The regenerative effect of exosomes isolated from mouse embryonic fibroblasts in mice created as a sciatic nerve crush injury model
Publication type: Journal Article
Publication date: 2024-10-10
scimago Q2
wos Q3
SJR: 0.710
CiteScore: 5.0
Impact factor: 2.8
ISSN: 03014851, 15734978
PubMed ID:
39388029
Abstract
Exosomes (Exos) are candidates for functional recovery and regeneration following sciatic nerve crushed (SNC) injury due to their composition which can accelerate tissue regeneration. Therefore, mouse embryonic fibroblast-derived exosomes were evaluated for their regenerative capacity in SNC injury. In the study, 40 Balb/c males (20 ± 5 g) and two pregnant mice (for embryonic fibroblast tissue) were used and crushed injury was induced in the left sciatic nerve with an aneurysm clamp. Sciatic nerve model mice were randomly divided into 5 groups (n = 8; control, n = 8; sham, n = 8; SNC, n = 8; Mouse embryonic fibroblast exosome (mExo), n = 8; SNC + Mouse embryonic fibroblast exosome (SNC + mExo). Rotarod tests for motor functions and hot plate and von Frey tests for sensory functions were analyzed in the groups. Expression changes of exosome genes (RARRES1, NAGS, HOXA13, and MEIS1) immunohistochemical analysis of these gene proteins, and structural exosome NF-200 and S100 proteins were evaluated by confocal microscopy. Behavioral analyses showed that the damage in SNC was significant between groups on day14 and day28 (P < 0.05). In behavioral analyses, it was determined that motor functions and mechanical sensitivity lost in SNC were regained after mExo treatment. While expression of all genes was detected in MEF-derived exosomes, the high expression was MESI1 and the low expression was HOXA13. NF200, an indicator of axon number and neurofilament density, was found to decrease in SNC (P < 0.001) and increase after treatment, but not significantly. The decreased S100 protein levels in SNC and the increase detected after treatment were not significant. The expression of four mRNAs in mExos indicates that these genes may have an effect on regenerative processes after SNC injury. The regenerative process supported by tissue protein expressions demonstrates the therapeutic potential of mExo treatment.
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BOZKURT A. S. et al. The regenerative effect of exosomes isolated from mouse embryonic fibroblasts in mice created as a sciatic nerve crush injury model // Molecular Biology Reports. 2024. Vol. 51. No. 1. 1046
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BOZKURT A. S., Görücü Yilmaz Ş., Kaplan D. S., Bal R. The regenerative effect of exosomes isolated from mouse embryonic fibroblasts in mice created as a sciatic nerve crush injury model // Molecular Biology Reports. 2024. Vol. 51. No. 1. 1046
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TY - JOUR
DO - 10.1007/s11033-024-09962-z
UR - https://link.springer.com/10.1007/s11033-024-09962-z
TI - The regenerative effect of exosomes isolated from mouse embryonic fibroblasts in mice created as a sciatic nerve crush injury model
T2 - Molecular Biology Reports
AU - BOZKURT, AHMET S.
AU - Görücü Yilmaz, Şenay
AU - Kaplan, Davut Sinan
AU - Bal, Ramazan
PY - 2024
DA - 2024/10/10
PB - Springer Nature
IS - 1
VL - 51
PMID - 39388029
SN - 0301-4851
SN - 1573-4978
ER -
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@article{2024_BOZKURT,
author = {AHMET S. BOZKURT and Şenay Görücü Yilmaz and Davut Sinan Kaplan and Ramazan Bal},
title = {The regenerative effect of exosomes isolated from mouse embryonic fibroblasts in mice created as a sciatic nerve crush injury model},
journal = {Molecular Biology Reports},
year = {2024},
volume = {51},
publisher = {Springer Nature},
month = {oct},
url = {https://link.springer.com/10.1007/s11033-024-09962-z},
number = {1},
pages = {1046},
doi = {10.1007/s11033-024-09962-z}
}