$\require{mediawiki-texvc}$

연합인증

연합인증 가입 기관의 연구자들은 소속기관의 인증정보(ID와 암호)를 이용해 다른 대학, 연구기관, 서비스 공급자의 다양한 온라인 자원과 연구 데이터를 이용할 수 있습니다.

이는 여행자가 자국에서 발행 받은 여권으로 세계 각국을 자유롭게 여행할 수 있는 것과 같습니다.

연합인증으로 이용이 가능한 서비스는 NTIS, DataON, Edison, Kafe, Webinar 등이 있습니다.

한번의 인증절차만으로 연합인증 가입 서비스에 추가 로그인 없이 이용이 가능합니다.

다만, 연합인증을 위해서는 최초 1회만 인증 절차가 필요합니다. (회원이 아닐 경우 회원 가입이 필요합니다.)

연합인증 절차는 다음과 같습니다.

최초이용시에는
ScienceON에 로그인 → 연합인증 서비스 접속 → 로그인 (본인 확인 또는 회원가입) → 서비스 이용

그 이후에는
ScienceON 로그인 → 연합인증 서비스 접속 → 서비스 이용

연합인증을 활용하시면 KISTI가 제공하는 다양한 서비스를 편리하게 이용하실 수 있습니다.

Tal1 regulates osteoclast differentiation through suppression of the master regulator of cell fusion DC‐STAMP

The FASEB journal : official publication of the Federation of American Societies for Experimental Biology, v.26 no.2, 2012년, pp.523 - 532  

Courtial, Nadine (Georg‐) ,  Smink, Jeske J. (Speyer‐) ,  Kuvardina, Olga N. (HausInstitute for Biomedical Research Frankfurt Germany) ,  Leutz, Achim (Max‐) ,  Göthert, Joachim R. (Delbrü) ,  Lausen, Jörn (ck‐)

Abstract AI-Helper 아이콘AI-Helper

The balance between bone-forming osteoblasts and bone-resorbing osteoclasts is crucial to bone homeostasis, an equilibrium that is disturbed in many bone diseases. The transcription factor Tal1 is involved in the establishment of hematopoietic stem cells in the embryo and is a master regulator of he...

참고문헌 (58)

  1. Karsenty, Gerard, Wagner, Erwin F.. Reaching a Genetic and Molecular Understanding of Skeletal Development. Developmental cell, vol.2, no.4, 389-406.

  2. Zaidi, Mone. Skeletal remodeling in health and disease. Nature medicine, vol.13, no.7, 791-801.

  3. Boyle, William J., Simonet, W. Scott, Lacey, David L.. Osteoclast differentiation and activation. Nature, vol.423, no.6937, 337-342.

  4. Sambrook, Philip, Cooper, Cyrus. Osteoporosis. The Lancet, vol.367, no.9527, 2010-2018.

  5. Novack, Deborah V., Teitelbaum, Steven L.. The Osteoclast: Friend or Foe?. Annual review of pathology : mechanisms of disease, vol.3, 457-484.

  6. Helfrich, Miep H.. Osteoclast diseases. Microscopy research and technique, vol.61, no.6, 514-532.

  7. J. Musculoskelet. Neuronal Interact. Yavropoulou M. P. 204 8 2008 Osteoclastogenesis- current knowledge and future perspectives 

  8. Teitelbaum, Steven L., Ross, F. Patrick. Genetic regulation of osteoclast development and function. Nature reviews. Genetics, vol.4, no.8, 638-649.

  9. Asagiri, M., Takayanagi, H.. The molecular understanding of osteoclast differentiation. Bone, vol.40, no.2, 251-264.

  10. 10.1101/gad.13.18.2412 

  11. Kong, Young-Yun, Yoshida, Hiroki, Sarosi, Ildiko, Tan, Hong-Lin, Timms, Emma, Capparelli, Casey, Morony, Sean, Oliveira-dos-Santos, Antonio J., Van, Gwyneth, Itie, Annick, Khoo, Wilson, Wakeham, Andrew, Dunstan, Colin R., Lacey, David L., Mak, Tak W., Boyle, William J., Penninger, Josef M.. OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis. Nature, vol.397, no.6717, 315-323.

