Protein phosphatase 2A Cα regulates osteoblast differentiation and the expressions of bone sialoprotein and osteocalcin via osterix transcription factor

التفاصيل البيبلوغرافية
العنوان: Protein phosphatase 2A Cα regulates osteoblast differentiation and the expressions of bone sialoprotein and osteocalcin via osterix transcription factor
المؤلفون: Tatsuji Haneji, Hirohiko Okamura, Di Yang, Kaya Yoshida
المصدر: Journal of cellular physiology. 228(5)
سنة النشر: 2012
مصطلحات موضوعية: Bone sialoprotein, Physiology, Cellular differentiation, Clinical Biochemistry, Osteocalcin, macromolecular substances, environment and public health, Mice, Osteogenesis, medicine, Animals, Integrin-Binding Sialoprotein, Protein Phosphatase 2, Sp7 Transcription Factor, Transcription factor, Cell Proliferation, biology, Chemistry, musculoskeletal, neural, and ocular physiology, Gene Expression Regulation, Developmental, Osteoblast, Cell Differentiation, Cell Biology, Protein phosphatase 2, 3T3 Cells, Cell biology, enzymes and coenzymes (carbohydrates), medicine.anatomical_structure, Biochemistry, embryonic structures, biology.protein, Alkaline phosphatase, Transcription Factors
الوصف: Serine/threonine protein phosphatase 2A (PP2A) participates in regulating many important physiological processes such as cell cycle, growth, apoptosis, and signal transduction. Osterix is a zinc-finger-containing transcription factor that is essential for osteoblast differentiation and regulation of many bone-related genes. We have recently reported that decrease in α-isoform of PP2A catalytic subunit (PP2A Cα) accelerates osteoblast differentiation through the expression of bone-related genes. In this study, we further examined the role of PP2A Cα in osteoblast differentiation by establishing the stable cell lines that overexpress PP2A Cα. Overexpression of PP2A Cα reduced alkaline phosphatase (ALP) activity. Osteoblast differentiation and mineralization were also decreased in PP2A Cα-overexpressing cells, with reduction of bone-related genes including osterix, bone sialoprotein (Bsp), and osteocalcin (OCN). Luciferase assay showed that the transcriptional activity of the Osterix promoter region was decreased in PP2A Cα-overexpressing cells. Introduction of ectopic Osterix rescued the expression of Bsp and OCN in PP2A Cα-overexpressing cells. These results indicate that PP2A Cα and its activity play a negative role in osteoblast differentiation and Osterix is a key factor responsible for regulating the expressions of Bsp and OCN during PP2A Cα-mediated osteoblast differentiation.
تدمد: 1097-4652
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::254b3a40d5a345048c90e25ae61c442dTest
https://pubmed.ncbi.nlm.nih.gov/23042641Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....254b3a40d5a345048c90e25ae61c442d
قاعدة البيانات: OpenAIRE