology, Center for Dental Medicine, Medical Center, Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg, 79106, Germany.
Susanne NahlesDepartment of Craniomaxillofacial Surgery, Charité, CVK, Augustenburger Platz 1, Berlin, 13353, Germany.
Bernhard HesseXploraytion GmbH, Invalidenstrasse 34, 10115, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone remodeling is a highly regulated, hierarchical process critical for maintaining structural integrity and mineral homeostasis. At the nano-scale, the osteocytes orchestrate mechanosensing, signaling, and nutrient transport across the mineralized matrix utilizing their extensive network of cell dendrites. The lacunar-canalicular network (OLCN) houses the cellular components within the matrix. How this network integrates across bone regions formed during different remodeling cycles remains unresolved. How the cellular network is connected across interfaces between different remodeling regions or cement lines is the focus of this exploration: is the network integration merely stochastical occurrences or result of a cued, directed formation process? Using synchrotron-based nano computed tomography (nano-CT), we analyze human bone samples of 35 different patients with sub-micron resolution to characterize canalicular structures around cement lines. The results show the network's ability and affinity to integrate, and the strong influence of local tissue conditions on the degree of integration. We novelly include the structural analysis of canalicular network architecture to interpret underlying formation processes. Besides 'cross-generational' canalicular connections, we identify previously overlooked canalicular loops in newly formed bone near cement lines and interpret these as morphological indicators of a directed, adaptive search for reconnection. The study suggests a mechanism combining random outgrowth and directed progression influenced by local cues. We propose a 'cross-generational' OLCN: a deliberately integrated network that enhances tissue connectivity, functional resilience, and osteocyte survival across temporal remodeling stages. These findings advance the understanding of bone network complexity and introduce canalicular looping as a nano-structural signature of directed formation in bone network architecture.

Indexed as

Bone remodelingBone tissue nano-architectureCanalicular connectivityCement linesOsteocyte lacunar-canalicular network (OLCN)Synchrotron nano computed tomography

Identifiers

PMID41624533
PMCPMC12859465

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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.