دورية أكاديمية

Specific targeting of inflammatory osteoclastogenesis by the probiotic yeast S. boulardii CNCM I-745 reduces bone loss in osteoporosis

التفاصيل البيبلوغرافية
العنوان: Specific targeting of inflammatory osteoclastogenesis by the probiotic yeast S. boulardii CNCM I-745 reduces bone loss in osteoporosis
المؤلفون: Madel, Maria Bernadette, Halper, Julia, Ibáñez, Lidia, Claire, Lozano, Rouleau, Matthieu, Boutin, Antoine, Mahler, Adrien, Pontier-Bres, Rodolphe, Ciucci, Thomas, Topi, Majlinda, Hue, Christophe, Amiaud, Jérôme, Iborra, Salvador, Sancho, David, Heymann, Dominique, Garchon, Henri Jean, Czerucka, Dorota, Apparailly, Florence, Duroux-Richard, Isabelle, Wakkach, Abdelilah, Blin-Wakkach, Claudine
المساهمون: Infection et inflammation (2I), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Ambroise Paré AP-HP, ANR-16-CE14-0030 Henri-Jean Garchon Henri-Jean GarchonFondation pour la Recherche Médicale ECO20160736019 Maria-Bernadette MadelAgence Nationale de la Recherche, Laboratory of Biochemistry-Hormonology, Société Française de Biologie des Tissus Minéralisés, Société Française de Rhumatol-ogie, UFR Simone Veil, Université Versailles-Saint-Quentin, Univer-sité Versailles-Saint-Quentin, National Institutes of Health, NIH, National Cancer Institute, NCI, Fondation Arthritis, American Society for Bone and Mineral Research, ASBMR, European Calcified Tissue Society, ECTS, Agence Nationale de la Recherche, ANR, (ANR-15-IDEX-01, ANR-16-CE14-0030), Fondation pour la Recherche Médicale, FRM, (ECO20160736019), Chung Hua University, CHU, (LP2M), Conseil Régional Provence-Alpes-Côte d'Azur, Société Française d'Hématologie, SFH, ANR-16-CE14-0030,ORIOS,Origine et rôle des ostéoclastes inflammatoires, nouvelles cibles thérapeutiques dans les maladies rhumatoïdes(2016)
المصدر: EISSN: 2050-084X ; eLife ; https://hal.science/hal-04068580Test ; eLife, 2023, 12, ⟨10.7554/eLife.82037⟩
بيانات النشر: HAL CCSD
eLife Sciences Publication
سنة النشر: 2023
المجموعة: Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQ
مصطلحات موضوعية: [SDV]Life Sciences [q-bio]
الوصف: International audience ; Bone destruction is a hallmark of chronic inflammation, and bone-resorbing osteoclasts arising under such a condition differ from steady-state ones. However, osteoclast diversity remains poorly explored. Here, we combined transcriptomic profiling, differentiation assays and in vivo analysis in mouse to decipher specific traits for inflammatory and steady-state osteoclasts. We identified and validated the pattern-recognition receptors (PRR) Tlr2, Dectin-1, and Mincle, all involved in yeast recognition as major regulators of inflammatory osteoclasts. We showed that administration of the yeast probiotic Saccharomyces boulardii CNCM I-745 (Sb) in vivo reduced bone loss in ovariectomized but not sham mice by reducing inflammatory osteoclastogenesis. This beneficial impact of Sb is mediated by the regulation of the inflammatory environment required for the generation of inflammatory osteoclasts. We also showed that Sb derivatives as well as agonists of Tlr2, Dectin-1, and Mincle specifically inhibited directly the differentiation of inflammatory but not steady-state osteoclasts in vitro. These findings demonstrate a preferential use of the PRR-associated costimulatory differentiation pathway by inflammatory osteoclasts, thus enabling their specific inhibition, which opens new therapeutic perspectives for inflammatory bone loss.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36848406; hal-04068580; https://hal.science/hal-04068580Test; https://hal.science/hal-04068580/documentTest; https://hal.science/hal-04068580/file/elife-82037-v1.pdfTest; PUBMED: 36848406
DOI: 10.7554/eLife.82037
الإتاحة: https://doi.org/10.7554/eLife.82037Test
https://hal.science/hal-04068580Test
https://hal.science/hal-04068580/documentTest
https://hal.science/hal-04068580/file/elife-82037-v1.pdfTest
حقوق: info:eu-repo/semantics/OpenAccess
رقم الانضمام: edsbas.B10F7060
قاعدة البيانات: BASE