85 research outputs found
EL SILENCIO EN EL MONSTRUO DEL MANZANARES
Este trabajo estudia la funciĂłn del silencio en la novela El monstruo del
Manzanares, novela corta incluida en la colección La mojiganga del gusto (1641) de Andrés
Sanz del Castillo. Esta novela posee constantes alusiones al silencio, las cuales, sumadas a la
ausencia de diálogos que reproduzcan las voces de los personajes, nos llevan a considerar, más
allá todavĂa, que el silencio configura un tema en sĂ mismo dentro de El monstruo de Manzanares
y determina notoriamente el sentido final de la novela
Table1_HMGB1 is a mediator of cuproptosis-related sterile inflammation.XLSX
Cuproptosis is a recently recognized modality of cell death driven by intracellular copper-dependent mitochondrial stress. However, the mediators of the sterile inflammatory response to cuproptotic death are undetermined. Here, we report that high-mobility group box 1 (HMGB1), a damage-associated molecular pattern, is released by cuproptotic cells to initiate inflammation. Mechanically, copper accumulation-induced adenosine triphosphate (ATP) depletion activates AMP-activated protein kinase (AMPK) to promote HMGB1 phosphorylation, resulting in increased extracellular release. In contrast, genetic (using RNAi) or pharmacologic (using dorsomorphin) inhibition of AMPK activation limits cuproptosis and HMGB1 release. Functionally, the ability of HMGB1-deficient cuproptotic cells to promote advanced glycosylation end product-specific receptor (AGER, also known as RAGE)-dependent inflammatory cytokine production is greatly reduced. Thus, HMGB1 is a key immune mediator of cuproptosis-initiated sterile inflammation.</p
Table2_HMGB1 is a mediator of cuproptosis-related sterile inflammation.XLSX
Cuproptosis is a recently recognized modality of cell death driven by intracellular copper-dependent mitochondrial stress. However, the mediators of the sterile inflammatory response to cuproptotic death are undetermined. Here, we report that high-mobility group box 1 (HMGB1), a damage-associated molecular pattern, is released by cuproptotic cells to initiate inflammation. Mechanically, copper accumulation-induced adenosine triphosphate (ATP) depletion activates AMP-activated protein kinase (AMPK) to promote HMGB1 phosphorylation, resulting in increased extracellular release. In contrast, genetic (using RNAi) or pharmacologic (using dorsomorphin) inhibition of AMPK activation limits cuproptosis and HMGB1 release. Functionally, the ability of HMGB1-deficient cuproptotic cells to promote advanced glycosylation end product-specific receptor (AGER, also known as RAGE)-dependent inflammatory cytokine production is greatly reduced. Thus, HMGB1 is a key immune mediator of cuproptosis-initiated sterile inflammation.</p
DataSheet1_HMGB1 is a mediator of cuproptosis-related sterile inflammation.PDF
Cuproptosis is a recently recognized modality of cell death driven by intracellular copper-dependent mitochondrial stress. However, the mediators of the sterile inflammatory response to cuproptotic death are undetermined. Here, we report that high-mobility group box 1 (HMGB1), a damage-associated molecular pattern, is released by cuproptotic cells to initiate inflammation. Mechanically, copper accumulation-induced adenosine triphosphate (ATP) depletion activates AMP-activated protein kinase (AMPK) to promote HMGB1 phosphorylation, resulting in increased extracellular release. In contrast, genetic (using RNAi) or pharmacologic (using dorsomorphin) inhibition of AMPK activation limits cuproptosis and HMGB1 release. Functionally, the ability of HMGB1-deficient cuproptotic cells to promote advanced glycosylation end product-specific receptor (AGER, also known as RAGE)-dependent inflammatory cytokine production is greatly reduced. Thus, HMGB1 is a key immune mediator of cuproptosis-initiated sterile inflammation.</p
Data_Sheet_1_Arbuscular mycorrhizal and ectomycorrhizal plants together shape seedling diversity in a subtropical forest.ZIP
