54 research outputs found
Host-Based Th2 Cell Therapy for Prolongation of Cardiac Allograft Viability
Donor T cell transfusion, which is a long-standing approach to prevent allograft rejection, operates indirectly by alteration of host T cell immunity. We therefore hypothesized that adoptive transfer of immune regulatory host Th2 cells would represent a novel intervention to enhance cardiac allograft survival. Using a well-described rat cardiac transplant model, we first developed a method for ex vivo manufacture of rat host-type Th2 cells in rapamycin, with subsequent injection of such Th2.R cells prior to class I and class II disparate cardiac allografting. Second, we determined whether Th2.R cell transfer polarized host immunity towards a Th2 phenotype. And third, we evaluated whether Th2.R cell therapy prolonged allograft viability when used alone or in combination with a short-course of cyclosporine (CSA) therapy. We found that host-type Th2.R cell therapy prior to cardiac allografting: (1) reduced the frequency of activated T cells in secondary lymphoid organs; (2) shifted post-transplant cytokines towards a Th2 phenotype; and (3) prolonged allograft viability when used in combination with short-course CSA therapy. These results provide further support for the rationale to use “direct” host T cell therapy for prolongation of allograft viability as an alternative to “indirect” therapy mediated by donor T cell infusion
Distinct Roles of Non-Canonical Poly(A) Polymerases in RNA Metabolism
Trf4p and Trf5p are non-canonical poly(A) polymerases and are part of the heteromeric protein complexes TRAMP4 and TRAMP5 that promote the degradation of aberrant and short-lived RNA substrates by interacting with the nuclear exosome. To assess the level of functional redundancy between the paralogous Trf4 and Trf5 proteins and to investigate the role of the Trf4-dependent polyadenylation in vivo, we used DNA microarrays to compare gene expression of the wild-type yeast strain of S. cerevisiae with either that of trf4Δ or trf5Δ mutant strains or the trf4Δ mutant expressing the polyadenylation-defective Trf4(DADA) protein. We found little overlap between the sets of transcripts with altered expression in the trf4Δ or the trf5Δ mutants, suggesting that Trf4p and Trf5p target distinct groups of RNAs for degradation. Surprisingly, most RNAs the expression of which was altered by the trf4 deletion were restored to wild-type levels by overexpression of TRF4(DADA), showing that the polyadenylation activity of Trf4p is dispensable in vivo. Apart from previously reported Trf4p and Trf5p target RNAs, this analysis along with in vivo cross-linking and RNA immunopurification-chip experiments revealed that both the TRAMP4 and the TRAMP5 complexes stimulate the degradation of spliced-out introns via a mechanism that is independent of the polyadenylation activity of Trf4p. In addition, we show that disruption of trf4 causes severe shortening of telomeres suggesting that TRF4 functions in the maintenance of telomere length. Finally, our study demonstrates that TRF4, the exosome, and TRF5 participate in antisense RNA–mediated regulation of genes involved in phosphate metabolism. In conclusion, our results suggest that paralogous TRAMP complexes have distinct RNA selectivities with functional implications in RNA surveillance as well as other RNA–related processes. This indicates widespread and integrative functions of TRAMP complexes for the coordination of different gene expression regulatory processes
Fat Oxidation, Fitness and Skeletal Muscle Expression of Oxidative/Lipid Metabolism Genes in South Asians: Implications for Insulin Resistance?