  12. Takayanagi, Hiroshi, Kim, Sunhwa, Koga, Takako, Nishina, Hiroshi, Isshiki, Masashi, Yoshida, Hiroki, Saiura, Akio, Isobe, Miho, Yokochi, Taeko, Inoue, Jun-ichiro, Wagner, Erwin F., Mak, Tak W., Kodama, Tatsuhiko, Taniguchi, Tadatsugu. Induction and Activation of the Transcription Factor NFATc1 (NFAT2) Integrate RANKL Signaling in Terminal Differentiation of Osteoclasts. Developmental cell, vol.3, no.6, 889-901.

  13. Ishida, Norihiro, Hayashi, Koji, Hoshijima, Mitsuhiro, Ogawa, Takuya, Koga, Shintaro, Miyatake, Yuuki, Kumegawa, Masayoshi, Kimura, Toru, Takeya, Tatsuo. Large Scale Gene Expression Analysis of Osteoclastogenesisin Vitro and Elucidation of NFAT2 as a Key Regulator. The Journal of biological chemistry, vol.277, no.43, 41147-41156.

  14. Asagiri, Masataka, Sato, Kojiro, Usami, Takako, Ochi, Sae, Nishina, Hiroshi, Yoshida, Hiroki, Morita, Ikuo, Wagner, Erwin F., Mak, Tak W., Serfling, Edgar, Takayanagi, Hiroshi. Autoamplification of NFATc1 expression determines its essential role in bone homeostasis. The Journal of experimental medicine, vol.202, no.9, 1261-1269.

  15. Kim, Kabsun, Kim, Jung Ha, Lee, Junwon, Jin, Hye Mi, Kook, Hyun, Kim, Kyung Keun, Lee, Soo Young, Kim, Nacksung. MafB negatively regulates RANKL-mediated osteoclast differentiation. Blood, vol.109, no.8, 3253-3259.

  16. Smink, Jeske J, Bégay, Valérie, Schoenmaker, Ton, Sterneck, Esta, de Vries, Teun J, Leutz, Achim. Transcription factor C/EBPβ isoform ratio regulates osteoclastogenesis through MafB. The EMBO journal, vol.28, no.12, 1769-1781.

  17. Luchin, Alexander, Suchting, Steven, Merson, Tobias, Rosol, Thomas J., Hume, David A., Cassady, A. Ian, Ostrowski, Michael C.. Genetic and Physical Interactions betweenMicrophthalmia Transcription Factor and PU.1 Are Necessary for Osteoclast Gene Expression and Differentiation. The Journal of biological chemistry, vol.276, no.39, 36703-36710.

  18. Motyckova, G., Weilbaecher, K. N., Horstmann, M., Rieman, D. J., Fisher, D. Z., Fisher, D. E.. Linking osteopetrosis and pycnodysostosis: Regulation of cathepsin K expression by the microphthalmia transcription factor family. Proceedings of the National Academy of Sciences of the United States of America, vol.98, no.10, 5798-5803.

  19. Matsumoto, Masahito, Kogawa, Masakazu, Wada, Seiki, Takayanagi, Hiroshi, Tsujimoto, Masafumi, Katayama, Shigehiro, Hisatake, Koji, Nogi, Yasuhisa. Essential Role of p38 Mitogen-activated Protein Kinase in Cathepsin K Gene Expression during Osteoclastogenesis through Association of NFATc1 and PU.1. The Journal of biological chemistry, vol.279, no.44, 45969-45979.

  20. Kim, Kabsun, Lee, Seoung-Hoon, Ha Kim, Jung, Choi, Yongwon, Kim, Nacksung. NFATc1 Induces Osteoclast Fusion Via Up-Regulation of Atp6v0d2 and the Dendritic Cell-Specific Transmembrane Protein (DC-STAMP). Molecular endocrinology, vol.22, no.1, 176-185.

  21. Ishii, Masaru, Saeki, Yukihiko. Osteoclast cell fusion: mechanisms and molecules. Modern Rheumatology, vol.18, no.3, 220-227.