IntroductionBurgeoning mycorrhizal research has focused on identifying the various diverse mycorrhizal strategies of forest communities. Mounting evidence suggests that mycorrhizae play important roles in regulating forest community structure and composition. However, research into the manifestation of this influence in the seedling stage is lacking, especially in small-scale plots.MethodsOur research utilized structural equation models parameterized using data from a subtropical monsoon broad-leaved evergreen forest situated in Yunnan Province, China.ResultsWe noted that seedlings included plants that utilized both arbuscular mycorrhizal (AM) and ectomycorrhizal (EM) fungi. More seedling plots with the relatively higher species diversity were the product of the mixed mycorrhizal strategy, meaning the coexistence of AM and EM seedlings in a small-scale plot rather than the dominance of one type of strategies. These mixed communities were primarily found on slopes and mountain ridges. The abundance of AM or EM trees indirectly affected seedling diversity by influencing the abundance of different mycorrhizal seedlings. In this case, the diversity of the mixed mycorrhizal community was also restricted by the level of leaf thickness in the community, followed by abiotic factors such as elevation, convexity, soil pH and soil available phosphorus.DiscussionThe effect of leaf thickness on mycorrhizal seedling abundance reflected the importance of water conditions in shaping seedling communities. The effect of convexity on seedling diversity also reflected the limitation of seedling communities by the distribution of humidity and heat conditions during topographic change. The results suggested that it is crucial to preserve seedling diversity via the mixed mycorrhizal strategy of communities in the subtropical forest.</p
Image_2_Arbuscular mycorrhizal and ectomycorrhizal plants together shape seedling diversity in a subtropical forest.TIFF
IntroductionBurgeoning mycorrhizal research has focused on identifying the various diverse mycorrhizal strategies of forest communities. Mounting evidence suggests that mycorrhizae play important roles in regulating forest community structure and composition. However, research into the manifestation of this influence in the seedling stage is lacking, especially in small-scale plots.MethodsOur research utilized structural equation models parameterized using data from a subtropical monsoon broad-leaved evergreen forest situated in Yunnan Province, China.ResultsWe noted that seedlings included plants that utilized both arbuscular mycorrhizal (AM) and ectomycorrhizal (EM) fungi. More seedling plots with the relatively higher species diversity were the product of the mixed mycorrhizal strategy, meaning the coexistence of AM and EM seedlings in a small-scale plot rather than the dominance of one type of strategies. These mixed communities were primarily found on slopes and mountain ridges. The abundance of AM or EM trees indirectly affected seedling diversity by influencing the abundance of different mycorrhizal seedlings. In this case, the diversity of the mixed mycorrhizal community was also restricted by the level of leaf thickness in the community, followed by abiotic factors such as elevation, convexity, soil pH and soil available phosphorus.DiscussionThe effect of leaf thickness on mycorrhizal seedling abundance reflected the importance of water conditions in shaping seedling communities. The effect of convexity on seedling diversity also reflected the limitation of seedling communities by the distribution of humidity and heat conditions during topographic change. The results suggested that it is crucial to preserve seedling diversity via the mixed mycorrhizal strategy of communities in the subtropical forest.</p
MiR-6835 promoted LPS-induced inflammation of HUVECs associated with the interaction between TLR-4 and AdipoR1 in lipid rafts
