A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

Bone mechano-response is driven by locomotion transitions during vertebrate evolution




TekijätShimochi, Saeka; Brunet, Clara; Fontcuberta-Rigo, Margalida; Hrovat, Katja; Puigbò, Pere; Nakamura, Miho

KustantajaSpringer Nature

Julkaisuvuosi2025

Lehti: Communications Biology

eISSN2399-3642

DOIhttps://doi.org/10.1038/s42003-025-09292-1

Julkaisun avoimuus kirjaamishetkelläAvoimesti saatavilla

Julkaisukanavan avoimuus Kokonaan avoin julkaisukanava

Verkko-osoitehttps://doi.org/10.1038/s42003-025-09292-1

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/505680246


Tiivistelmä

The skeleton supports the muscles in keeping the body upright against gravity while enduring thousands of daily loads. In this study, we investigated non-collagenous bone matrix proteins using osteoblast cell cultures and phylogenetic analyses to identify the molecular mechanisms involved in mechanical loading. The results indicate that several non-collagenous proteins may significantly regulate the bone’s response to mechanical stress. Furthermore, we hypothesize that the bone mechano-response is an evolutionary-driven process. The selection analysis indicates that two of the major evolutionary transitions in vertebrate locomotion shaped the roles of non-collagenous proteins in the bone matrix: the water-to-land transition, which increased mechanical stress on the limbs, and the evolution to bipedalism in humans, which altered the distribution of stress on the lower and upper limbs. Fetuin A, positively selected in both evolutionary transitions, showed the most significant expression change during the mechanical stimulation experiments.


Ladattava julkaisu

This is an electronic reprint of the original article.
This reprint may differ from the original in pagination and typographic detail. Please cite the original version.




Julkaisussa olevat rahoitustiedot
This study was supported by the Sigrid Juselius Foundation, JSPS Grants-in-Aid for Scientific Research (JP23K08670), the Murata Foundation and the Turku Collegium for Science, Medicine and Technology. This study was supported by the IT-CSC Finland (Project ID #2004931).


Last updated on 2025-02-12 at 10:05