  22. Yagi, Mitsuru, Miyamoto, Takeshi, Sawatani, Yumi, Iwamoto, Katsuya, Hosogane, Naobumi, Fujita, Nobuyuki, Morita, Kozo, Ninomiya, Ken, Suzuki, Toru, Miyamoto, Kana, Oike, Yuichi, Takeya, Motohiro, Toyama, Yoshiaki, Suda, Toshio. DC-STAMP is essential for cell–cell fusion in osteoclasts and foreign body giant cells. The Journal of experimental medicine, vol.202, no.3, 345-351.

  23. Kukita, Toshio, Wada, Naohisa, Kukita, Akiko, Kakimoto, Takashi, Sandra, Ferry, Toh, Kazuko, Nagata, Kengo, Iijima, Tadahiko, Horiuchi, Madoka, Matsusaki, Hiromi, Hieshima, Kunio, Yoshie, Osamu, Nomiyama, Hisayuki. RANKL-induced DC-STAMP Is Essential for Osteoclastogenesis. The Journal of experimental medicine, vol.200, no.7, 941-946.

  24. Bloor, Adrian J.C., Sánchez, María-José, Green, Anthony R., Göttgens, Berthold. The Role of the Stem Cell Leukemia (SCL) Gene in Hematopoietic and Endothelial Lineage Specification. Journal of hematotherapy & stem cell research, vol.11, no.2, 195-206.

  25. Lécuyer, Eric, Hoang, Trang. SCL: From the origin of hematopoiesis to stem cells and leukemia. Experimental hematology, vol.32, no.1, 11-24.

  26. Shivdasani, Ramesh A., Mayer, Erica L., Orkin, Stuart H.. Absence of blood formation in mice lacking the T-cell leukaemia oncoprotein tal-1/SCL. Nature, vol.373, no.6513, 432-434.

  27. Robb, L, Lyons, I, Li, R, Hartley, L, Köntgen, F, Harvey, R P, Metcalf, D, Begley, C G. Absence of yolk sac hematopoiesis from mice with a targeted disruption of the scl gene.. Proceedings of the National Academy of Sciences of the United States of America, vol.92, no.15, 7075-7079.

  28. Hall, Mark A., Curtis, David J., Metcalf, Donald, Elefanty, Andrew G., Sourris, K., Robb, Lorraine, Göthert, Joachim R., Jane, Stephen M., Begley, C. Glenn. The critical regulator of embryonic hematopoiesis, SCL, is vital in the adult for megakaryopoiesis, erythropoiesis, and lineage choice in CFU-S 12. Proceedings of the National Academy of Sciences of the United States of America, vol.100, no.3, 992-997.

  29. Huang, Suming, Brandt, Stephen J.. mSin3A Regulates Murine Erythroleukemia Cell Differentiation through Association with the TAL1 (or SCL) Transcription Factor. Molecular and cellular biology, vol.20, no.6, 2248-2259.

  30. Huang, Suming, Qiu, Yi, Stein, Roland W, Brandt, Stephen J. p300 functions as a transcriptional coactivator for the TAL1/SCL oncoprotein. Oncogene, vol.18, no.35, 4958-4967.

  31. Yamane, Toshiyuki, Kunisada, Takahiro, Yamazaki, Hidetoshi, Nakano, Toru, Orkin, Stuart H, Hayashi, Shin-Ichi. Sequential requirements for SCL/tal-1, GATA-2, macrophage colony-stimulating factor, and osteoclast differentiation factor/osteoprotegerin ligand in osteoclast development. Experimental hematology, vol.28, no.7, 833-840.

  32. Weischenfeldt, Joachim, Porse, Bo. Bone Marrow-Derived Macrophages (BMM): Isolation and Applications. CSH protocols, vol.2008, no.12, pdb.prot5080-.

  33. Demaison, Christophe, Parsley, Kathryn, Brouns, Gaby, Scherr, Michaela, Battmer, Karin, Kinnon, Christine, Grez, Manuel, Thrasher, Adrian J.. High-Level Transduction and Gene Expression in Hematopoietic Repopulating Cells Using a Human Imunodeficiency Virus Type 1-Based Lentiviral Vector Containing an Internal Spleen Focus Forming Virus Promoter. Human gene therapy, vol.13, no.7, 803-813.

