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1.
Commun Biol ; 2: 86, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30854478

RESUMO

Osteoclasts are multinucleated cells responsible for bone resorption. The differentiation of osteoclasts from bone marrow macrophages (BMMs) is induced by receptor activator of NF-κB ligand (RANKL). Osteoprotegerin (OPG), a decoy receptor of RANKL, inhibits osteoclastogenesis by blocking RANKL signaling. Here we investigated the degradation of OPG in vitro. Osteoclasts, but not BMMs, secreted OPG-degrading enzymes. Using mass spectrometry and RNA-sequencing analysis, we identified high-temperature requirement A serine peptidase 1 (HtrA1) as an OPG-degrading enzyme. HtrA1 did not degrade OPG pre-reduced by dithiothreitol, suggesting that HtrA1 recognizes the three-dimensional structure of OPG. HtrA1 initially cleaved the amide bond between leucine 90 and glutamine 91 of OPG, then degraded OPG into small fragments. Inhibitory activity of OPG on RANKL-induced osteoclastogenesis was suppressed by adding HtrA1 in RAW 264.7 cell cultures. These results suggest that osteoclasts potentially prepare a microenvironment suitable for osteoclastogenesis. HtrA1 may be a novel drug target for osteoporosis.


Assuntos
Osso e Ossos/metabolismo , Microambiente Celular , Serina Peptidase 1 de Requerimento de Alta Temperatura A/metabolismo , Osteoclastos/metabolismo , Osteoprotegerina/metabolismo , Animais , Células da Medula Óssea/metabolismo , Diferenciação Celular , Células Cultivadas , Microambiente Celular/genética , Serina Peptidase 1 de Requerimento de Alta Temperatura A/genética , Macrófagos/metabolismo , Metaloproteinase 9 da Matriz/metabolismo , Camundongos , Osteoblastos/metabolismo , Osteogênese/genética , Osteoprotegerina/genética , Proteólise , Análise de Sequência de RNA
3.
J Biomed Semantics ; 4(1): 6, 2013 Feb 11.
Artigo em Inglês | MEDLINE | ID: mdl-23398680

RESUMO

BACKGROUND: BioHackathon 2010 was the third in a series of meetings hosted by the Database Center for Life Sciences (DBCLS) in Tokyo, Japan. The overall goal of the BioHackathon series is to improve the quality and accessibility of life science research data on the Web by bringing together representatives from public databases, analytical tool providers, and cyber-infrastructure researchers to jointly tackle important challenges in the area of in silico biological research. RESULTS: The theme of BioHackathon 2010 was the 'Semantic Web', and all attendees gathered with the shared goal of producing Semantic Web data from their respective resources, and/or consuming or interacting those data using their tools and interfaces. We discussed on topics including guidelines for designing semantic data and interoperability of resources. We consequently developed tools and clients for analysis and visualization. CONCLUSION: We provide a meeting report from BioHackathon 2010, in which we describe the discussions, decisions, and breakthroughs made as we moved towards compliance with Semantic Web technologies - from source provider, through middleware, to the end-consumer.

4.
Calcif Tissue Int ; 86(1): 47-57, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19921088

RESUMO

Osteoarthritis (OA) is the most prevalent joint disease and is characterized by pain and functional loss of the joint. However, the pathogenic mechanism of OA remains unclear, and no drug therapy for preventing its progress has been established. To identify genes related to the progress of OA, the gene expression profiles of paired intact and damaged cartilage obtained from OA patients undergoing joint substitution were compared using oligo microarrays. Using functional categorization combined with gene ontology and a statistical analysis, five genes were found to be highly expressed in damaged cartilage (HBEGF, ASUS, CRLF1, LOX, CDA), whereas three genes were highly expressed in intact tissues (CHST2, PTPRD, CPAN6). Among these genes, the upregulated expression of CRLF1 was reconfirmed using real-time PCR, and the in vivo expression of CRLF1 was detected in clusters of chondrocytes and fibrocartilage-like cells in damaged OA cartilages using in situ hybridization. In vitro, the transcriptional level of CRLF1 was positively regulated by TGF-beta1 in the mouse chondrogenic cell line ATDC5. Additionally, the CRLF1/CLC complex promoted the proliferation of ATDC5 cells and suppressed the expression level of aggrecan and type II collagen. Our data suggest that the CRLF1/CLC complex disrupts cartilage homeostasis and promotes the progress of OA by enhancing the proliferation of chondrocytes and suppressing the production of cartilage matrix. A component of the complex, CRLF1, may be useful as a biomarker of OA; and the corresponding receptor is a potential new drug target for OA.


Assuntos
Cartilagem Articular/metabolismo , Articulação do Joelho/metabolismo , Osteoartrite do Joelho/metabolismo , Receptores de Citocinas/genética , Transdução de Sinais/fisiologia , Fator de Crescimento Transformador beta/genética , Agrecanas/metabolismo , Animais , Biomarcadores/análise , Biomarcadores/metabolismo , Cartilagem Articular/imunologia , Cartilagem Articular/fisiopatologia , Linhagem Celular , Proliferação de Células , Condrócitos/metabolismo , Colágeno Tipo II/metabolismo , Proteínas da Matriz Extracelular/genética , Regulação da Expressão Gênica/fisiologia , Humanos , Articulação do Joelho/imunologia , Articulação do Joelho/fisiopatologia , Camundongos , Análise de Sequência com Séries de Oligonucleotídeos , Osteoartrite do Joelho/imunologia , Osteoartrite do Joelho/fisiopatologia , RNA Mensageiro/análise , RNA Mensageiro/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Ativação Transcricional/genética , Regulação para Cima/genética
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