Evidence map›Paper›PMID 42881197›Full record

ArticleNature communications2026

Tissue composition shapes differential skeletal integration strategies during axolotl limb regeneration.

Rita Aires, Sean D Keeley, Kerstin Brandt, Mário Carreira, Doğa Berşan Güneş, Yağız Savcı, Pedro Capucho, Ulrike Anne Friedrich, Andreas Dahl, Can Aztekin and 1 more

Abstract read
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In one paragraph

Article in Nature communications, 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.

Rita AiresDepartment of Internal Medicine III, Center for Healthy Aging, University Hospital and Faculty of Medicine Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany. rita.aires@tu-dresden.de.ORCID http://orcid.org/0000-0002-3537-0453
Sean D KeeleyDepartment of Internal Medicine III, Center for Healthy Aging, University Hospital and Faculty of Medicine Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany.ORCID http://orcid.org/0000-0002-2429-3253
Kerstin BrandtCenter for Regenerative Therapies Dresden (CRTD), Center for Molecular and Cellular Bioengineering (CMCB), TUD Dresden University of Technology, Dresden, Germany.
Mário CarreiraDepartment of Internal Medicine III, Center for Healthy Aging, University Hospital and Faculty of Medicine Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany.ORCID http://orcid.org/0009-0005-4772-4449
Doğa Berşan GüneşGraduate School of Science and Engineering, Yıldız Technical University, Esenler/Istanbul, Türkiye.ORCID http://orcid.org/0009-0005-1949-8165
Yağız SavcıCenter for Regenerative Therapies Dresden (CRTD), Center for Molecular and Cellular Bioengineering (CMCB), TUD Dresden University of Technology, Dresden, Germany.ORCID http://orcid.org/0000-0003-1198-9099
Pedro CapuchoNOVA Medical School, Faculdade de Ciências Médicas, NMS, FCM, NOVA University Lisbon, Lisboa, Portugal.ORCID http://orcid.org/0009-0006-7416-4923
Ulrike Anne FriedrichPaul Langerhans Institute Dresden of the Helmholtz Center Munich, University Hospital and Faculty of Medicine Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany.
Andreas DahlDRESDEN-concept Genome Center (DcGC), Center for Molecular and Cellular Bioengineering (CMCB) Technology Platform, TUD Dresden University of Technology, Dresden, Germany.
Can AztekinFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Tatiana Sandoval-GuzmánDepartment of Internal Medicine III, Center for Healthy Aging, University Hospital and Faculty of Medicine Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany. tatiana.sandoval_guzman@tu-dresden.de.ORCID http://orcid.org/0000-0003-1802-5145

Funding

Alexander von Humboldt-Stiftung (Alexander von Humboldt Foundation) PRT 1208176 HFST-PDeutsche Forschungsgemeinschaft (German Research Foundation) AI 214/1-1
6 · The paper itself

Abstract

Limb regeneration requires rebuilding the missing structures and integrating them with stump tissues. Osteoclast-mediated tissue resorption is essential for skeletal integration during regeneration. However, it is unknown if skeletal tissue composition impacts its resorption and, if so, how it is regulated. Here, we show that osteoclast-mediated skeletal resorption is activated in amputations damaging the diaphysis, but not the epiphysis, of skeletal elements. We found that amputations in the calcified diaphysis trigger the sustained expression of RANKL and the chemokine Loc483, and that the latter is sufficient to induce osteoclast presence in non-resorbing amputations. Finally, our data suggests that the transcriptomic profile of the apical epithelial cap is impacted by the tissues injured by the amputation. Overall, our work reveals that tissue composition at the amputation plane shapes adaptations of the regenerative program, which ultimately contribute to the near-seamless tissue integration of the regenerating axolotl limb regardless of the amputation position.

Indexed as

Ambystoma mexicanumExtremitiesRegenerationAmputation, SurgicalAnimalsOsteoclastsRANK LigandTranscriptomeRANK Ligand

Identifiers

PMID42881197

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.