Reference - Detail
| RRC ID | 43412 |
|---|---|
| Author | Shinoda Y, Ogata N, Higashikawa A, Manabe I, Shindo T, Yamada T, Kugimiya F, Ikeda T, Kawamura N, Kawasaki Y, Tsushima K, Takeda N, Nagai R, Hoshi K, Nakamura K, Chung UI, Kawaguchi H. |
| Title | Kruppel-like factor 5 causes cartilage degradation through transactivation of matrix metalloproteinase 9. |
| Journal | J Biol Chem |
| Abstract |
Although degradation of cartilage matrix has been suggested to be a rate-limiting step for endochondral ossification during skeletal development, little is known about the transcriptional regulation. This study investigated the involvement of KLF5 (Krüppel-like factor 5), an Sp/KLF family member, in the skeletal development. KLF5 was expressed in chondrocytes and osteoblasts but not in osteoclasts. The heterozygous deficient (KLF5+/-) mice exhibited skeletal growth retardation in the perinatal period. Although chondrocyte proliferation and differentiation were normal, cartilage matrix degradation was impaired in KLF5+/- mice, causing delay in replacement of cartilage with bone at the primary ossification center in the embryonic limbs and elongation of hypertrophic chondrocyte layer in the neonatal growth plates. Microarray analyses identified MMP9 (matrix metalloproteinase 9) as a transcriptional target, since it was strongly up-regulated by adenoviral transfection of KLF5 in chondrogenic cell line OUMS27. The KLF5 overexpression caused gelatin degradation by stimulating promoter activity of MMP9 without affecting chondrocyte differentiation or vascular endothelial growth factor expression in the culture of chondrogenic cells; however, in osteoclast precursors, it affected neither MMP9 expression nor osteoclastic differentiation. KLF5 dysfunction by genetic heterodeficiency or RNA interference was confirmed to cause reduction of MMP9 expression in cultured chondrogenic cells. MMP9 expression was decreased in the limbs of KLF5+/- embryos, which was correlated with suppression of matrix degradation, calcification, and vascularization. We conclude that KLF5 causes cartilage matrix degradation through transcriptional induction of MMP9, providing the first evidence that transcriptional regulation of a proteinase contributes to endochondral ossification and skeletal development. |
| Volume | 283(36) |
| Pages | 24682-9 |
| Published | 2008-9-5 |
| DOI | 10.1074/jbc.M709857200 |
| PII | S0021-9258(19)49214-4 |
| PMID | 18617520 |
| PMC | PMC3259811 |
| MeSH | Animals Cartilage / cytology Cartilage / embryology* Cell Differentiation / physiology Cell Line Cell Proliferation Chondrocytes / cytology Chondrocytes / metabolism* Extracellular Matrix / genetics Extracellular Matrix / metabolism Extremities / embryology Gene Expression Profiling Gene Expression Regulation, Developmental / physiology Humans Kruppel-Like Transcription Factors / genetics Kruppel-Like Transcription Factors / metabolism* Matrix Metalloproteinase 9 / biosynthesis* Matrix Metalloproteinase 9 / genetics Mice Oligonucleotide Array Sequence Analysis Organ Specificity / physiology Osteogenesis / physiology* Promoter Regions, Genetic / physiology RNA Interference Transcription, Genetic Transcriptional Activation / physiology* |
| IF | 4.238 |
| Times Cited | 31 |
| WOS Category | BIOCHEMISTRY & MOLECULAR BIOLOGY |
| Altmetric score |
オルトメトリクス指標項目
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| The most frequently cited source | Patent(IFI CLAIMS) |
| Total number of mentions | 6 |
| Altmetric score changes over past 6months | 0.0 |
| Resource | |
| Human and Animal Cells | ATDC5(RCB0565) MC3T3-E1(RCB1126) RAW 264(RCB0535) |