TNFRSF 11 B ( tumor necrosis factor receptor superfamily , member 11 b )

نویسندگان

  • Maria Grazia Di Iasio
  • Federica Corallini
  • Paola Secchiero
  • Silvano Capitani
چکیده

Note RefSeq NP-002537.3; Size: 401 amino acids; 46040 Da; Subunit: Homodimer; Subcellular location: Secreted. Osteoprotegerin (OPG) was isolated independently by two laboratories in 1997 (Tsuda et al., 1997; Simonet et al., 1997), as being a protein that exhibits a protective effect on bone. OPG is a member of the TNF-receptor superfamily, which consists of proteins that evoke different signal transduction, mediating several biological responses, such as cytotoxicity, apoptosis and cell survival, proliferation and differentiation. OPG has two known TNF family ligands: receptor activator of NF-kB ligand (RANKL) (Yasuda et al., 1998b) and TRAIL (Emery et al., 1998) (Diagram 1). RANKL normally binds to its membrane receptor RANK inducing differentiation, activation, and survival of osteoclasts. By binding to RANKL, OPG acts as a soluble inhibitor that prevents RANKL/RANK interaction and subsequent osteoclastogenesis (Yasuda et al., 1998b) (Diagram 1). However, it has been reported that also OPG binding to TRAIL inhibits TRAIL/TRAIL-receptors (TR-R1/R2) interaction, as revealed by the inhibition of TRAIL-induced apoptosis (Emery et al., 1998) (Diagram 1). Vice-versa, TRAIL can block the inhibitory activity of OPG on osteoclastogenesis (Emery et al., 1998).

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

TNFRSF 6 B ( tumor necrosis factor receptor superfamily , member 6 b , decoy )

DNA sequence is located on chromosome 20. Transcription consists of 7 exons and 6 introns, spanning 3.6kb. A shorter transcription variance (M68E) has been identified, and is transcribed from 3 exons and 2 introns spanning 1.9kb as illustrated above. The difference occurs at the 5' untranslated region, but the two transcripts encode the same isoform. Mice do not have a gene orthologue to human ...

متن کامل

The Roles of CD137 Signaling in Atherosclerosis

The tumor necrosis factor receptor superfamily (TNFRSF), which includes CD40, LIGHT, and OX40, plays important roles in the initiation and progression of cardiovascular diseases, involving atherosclerosis. CD137, a member of TNFRSF, is a well-known activation-induced T cell co-stimulatory molecule and has been reported to be expressed in human atherosclerotic plaque lesions, and plays pivotal r...

متن کامل

Tumor necrosis factor superfamily in innate immunity and inflammation.

The tumor necrosis factor superfamily (TNFSF) and its corresponding receptor superfamily (TNFRSF) form communication pathways required for developmental, homeostatic, and stimulus-responsive processes in vivo. Although this receptor-ligand system operates between many different cell types and organ systems, many of these proteins play specific roles in immune system function. The TNFSF and TNFR...

متن کامل

Targeting inhibitor of apoptosis proteins to block vascular inflammation.

The tumor necrosis factor (TNF) receptor superfamily (TNFRSF) represents a large number of membranebound and secreted proteins that regulate inflammation and other functions in the vasculature and other tissues. Members of the TNFRSF are involved in the pathogenesis of atherosclerosis,1 and treatment with anti-TNF antibodies enhances vascular function in patients with arthritis.2 Activation of ...

متن کامل

Dual Philosophy in Death Receptor Signalling

Tumour necrosis factor (TNF) is the founding member of a cytokine family with important roles in both, physiology and pathological conditions. The two seemingly opposing cellular responses to stimulation by TNF itself are death and induction of pro-inflammatory signalling. TNF and other TNF superfamily (SF) members signal by crosslinking their cognate receptors. These form part of the TNF recep...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2011