<p><b>Background:</b> South Asians are more insulin resistant than Europeans, which cannot be fully explained by differences in adiposity. We investigated whether differences in oxidative capacity and capacity for fatty acid utilisation in South Asians might contribute, using a range of whole-body and skeletal muscle measures.</p>
<p><b>Methodology/Principal Findings:</b> Twenty men of South Asian ethnic origin and 20 age and BMI-matched men of white European descent underwent exercise and metabolic testing and provided a muscle biopsy to determine expression of oxidative and lipid metabolism genes and of insulin signalling proteins. In analyses adjusted for age, BMI, fat mass and physical activity, South Asians, compared to Europeans, exhibited; reduced insulin sensitivity by 26% (p = 0.010); lower VO2max (40.6±6.6 vs 52.4±5.7 ml.kg−1.min−1, p = 0.001); and reduced fat oxidation during submaximal exercise at the same relative (3.77±2.02 vs 6.55±2.60 mg.kg−1.min−1 at 55% VO2max, p = 0.013), and absolute (3.46±2.20 vs 6.00±1.93 mg.kg−1.min−1 at 25 ml O2.kg−1.min−1, p = 0.021), exercise intensities. South Asians exhibited significantly higher skeletal muscle gene expression of CPT1A and FASN and significantly lower skeletal muscle protein expression of PI3K and PKB Ser473 phosphorylation. Fat oxidation during submaximal exercise and VO2max both correlated significantly with insulin sensitivity index and PKB Ser473 phosphorylation, with VO2max or fat oxidation during exercise explaining 10–13% of the variance in insulin sensitivity index, independent of age, body composition and physical activity.</p>
<p><b>Conclusions/Significance:</b> These data indicate that reduced oxidative capacity and capacity for fatty acid utilisation at the whole body level are key features of the insulin resistant phenotype observed in South Asians, but that this is not the consequence of reduced skeletal muscle expression of oxidative and lipid metabolism genes.</p>
The Staphylococcus aureus Response to Unsaturated Long Chain Free Fatty Acids: Survival Mechanisms and Virulence Implications
Staphylococcus aureus is an important human commensal and opportunistic pathogen responsible for a wide range of infections. Long chain unsaturated free fatty acids represent a barrier to colonisation and infection by S. aureus and act as an antimicrobial component of the innate immune system where they are found on epithelial surfaces and in abscesses. Despite many contradictory reports, the precise anti-staphylococcal mode of action of free fatty acids remains undetermined. In this study, transcriptional (microarrays and qRT-PCR) and translational (proteomics) analyses were applied to ascertain the response of S. aureus to a range of free fatty acids. An increase in expression of the σB and CtsR stress response regulons was observed. This included increased expression of genes associated with staphyloxanthin synthesis, which has been linked to membrane stabilisation. Similarly, up-regulation of genes involved in capsule formation was recorded as were significant changes in the expression of genes associated with peptidoglycan synthesis and regulation. Overall, alterations were recorded predominantly in pathways involved in cellular energetics. In addition, sensitivity to linoleic acid of a range of defined (sigB, arcA, sasF, sarA, agr, crtM) and transposon-derived mutants (vraE, SAR2632) was determined. Taken together, these data indicate a common mode of action for long chain unsaturated fatty acids that involves disruption of the cell membrane, leading to interference with energy production within the bacterial cell. Contrary to data reported for other strains, the clinically important EMRSA-16 strain MRSA252 used in this study showed an increase in expression of the important virulence regulator RNAIII following all of the treatment conditions tested. An adaptive response by S. aureus of reducing cell surface hydrophobicity was also observed. Two fatty acid sensitive mutants created during this study were also shown to diplay altered pathogenesis as assessed by a murine arthritis model. Differences in the prevalence and clinical importance of S. aureus strains might partly be explained by their responses to antimicrobial fatty acids
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions
Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9orf72) have recently been linked to frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis, and may be the most common genetic cause of both neurodegenerative diseases. Genetic variants at TMEM106B influence risk for the most common neuropathological subtype of FTLD, characterized by inclusions of TAR DNA-binding protein of 43 kDa (FTLD-TDP). Previous reports have shown that TMEM106B is a genetic modifier of FTLD-TDP caused by progranulin (GRN) mutations, with the major (risk) allele of rs1990622 associating with earlier age at onset of disease. Here, we report that rs1990622 genotype affects age at death in a single-site discovery cohort of FTLD patients with C9orf72 expansions (n = 14), with the major allele correlated with later age at death (p = 0.024). We replicate this modifier effect in a 30-site international neuropathological cohort of FTLD-TDP patients with C9orf72 expansions (n = 75), again finding that the major allele associates with later age at death (p = 0.016), as well as later age at onset (p = 0.019). In contrast, TMEM106B genotype does not affect age at onset or death in 241 FTLD-TDP cases negative for GRN mutations or C9orf72 expansions. Thus, TMEM106B is a genetic modifier of FTLD with C9orf72 expansions. Intriguingly, the genotype that confers increased risk for developing FTLD-TDP (major, or T, allele of rs1990622) is associated with later age at onset and death in C9orf72 expansion carriers, providing an example of sign epistasis in human neurodegenerative disease
