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排序方式: 共有108条查询结果,搜索用时 62 毫秒
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Interleukin 21 and its receptor are involved in NK cell expansion and regulation of lymphocyte function 总被引:64,自引:0,他引:64
Parrish-Novak J Dillon SR Nelson A Hammond A Sprecher C Gross JA Johnston J Madden K Xu W West J Schrader S Burkhead S Heipel M Brandt C Kuijper JL Kramer J Conklin D Presnell SR Berry J Shiota F Bort S Hambly K Mudri S Clegg C Moore M Grant FJ Lofton-Day C Gilbert T Rayond F Ching A Yao L Smith D Webster P Whitmore T Maurer M Kaushansky K Holly RD Foster D 《Nature》2000,408(6808):57-63
Cytokines are important in the regulation of haematopoiesis and immune responses, and can influence lymphocyte development. Here we have identified a class I cytokine receptor that is selectively expressed in lymphoid tissues and is capable of signal transduction. The full-length receptor was expressed in BaF3 cells, which created a functional assay for ligand detection and cloning. Conditioned media from activated human CD3+ T cells supported proliferation of the assay cell line. We constructed a complementary DNA expression library from activated human CD3+ T cells, and identified a cytokine with a four-helix-bundle structure using functional cloning. This cytokine is most closely related to IL2 and IL15, and has been designated IL21 with the receptor designated IL21 R. In vitro assays suggest that IL21 has a role in the proliferation and maturation of natural killer (NK) cell populations from bone marrow, in the proliferation of mature B-cell populations co-stimulated with anti-CD40, and in the proliferation of T cells co-stimulated with anti-CD3. 相似文献
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McNew JA Parlati F Fukuda R Johnston RJ Paz K Paumet F Söllner TH Rothman JE 《Nature》2000,407(6801):153-159
Membrane-enveloped vesicles travel among the compartments of the cytoplasm of eukaryotic cells, delivering their specific cargo to programmed locations by membrane fusion. The pairing of vesicle v-SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein receptors) with target membrane t-SNAREs has a central role in intracellular membrane fusion. We have tested all of the potential v-SNAREs encoded in the yeast genome for their capacity to trigger fusion by partnering with t-SNAREs that mark the Golgi, the vacuole and the plasma membrane. Here we find that, to a marked degree, the pattern of membrane flow in the cell is encoded and recapitulated by its isolated SNARE proteins, as predicted by the SNARE hypothesis. 相似文献
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Sloan JL Johnston JJ Manoli I Chandler RJ Krause C Carrillo-Carrasco N Chandrasekaran SD Sysol JR O'Brien K Hauser NS Sapp JC Dorward HM Huizing M;NIH Intramural Sequencing Center Group Barshop BA Berry SA James PM Champaigne NL de Lonlay P Valayannopoulos V Geschwind MD Gavrilov DK Nyhan WL Biesecker LG Venditti CP 《Nature genetics》2011,43(9):883-886
We used exome sequencing to identify the genetic basis of combined malonic and methylmalonic aciduria (CMAMMA). We sequenced the exome of an individual with CMAMMA and followed up with sequencing of eight additional affected individuals (cases). This included one individual who was identified and diagnosed by searching an exome database. We identify mutations in ACSF3, encoding a putative methylmalonyl-CoA and malonyl-CoA synthetase as a cause of CMAMMA. We also examined a canine model of CMAMMA, which showed pathogenic mutations in a predicted ACSF3 ortholog. ACSF3 mutant alleles occur with a minor allele frequency of 0.0058 in ~1,000 control individuals, predicting a CMAMMA population incidence of ~1:30,000. ACSF3 deficiency is the first human disorder identified as caused by mutations in a gene encoding a member of the acyl-CoA synthetase family, a diverse group of evolutionarily conserved proteins, and may emerge as one of the more common human metabolic disorders. 相似文献
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Stephanie Duguez William Duddy Helen Johnston Jeanne Lainé Marie Catherine Le Bihan Kristy J. Brown Anne Bigot Yetrib Hathout Gillian Butler-Browne Terence Partridge 《Cellular and molecular life sciences : CMLS》2013,70(12):2159-2174
Duchenne muscular dystrophy results from loss of the protein dystrophin, which links the intracellular cytoskeletal network with the extracellular matrix, but deficiency in this function does not fully explain the onset or progression of the disease. While some intracellular events involved in the degeneration of dystrophin-deficient muscle fibers have been well characterized, changes in their secretory profile are undescribed. To analyze the secretome profile of mdx myotubes independently of myonecrosis, we labeled the proteins of mdx and wild-type myotubes with stable isotope-labeled amino acids (SILAC), finding marked enrichment of vesicular markers in the mdx secretome. These included the lysosomal-associated membrane protein, LAMP1, that co-localized in vesicles with an over-secreted cytoskeletal protein, myosin light chain 1. These LAMP1/MLC1-3-positive vesicles accumulated in the cytosol of mdx myotubes and were secreted into the culture medium in a range of abnormal densities. Restitution of dystrophin expression, by exon skipping, to some 30 % of the control value, partially normalized the secretome profile and the excess LAMP1 accumulation. Together, our results suggest that a lack of dystrophin leads to a general dysregulation of vesicle trafficking. We hypothesize that disturbance of the export of proteins through vesicles occurs before, and then concurrently with, the myonecrotic cascade and contributes chronically to the pathophysiology of DMD, thereby presenting us with a range of new potential therapeutic targets. 相似文献
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Adrenergic receptors were first classified into two calsses--alpha and beta--on the basis of the relative pharmacological potencies of agonist compounds, and this classification has been supported by subsequent studies. In some tissues, such as the heart and liver, they exert similar physiological responses, and in other tissues, such as the uterus and vasculature, they have opposing roles. The occurrence of both classes of receptor in the same tissue lewwds to the problem of what determines whether the overall response observed is alpha-type or beta-type, as adrenaline and noradrenaline bind to both receptor classes. Furthermore, direct binding studies have demonstrated that the two receptor classes are distinct and separate entities. We show here that stimulation of alpha-receptors in renal membranes causes a specific decrease in the affinity of the agonist compound isoprenaline for beta-receptors in the same membranes. This demonstrates that interactions occur between renal alpha- and beta-adrenergic receptors. Such interactions may modulate the response of the kidney to sympathetic stimulation. 相似文献