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Full-Text Articles in Life Sciences
Maturation Requirements For Dendritic Cells In T Cell Stimulation Leading To Tolerance Versus Immunity, Helen O'Neill, Jonathan Tan
Maturation Requirements For Dendritic Cells In T Cell Stimulation Leading To Tolerance Versus Immunity, Helen O'Neill, Jonathan Tan
Jonathan Tan
The model that dendritic cell (DC) "maturation" describes the change from an immature, antigen-capturing cell to a mature, antigen-presenting cell is well-established. Classification of DCs in terms of function has been problematic previously. It is therefore proposed that mature and not immature DCs are responsible for antigen presentation and stimulation of T cells. Furthermore, DC antigen presentation to T cells can have two outcomes: tolerance or immunity. The particular outcomes appear to be determined by the activation state of the mature DC. DCs can be activated by a range of environmental stimuli or "danger signals". Here, the hypothesis is advanced …
The Caenorhabditis Elegans Heterochronic Regulator Lin-14 Is A Novel Transcription Factor That Controls The Developmental Timing Of Transcription From The Insulin/Insulin-Like Growth Factor Gene Ins-33 By Direct Dna Binding., Marta Hristova, Darcy Birse, Yang Hong, Victor R. Ambros
The Caenorhabditis Elegans Heterochronic Regulator Lin-14 Is A Novel Transcription Factor That Controls The Developmental Timing Of Transcription From The Insulin/Insulin-Like Growth Factor Gene Ins-33 By Direct Dna Binding., Marta Hristova, Darcy Birse, Yang Hong, Victor R. Ambros
Victor R. Ambros
A temporal gradient of the novel nuclear protein LIN-14 specifies the timing and sequence of stage-specific developmental events in Caenorhabditis elegans. The profound effects of lin-14 mutations on worm development suggest that LIN-14 directly or indirectly regulates stage-specific gene expression. We show that LIN-14 can associate with chromatin in vivo and has in vitro DNA binding activity. A bacterially expressed C-terminal domain of LIN-14 was used to select DNA sequences that contain a putative consensus binding site from a pool of randomized double-stranded oligonucleotides. To identify candidates for genes directly regulated by lin-14, we employed DNA microarray hybridization to compare …
Developmental Biology. Encountering Micrornas In Cell Fate Signaling., Xantha Karp, Victor Ambros
Developmental Biology. Encountering Micrornas In Cell Fate Signaling., Xantha Karp, Victor Ambros
Victor R. Ambros
Comment on: LIN-12/Notch activation leads to microRNA-mediated down-regulation of Vav in C. elegans. [Science. 2005]
Silencing Of Retrotransposons In Dictyostelium By Dna Methylation And Rnai., Markus Kuhlmann, Branimira E. Borisova, Markus Kaller, Pontus Larsson, Dirk Stach, Jianbo Na, Ludwig Eichinger, Frank Lyko, Victor R. Ambros, Fredrik Soderbom, Christian Hammann, Wolfgang Nellen
Silencing Of Retrotransposons In Dictyostelium By Dna Methylation And Rnai., Markus Kuhlmann, Branimira E. Borisova, Markus Kaller, Pontus Larsson, Dirk Stach, Jianbo Na, Ludwig Eichinger, Frank Lyko, Victor R. Ambros, Fredrik Soderbom, Christian Hammann, Wolfgang Nellen
Victor R. Ambros
We have identified a DNA methyltransferase of the Dnmt2 family in Dictyostelium that was denominated DnmA. Expression of the dnmA gene is downregulated during the developmental cycle. Overall DNA methylation in Dictyostelium is approximately 0.2% of the cytosine residues, which indicates its restriction to a limited set of genomic loci. Bisulfite sequencing of specific sites revealed that DnmA is responsible for methylation of mostly asymmetric C-residues in the retrotransposons DIRS-1 and Skipper. Disruption of the gene resulted in a loss of methylation and in increased transcription and mobilization of Skipper. Skipper transcription was also upregulated in strains that had genes …
Mesodermally Expressed Drosophila Microrna-1 Is Regulated By Twist And Is Required In Muscles During Larval Growth., Nicholas S. Sokol, Victor R. Ambros
Mesodermally Expressed Drosophila Microrna-1 Is Regulated By Twist And Is Required In Muscles During Larval Growth., Nicholas S. Sokol, Victor R. Ambros
Victor R. Ambros
Although hundreds of evolutionarily conserved microRNAs have been discovered, the functions of most remain unknown. Here, we describe the embryonic spatiotemporal expression profile, transcriptional regulation, and loss-of-function phenotype of Drosophila miR-1 (DmiR-1). DmiR-1 RNA is highly expressed throughout the mesoderm of early embryos and subsequently in somatic, visceral, and pharyngeal muscles, and the dorsal vessel. The expression of DmiR-1 is controlled by the Twist and Mef2 transcription factors. DmiR-1KO mutants, generated using ends-in gene targeting, die as small, immobilized second instar larvae with severely deformed musculature. This lethality is rescued when a DmiR-1 transgene is expressed specifically in the mesoderm …
Graduate Colloquium, Borbala Mazzag
The Immunogenicity Of Dendritic Cell-Derived Exosomes, Ben Quah, Helen O'Neill
The Immunogenicity Of Dendritic Cell-Derived Exosomes, Ben Quah, Helen O'Neill
Helen O'Neill
Exosome production represents an alternate endocytic pathway for secretion. Multivesicular endosomes (MVE) fuse with the plasma membrane expelling internal vesicles or exosomes from cells. Exosome production has been recently described for immune cells including B cells, dendritic cells (DC), mast cells, macrophages and T cells. Exosomes derived from some DC populations stimulate T lymphocyte proliferation in vitro and have potent capacity to generate anti-tumour immune responses in vivo. These reported studies have involved in vitro grown mature DC expanded from precursors with cytokines. However, immature DC produce higher numbers of exosomes than mature DC and this is thought to be …
Maturation Requirements For Dendritic Cells In T Cell Stimulation Leading To Tolerance Versus Immunity, Helen O'Neill, Jonathan Tan
Maturation Requirements For Dendritic Cells In T Cell Stimulation Leading To Tolerance Versus Immunity, Helen O'Neill, Jonathan Tan
Helen O'Neill
The model that dendritic cell (DC) "maturation" describes the change from an immature, antigen-capturing cell to a mature, antigen-presenting cell is well-established. Classification of DCs in terms of function has been problematic previously. It is therefore proposed that mature and not immature DCs are responsible for antigen presentation and stimulation of T cells. Furthermore, DC antigen presentation to T cells can have two outcomes: tolerance or immunity. The particular outcomes appear to be determined by the activation state of the mature DC. DCs can be activated by a range of environmental stimuli or "danger signals". Here, the hypothesis is advanced …