Spatial ecology of a small desert shrub on adjacent geological substrates
1. Spatial pattern analyses were used to generate hypotheses about the processes that shape the structure of a plant community in the Mojave Desert of North America, with a focus on the semi-shrub Ambrosia dumosa. We analysed spatial distributions and sizes of this species relative to other semi-shrubs, shrubs and annuals, and the relationships between spatial patterns and abiotic and biotic habitat characteristics. 2. The analyses were based on maps of sample plots placed along a transect spanning two adjacent geological substrates: aeolian sand and gravelly, sandy to loamy alluvium. Of these two substrates, sand supported higher total biomasses of Ambrosia and of all woody perennials, while alluvium supported on average higher biomasses of winter annuals. 3. Annuals and seedlings of Ambrosia were much more strongly aggregated with Ambrosia canopies on sand than on alluvium, suggesting that these small plants were more strongly facilitated by Ambrosia on sand than on alluvium. 4. Ambrosia semi-shrubs were spatially segregated on sand but aggregated on alluvium, and the degree of segregation on sand increased with the total above-ground biomass of Ambrosia per unit area, indicating that negative interactions between Ambrosia plants were stronger in more productive habitats. Canopy sizes of Ambrosia in all mapped plots increased with distance to the nearest conspecific neighbour, which suggests that neighbour interactions negatively affected plant sizes. 5. Ambrosia plants on sand were spatially aggregated with Acamptopappus sphaerocephalus semi-shrubs, suggesting that at least one of these species may benefit from the association. Ambrosia plants were spatially segregated from Larrea tridentata shrubs on both substrates, possibly due to negative effects of Larrea roots on Ambrosia roots reported in previous studies. 6. Subtle differences in substrate characteristics were correlated with strong differences in the spatial distribution of Ambrosia plants relative to their neighbours, which suggests that edaphic conditions may affect the spatial structure of the community by modifying complex positive and negative interactions between neighbouring plants
Spatial ecology of a small desert shrub on adjacent geological substrates
Summary 1 Spatial pattern analyses were used to generate hypotheses about the processes that shape the structure of a plant community in the Mojave Desert of North America, with a focus on the semi-shrub Ambrosia dumosa . We analysed spatial distributions and sizes of this species relative to other semi-shrubs, shrubs and annuals, and the relationships between spatial patterns and abiotic and biotic habitat characteristics. 2 The analyses were based on maps of sample plots placed along a transect spanning two adjacent geological substrates: aeolian sand and gravelly, sandy to loamy alluvium. Of these two substrates, sand supported higher total biomasses of Ambrosia and of all woody perennials, while alluvium supported on average higher biomasses of winter annuals. 3 Annuals and seedlings of Ambrosia were much more strongly aggregated with Ambrosia canopies on sand than on alluvium, suggesting that these small plants were more strongly facilitated by Ambrosia on sand than on alluvium. 4 Ambrosia semi-shrubs were spatially segregated on sand but aggregated on alluvium, and the degree of segregation on sand increased with the total above-ground biomass of Ambrosia per unit area, indicating that negative interactions between Ambrosia plants were stronger in more productive habitats. Canopy sizes of Ambrosia in all mapped plots increased with distance to the nearest conspecific neighbour, which suggests that neighbour interactions negatively affected plant sizes. 5 Ambrosia plants on sand were spatially aggregated with Acamptopappus sphaerocephalus semi-shrubs, suggesting that at least one of these species may benefit from the association. Ambrosia plants were spatially segregated from Larrea tridentata shrubs on both substrates, possibly due to negative effects of Larrea roots on Ambrosia roots reported in previous studies. 6 Subtle differences in substrate characteristics were correlated with strong differences in the spatial distribution of Ambrosia plants relative to their neighbours, which suggests that edaphic conditions may affect the spatial structure of the community by modifying complex positive and negative interactions between neighbouring plants
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