{"title":"NF-.KAPPA.B(RANK)胞外结构域受体激活因子的功能表征。","authors":"T. Imai, M. Shibata, A. Mizuno, Y. Kato","doi":"10.2330/JORALBIOSCI1965.45.130","DOIUrl":null,"url":null,"abstract":"Receptor activator of NF-kB (RANK) and its ligand, receptor activator of NF-kB ligand (RANKL) play a crucial role in the differentiation and activation of osteoclasts. In order to evaluate the efficacy of RANK, we designed a soluble murine RANK (sRANK) and compared its functional activitywith Osteoprotegerin (OPG), a soluble decoy receptor for RANKL. sRANK was expressed in baculovirus-infected Sf-9 cells and purified by Ni-NTA chromatography followed by MonoQ column elution. The binding affinity of the purified sRANK to RANKL was quite similar to that of OPG. Furthermore, the inhibitory effect on RANKL-induced osteoclastogenesis from mouse bone marrow cells showed no significant difference between sRANK and OPG. However, sRANK had no effect on TNF-related apoptosisinducing ligand (TRAIL) -induced apoptosis, although OPG prevented the cytotoxic activity of TRAIL. The results of this study suggest that recombinant sRANK may have therapeutic value as an inhibitor of bone resorption.","PeriodicalId":14631,"journal":{"name":"Japanese Journal of Oral Biology","volume":"2 1","pages":"130-138"},"PeriodicalIF":0.0000,"publicationDate":"2003-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Functional Characterization of the Receptor Activator of NF-.KAPPA.B(RANK) Extracellular Domain.\",\"authors\":\"T. Imai, M. Shibata, A. Mizuno, Y. Kato\",\"doi\":\"10.2330/JORALBIOSCI1965.45.130\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Receptor activator of NF-kB (RANK) and its ligand, receptor activator of NF-kB ligand (RANKL) play a crucial role in the differentiation and activation of osteoclasts. In order to evaluate the efficacy of RANK, we designed a soluble murine RANK (sRANK) and compared its functional activitywith Osteoprotegerin (OPG), a soluble decoy receptor for RANKL. sRANK was expressed in baculovirus-infected Sf-9 cells and purified by Ni-NTA chromatography followed by MonoQ column elution. The binding affinity of the purified sRANK to RANKL was quite similar to that of OPG. Furthermore, the inhibitory effect on RANKL-induced osteoclastogenesis from mouse bone marrow cells showed no significant difference between sRANK and OPG. However, sRANK had no effect on TNF-related apoptosisinducing ligand (TRAIL) -induced apoptosis, although OPG prevented the cytotoxic activity of TRAIL. The results of this study suggest that recombinant sRANK may have therapeutic value as an inhibitor of bone resorption.\",\"PeriodicalId\":14631,\"journal\":{\"name\":\"Japanese Journal of Oral Biology\",\"volume\":\"2 1\",\"pages\":\"130-138\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-06-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Japanese Journal of Oral Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2330/JORALBIOSCI1965.45.130\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese Journal of Oral Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2330/JORALBIOSCI1965.45.130","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
NF-kB受体激活因子(Receptor activator of NF-kB, RANK)及其配体,NF-kB配体受体激活因子(Receptor activator of NF-kB, RANKL)在破骨细胞的分化和活化中起着至关重要的作用。为了评价RANK的有效性,我们设计了一种可溶性小鼠RANK (sRANK),并将其与RANKL的可溶性诱饵受体骨保护素(OPG)的功能活性进行了比较。sRANK在杆状病毒感染的Sf-9细胞中表达,经Ni-NTA层析和MonoQ柱洗脱纯化。纯化后的sRANK与RANKL的结合亲和力与OPG非常相似。此外,对rankl诱导的小鼠骨髓细胞破骨细胞生成的抑制作用在rankl和OPG之间没有显著差异。然而,尽管OPG可以阻止TRAIL的细胞毒活性,但sRANK对tnf相关的凋亡诱导配体(TRAIL)诱导的细胞凋亡没有影响。本研究结果提示重组sRANK作为骨吸收抑制剂可能具有治疗价值。
Functional Characterization of the Receptor Activator of NF-.KAPPA.B(RANK) Extracellular Domain.
Receptor activator of NF-kB (RANK) and its ligand, receptor activator of NF-kB ligand (RANKL) play a crucial role in the differentiation and activation of osteoclasts. In order to evaluate the efficacy of RANK, we designed a soluble murine RANK (sRANK) and compared its functional activitywith Osteoprotegerin (OPG), a soluble decoy receptor for RANKL. sRANK was expressed in baculovirus-infected Sf-9 cells and purified by Ni-NTA chromatography followed by MonoQ column elution. The binding affinity of the purified sRANK to RANKL was quite similar to that of OPG. Furthermore, the inhibitory effect on RANKL-induced osteoclastogenesis from mouse bone marrow cells showed no significant difference between sRANK and OPG. However, sRANK had no effect on TNF-related apoptosisinducing ligand (TRAIL) -induced apoptosis, although OPG prevented the cytotoxic activity of TRAIL. The results of this study suggest that recombinant sRANK may have therapeutic value as an inhibitor of bone resorption.