Mesenchymal stem cell-based therapy for osteoporotic bones: Effects of the interaction between cells from healthy and osteoporotic rats on osteoblast differentiation and bone repair

• Published in: Life sciences (1973) 2024-03, Vol.340, p.122463-122463, Article 122463
• Main Authors: Souza, Alann Thaffarell Portilho, Freitas, Gileade Pereira, Lopes, Helena Bacha, Weffort, Denise, Adolpho, Leticia Faustino, Gomes, Maria Paula Oliveira, Oliveira, Fabiola Singaretti, Almeida, Adriana Luisa Gonçalves, Beloti, Marcio Mateus, Rosa, Adalberto Luiz
• Format: Article
• Language: English
• Subjects: Animal model; Animals; Bone and Bones - metabolism; bone formation; bone marrow; bone morphogenetic proteins; Bone regeneration; castration; Cell Differentiation - genetics; Cells, Cultured; coculture; femur; gene expression; histology; Humans; Mesenchymal Stem Cells; morphometry; osteoblasts; Osteoblasts - metabolism; Osteogenesis; Osteoporosis; Osteoporosis - metabolism; phenotype; Rats; Regenerative medicine; Stem cell
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2024.122463

Cell therapy utilizing mesenchymal stem cells (MSCs) from healthy donors (HE-MSCs) is a promising strategy for treating osteoporotic bone defects. This study investigated the effects of interaction between HE-MSCs and MSCs from osteoporotic donors (ORX-MSCs) on osteoblast differentiation of MSCs and of HE-MSCs on bone formation in calvarial defects of osteoporotic rats. Osteoporosis was induced by orchiectomy (ORX) and its effects on the bone were evaluated by femur microtomography (μCT) and osteoblast differentiation of bone marrow MSCs. HE- and ORX-MSCs were cocultured, and osteoblast differentiation was evaluated using genotypic and phenotypic parameters. HE-MSCs were injected into the calvarial defects of osteoporotic rats, and bone formation was evaluated by μCT, histology, and gene expression of osteoblast markers. ORX-induced osteoporosis was revealed by reduced bone morphometric parameters and osteoblast differentiation in ORX-MSCs. HE-MSCs partially recovered the osteogenic potential of ORX-MSCs, whereas HE-MSCs were mildly affected by ORX-MSCs. Additionally, the bone morphogenetic protein and wingless-related integration site signaling pathway components were similarly modulated in cocultures involving ORX-MSCs. HE-MSCs induced meaningful bone formation, highlighting the effectiveness of cell therapy even in osteoporotic bones. These results provide new perspectives on the development of cell-based therapies to regenerate bone defects in patients with disorders that affect bone tissue.