  34. Weber, Kristoffer, Bartsch, Udo, Stocking, Carol, Fehse, Boris. A Multicolor Panel of Novel Lentiviral “Gene Ontology” (LeGO) Vectors for Functional Gene Analysis. Molecular therapy : the journal of the American Society of Gene Therapy, vol.16, no.4, 698-706.

  35. Ida-Yonemochi, Hiroko, Ishibashi, Osamu, Sakai, Hideaki, Saku, Takashi. Recruitment of osteoclasts in the mandible of osteopetrotic (op/op) mice. European journal of oral sciences, vol.112, no.2, 148-155.

  36. Smink, J.J, Buchholz, I.M, Hamers, N, van Tilburg, C.M, Christis, C, Sakkers, R.J.B, de Meer, K, van Buul-Offers, S.C, Koedam, J.A. Short-term glucocorticoid treatment of piglets causes changes in growth plate morphology and angiogenesis. Osteoarthritis and cartilage, vol.11, no.12, 864-871.

  37. Yagi, Mitsuru, Ninomiya, Ken, Fujita, Nobuyuki, Suzuki, Toru, Iwasaki, Ryotaro, Morita, Kozo, Hosogane, Naobumi, Matsuo, Koichi, Toyama, Yoshiaki, Suda, Toshio, Miyamoto, Takeshi. Induction of DC-STAMP by Alternative Activation and Downstream Signaling Mechanisms. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol.22, no.7, 992-1001.

  38. Elefanty, Andrew G., Begley, C. Glenn, Metcalf, Donald, Barnett, Louise, Köntgen, Frank, Robb, Lorraine. Characterization of hematopoietic progenitor cells that express the transcription factor SCL, using a lacZ “knock-in” strategy. Proceedings of the National Academy of Sciences of the United States of America, vol.95, no.20, 11897-11902.

  39. Jacquin, Claire, Gran, Diane E, Lee, Sun Kyeong, Lorenzo, Joseph A, Aguila, Hector L. Identification of Multiple Osteoclast Precursor Populations in Murine Bone Marrow. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol.21, no.1, 67-77.

  40. Huang, Da Wei, Sherman, Brad T, Lempicki, Richard A. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nature protocols, vol.4, no.1, 44-57.

  41. Cell Stem Cell Wilson N. K. 532 10.1016/j.stem.2010.07.016 7 Combinatorial transcriptional control in blood stem/progenitor cells: genome­wide analysis of ten major transcriptional regulators 

  42. Pimanda, John E., Silberstein, Lev, Dominici, Massimo, Dekel, Benjamin, Bowen, Mark, Oldham, Scott, Kallianpur, Asha, Brandt, Stephen J., Tannahill, David, Göttgens, Berthold, Green, Anthony R.. Transcriptional Link between Blood and Bone: the Stem Cell Leukemia Gene and Its +19 Stem Cell Enhancer Are Active in Bone Cells. Molecular and cellular biology, vol.26, no.7, 2615-2625.

  43. Arnold, Michael A., Kim, Yuri, Czubryt, Michael P., Phan, Dillon, McAnally, John, Qi, Xiaoxia, Shelton, John M., Richardson, James A., Bassel-Duby, Rhonda, Olson, Eric N.. MEF2C Transcription Factor Controls Chondrocyte Hypertrophy and Bone Development. Developmental cell, vol.12, no.3, 377-389.

  44. Gekas, Christos, Rhodes, Katrin E., Gereige, Laurraine M., Helgadottir, Hildur, Ferrari, Roberto, Kurdistani, Siavash K., Montecino-Rodriguez, Encarnación, Bassel-Duby, Rhonda, Olson, Eric, Krivtsov, Andrei V., Armstrong, Scott, Orkin, Stuart H., Pellegrini, Matteo, Mikkola, Hanna K. A.. Mef2C is a lineage-restricted target of Scl/Tal1 and regulates megakaryopoiesis and B-cell homeostasis. Blood, vol.113, no.15, 3461-3471.

