دورية أكاديمية

B. abortus Infection Promotes an Imbalance in the Adipocyte–Osteoblast Crosstalk Favoring Bone Resorption

التفاصيل البيبلوغرافية
العنوان: B. abortus Infection Promotes an Imbalance in the Adipocyte–Osteoblast Crosstalk Favoring Bone Resorption
المؤلفون: Rosa Nicole Freiberger, Cinthya Alicia Marcela López, Franco Agustín Sviercz, Cintia Cevallos, Alex David Guano, Patricio Jarmoluk, Jorge Quarleri, María Victoria Delpino
المصدر: International Journal of Molecular Sciences, Vol 24, Iss 6, p 5617 (2023)
بيانات النشر: MDPI AG, 2023.
سنة النشر: 2023
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: Brucella, adipocyte, osteoblast, IL-6, PPAR-γ, RUNX-2, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: Osteoarticular injury is the most common presentation of active brucellosis in humans. Osteoblasts and adipocytes originate from mesenchymal stem cells (MSC). Since those osteoblasts are bone-forming cells, the predilection of MSC to differentiate into adipocytes or osteoblasts is a potential factor involved in bone loss. In addition, osteoblasts and adipocytes can be converted into each other according to the surrounding microenvironment. Here, we study the incumbency of B. abortus infection in the crosstalk between adipocytes and osteoblasts during differentiation from its precursors. Our results indicate that soluble mediators present in culture supernatants from B. abotus-infected adipocytes inhibit osteoblast mineral matrix deposition in a mechanism dependent on the presence of IL-6 with the concomitant reduction of Runt-related transcription factor 2 (RUNX-2) transcription, but without altering organic matrix deposition and inducing nuclear receptor activator ligand kβ (RANKL) expression. Secondly, B. abortus-infected osteoblasts stimulate adipocyte differentiation with the induction of peroxisome proliferator-activated receptor γ (PPAR-γ) and CCAAT enhancer binding protein β (C/EBP-β). We conclude that adipocyte–osteoblast crosstalk during B. abortus infection could modulate mutual differentiation from its precursor cells, contributing to bone resorption.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 24065617
1422-0067
1661-6596
Relation: https://www.mdpi.com/1422-0067/24/6/5617; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067
DOI: 10.3390/ijms24065617
URL الوصول: https://doaj.org/article/c69226b14c1548439fe0fb21080b749c
رقم الأكسشن: edsdoj.69226b14c1548439fe0fb21080b749c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:24065617
14220067
16616596
DOI:10.3390/ijms24065617