Related Experiment Video
Updated: Jan 7, 2026

Cell-based Assay Protocol for the Prognostic Prediction of Idiopathic Scoliosis Using Cellular Dielectric Spectroscopy
Published on: October 16, 2013
Primary cilia gene defects in BMSCs induce idiopathic scoliosis
Li Zhang1, Wenhui Yang2, Zhi Zhao3
1Department of Orthopaedics, The 2nd Affiliated Hospital of Kunming Medical University, 374# Dianmian Road, Kunming, Yunnan Province, 6500101, People's Republic of China.
Abstract:
This paper investigated the role of cilia gene defects in bone marrow stem cells (BMSCs) in idiopathic scoliosis (IS). IS, a spinal deformity commonly occurring in adolescence, impacts patients' quality of life. Cilia, axial filaments covered by the cell membrane and composed of microtubules on the eukaryotic cell surface, include motile cilia and primary cilia. Primary cilia on the surface of most cells mediate intracellular signaling pathways. Cilia dysfunction correlates with skeletal diseases. Defects in cilia genes disrupt osteogenic signaling pathways in BMSCs, promoting IS progression. By sample analysis, lentiviral transfection of BMSCs, and in vivo experiments in zebrafish, we explored the impact of cilia gene defects on BMSCs' osteogenic signaling pathways and IS, revealing that defects impaired ciliogenesis, cellular signaling, and mechanical sensing, and affected vertebral alignment and skeletal patterning. These findings highlight the role of cilia gene defects in IS pathology, providing potential targets for clinical treatment.
Related Concept Videos
Microtubules in Signaling
Pedigree Analysis
Induced Pluripotent Stem Cells
Somatic...
Mechanism of Ciliary Motion
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
Satellite Stem Cells and Muscular Dystrophy
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...