  45. Dey, Soumyadeep, Curtis, David J., Jane, Stephen M., Brandt, Stephen J.. The TAL1/SCL Transcription Factor Regulates Cell Cycle Progression and Proliferation in Differentiating Murine Bone Marrow Monocyte Precursors. Molecular and cellular biology, vol.30, no.9, 2181-2192.

  46. Blood Pulford K. 675 85 1995 10.1182/blood.V85.3.675.bloodjournal853675 Expression of TAL­1 proteins in human tissues 

  47. Terme, Jean-Michel, Lhermitte, Ludovic, Asnafi, Vahid, Jalinot, Pierre. TGF-β induces degradation of TAL1/SCL by the ubiquitin-proteasome pathway through AKT-mediated phosphorylation. Blood, vol.113, no.26, 6695-6698.

  48. Nie, Lei, Wu, Huaqing, Sun, Xiao-Hong. Ubiquitination and Degradation of Tal1/SCL Are Induced by Notch Signaling and Depend on Skp2 and CHIP. The Journal of biological chemistry, vol.283, no.2, 684-692.

  49. Mizoguchi, Fumitaka, Izu, Yayoi, Hayata, Tadayoshi, Hemmi, Hiroaki, Nakashima, Kazuhisa, Nakamura, Takashi, Kato, Shigeaki, Miyasaka, Nobuyuki, Ezura, Yoichi, Noda, Masaki. Osteoclast-specific Dicer gene deficiency suppresses osteoclastic bone resorption. Journal of cellular biochemistry, vol.109, no.5, 866-875.

  50. Sugatani, Toshifumi, Hruska, Keith A.. Impaired Micro-RNA Pathways Diminish Osteoclast Differentiation and Function. The Journal of biological chemistry, vol.284, no.7, 4667-4678.

  51. Sugatani, Toshifumi, Vacher, Jean, Hruska, Keith A.. A microRNA expression signature of osteoclastogenesis. Blood, vol.117, no.13, 3648-3657.

  52. Helming, L., Gordon, S.. Molecular mediators of macrophage fusion. Trends in cell biology, vol.19, no.10, 514-522.

  53. J. Cell. Physiol. Mensah K. A. 76 223 RANKL induces heterogeneous DC­STAMP(lo) and DC­STAMP(hi) osteoclast precursors of which the DC­STAMP(lo) precursors are the master fusogens 

  54. Yagi, Mitsuru, Miyamoto, Takeshi, Toyama, Yoshiaki, Suda, Toshio. Role of DC-STAMP in cellular fusion of osteoclasts and macrophage giant cells. Journal of bone and mineral metabolism, vol.24, no.5, 355-358.

  55. Tsuneto, Motokazu, Tominaga, Akira, Yamazaki, Hidetoshi, Yoshino, Miya, Orkin, Stuart H., Hayashi, Shin-Ichi. Enforced Expression of PU.1 Rescues Osteoclastogenesis from Embryonic Stem Cells Lacking Tal-1. Stem cells®, vol.23, no.1, 134-143.

  56. Hu, Rong, Sharma, Sudarshana M., Bronisz, Agnieszka, Srinivasan, Ruchika, Sankar, Uma, Ostrowski, Michael C.. Eos, MITF, and PU.1 Recruit Corepressors to Osteoclast-Specific Genes in Committed Myeloid Progenitors. Molecular and cellular biology, vol.27, no.11, 4018-4027.

  57. Anract, P., De Pinieux, G., Cottias, P., Pouillart, P., Forest, M., Tomeno, B.. Malignant giant-cell tumours of bone. International orthopaedics, vol.22, no.1, 19-26.

  58. Campanacci, M, Baldini, N, Boriani, S, Sudanese, A. Giant-cell tumor of bone. :. Journal of bone and joint surgery : American volume, vol.69, no.1, 106-114.

섹션별 컨텐츠 바로가기

AI-Helper ※ AI-Helper는 오픈소스 모델을 사용합니다.

AI-Helper 아이콘
AI-Helper
안녕하세요, AI-Helper입니다. 좌측 "선택된 텍스트"에서 텍스트를 선택하여 요약, 번역, 용어설명을 실행하세요.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.

선택된 텍스트

맨위로