<div><p>Background</p><p>High mortality rate of critically-ill patients could be induced by sepsis and septic shock, which is the extremely life threatening. The purpose of this work is to identify and evaluate the potential regulatory mechanism of LPS-induced inflammation associated with miR-6835 and lipid rafts in HUVECs.</p><p>Methods</p><p>The 3’ UTR luciferase activity of AdipoR1 was detected, which was predicted the potential target gene of miR-6835. Moreover, the treated HUVECs with or without inhibitors or mimics of miR-6835 were used. Furthermore, the bio-functions of HUVECs were explored. The protein expression levels of SIRT-1, AMPK, and AdipoR1 were assessed, which were involved in the AdipoR1 signaling pathway. Then, the interaction between TLR-4 and AdipoR1 in lipid rafts and its mediation role on LPS-induced inflammation was investigated in HUVECs.</p><p>Results</p><p>MiR-6835 targeted directly on AdipoR1, and suppressed its expression in mRNA (mimics of miR-6835: 0.731±0.016 vs control: 1.527±0.015, <i>P</i><0.001) and proteins levels, then regulated protein expression of SIRT-1 and AMPK, which were the downstream target genes of AdipoR1 signaling pathway. MiR-6835 enhanced LPS-induced inflammation process in HUVECs (TNF-α: LPS+mimics of miR-6835: 1638.51±78.43 vs LPS: 918.73±39.73, <i>P</i><0.001; IL-6: LPS+mimics of miR-6835: 1249.35±69.51 vs LPS: 687.52±43.64, <i>P</i><0.001), which was associated with the interaction between TLR-4 and AdipoR1 in lipid rafts.</p><p>Conclusions</p><p>MiR-6835 is the key regulator of LPS-induced inflammation process in HUVECs. The interaction between TLR-4 and AdipoR1 mediated by lipid rafts at membrane of HUVECs with inflammation process induced by miR-6835. Our results demonstrated a hopeful strategy for treatment on sepsis by aiming at lipid rafts and miR-6835.</p></div
Image_1_Arbuscular mycorrhizal and ectomycorrhizal plants together shape seedling diversity in a subtropical forest.TIFF
IntroductionBurgeoning mycorrhizal research has focused on identifying the various diverse mycorrhizal strategies of forest communities. Mounting evidence suggests that mycorrhizae play important roles in regulating forest community structure and composition. However, research into the manifestation of this influence in the seedling stage is lacking, especially in small-scale plots.MethodsOur research utilized structural equation models parameterized using data from a subtropical monsoon broad-leaved evergreen forest situated in Yunnan Province, China.ResultsWe noted that seedlings included plants that utilized both arbuscular mycorrhizal (AM) and ectomycorrhizal (EM) fungi. More seedling plots with the relatively higher species diversity were the product of the mixed mycorrhizal strategy, meaning the coexistence of AM and EM seedlings in a small-scale plot rather than the dominance of one type of strategies. These mixed communities were primarily found on slopes and mountain ridges. The abundance of AM or EM trees indirectly affected seedling diversity by influencing the abundance of different mycorrhizal seedlings. In this case, the diversity of the mixed mycorrhizal community was also restricted by the level of leaf thickness in the community, followed by abiotic factors such as elevation, convexity, soil pH and soil available phosphorus.DiscussionThe effect of leaf thickness on mycorrhizal seedling abundance reflected the importance of water conditions in shaping seedling communities. The effect of convexity on seedling diversity also reflected the limitation of seedling communities by the distribution of humidity and heat conditions during topographic change. The results suggested that it is crucial to preserve seedling diversity via the mixed mycorrhizal strategy of communities in the subtropical forest.</p
MiR-6835 targeted at AdipoR1 in HUVECs.
<p>The results showed the obviously down-regulated 3’ UTR activities of AdipoR1 in HUVECs, but no alternations were found while AdipoR1 with mutation. Moreover, miR-6835 could not directly target at AMPK, SIRT-1, and TLR-4, respectively. The data are presented as means±SD from three independent experiments. *<i>P</i><0.05, **<i>P</i><0.01.</p
AdipoR1 could bond with TLR-4.
<p>(A) The results CO-IP’d (co-immunoprecipitated) assay was perfomed, and identified the interaction between AdipoR1 and TLR-4. (B) The confocal images demonstrated that both the two recombinant proteins of AdipoR1 and TLR-4 localized at cell membrane of HUVECs with overlaid exhibition.</p
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