Biology subjects

Herrero, A.

Publications and source records attributed to Herrero, A..

7 recordsLinked to original sources

bioRxiv2026

Circulating Immune Profiling Reveals Immune Signatures Associated with Disease Stage and Outcome in Endometrial Cancer

Although the tumor immune microenvironment has been studied in endometrial cancer, the systemic immune alterations associated with disease progression and their potential prognostic significance remain poorly defined. In this study, peripheral blood immune subsets were characterized by multiparametric flow cytometry in 67 patients with EC and 20 healthy controls, including dendritic cells, MDSCs, T-cell subsets, NK cells, and exhaustion and senescence associated markers. Immune profiles were similar between healthy controls and patients with early-stage disease, whereas advanced tumors showed marked changes, including dendritic cell expansion, reduced CD4+ T-cell proportions, and increased frequencies of CD8+CD27-CD28- and CD8+CD57+ populations. Among clinicopathologic features, MDSC levels were associated with tumor grade and myometrial infiltration, while regulatory T cells were increased in TP53-mutated and microsatellite-stable tumors. In the advanced cohort (n=31), non-responders frequently displayed elevated CD8+, CD8+CD27-CD28-, and CD8+CD57+ levels alongside decreased CD27+CD28+ proportions. In multivariable Cox models, higher baseline CD8+ (HR 1.13), CD8+ CD27-CD28- (HR 1.04), and CD8+CD57+ proportions (HR 1.07; all p<0.05) were independently associated with shorter PFS, whereas higher CD27+CD28+ levels were associated with improved PFS. CD27-CD28- proportions were also linked to worse PFS by Kaplan-Meier analysis (HR 5.1, log-rank p=0.005). Longitudinal analysis (n=28) showed that senescent-like lymphocyte levels remained associated with progression across timepoints (OR 18.80), whereas total CD8+ proportions diverged progressively, reaching significance only from 6 months onward. Together, these findings identify systemic immune remodeling as a characteristic of advanced endometrial cancer and support the potential of circulating immune profiling for patient stratification and prognostic assessment, pending validation in larger prospective cohorts.

cancer biology↗

bioRxiv2024

The role of the LysR-type transcription factor PacR in regulating nitrogen metabolism in Anabaena sp. PCC7120

In the filamentous model cyanobacterium Anabaena sp. PCC 7120 heterocyst formation is triggered by changes in the C/N-ratio and relies on transcriptional reprogramming in cells. The transcription factor PacR is thought to serve as a global regulator of carbon assimilation under photoautotrophic conditions. In response to Ci-availability, PacR may modulate the carbon concentrating mechanism and photosynthesis, balancing reducing power generation while protecting the photosynthetic apparatus from oxidative damage. However, PacR also binds to promoters of genes associated with heterocyst formation, although the underlying mechanisms remain unclear. To explore this, we studied a response of a PacR-deletion mutant to a nitrogen source shift from ammonium to nitrate. The absence of PacR led to the heterocyst formation in nitrate containing media, as well as reduced growth and chlorophyll-content. We observed impaired nitrate uptake and disrupted ammonium assimilation via the GOGAT-cycle. This phenotype may be exacerbated by reduced PSI-yield and reduced expression of ferredoxin, which may lead to less reducing equivalents for nitrogen assimilation. Our results provide insights into the regulation of heterocyst-formation in Anabaena, potentially advancing its use in biotechnological applications that utilize heterocyst as microoxic cell factories for N2-fixation and hydrogen production.

plant biology↗

bioRxiv2024

β-Glucan Reprograms Neutrophils to Induce Disease Tolerance Against Influenza A Virus

ABSTRACTDisease tolerance is an evolutionarily conserved host defence strategy that preserves tissue integrity and physiology without affecting pathogen load. Unlike host resistance, the mechanisms underlying disease tolerance remain poorly understood. In the present study, we investigated whether an adjuvant ({beta}-glucan) can reprogram innate immunity to provide protection against Influenza A virus (IAV) infection. Here we observe that {beta}-glucan treatment reduced the morbidity and mortality against IAV infection, independent of host resistance (viral load). Increased survival of {beta}-glucan treated mice against IAV is associated with the accumulation of neutrophils via RoR{gamma}t+ T cells in the lung tissue. Using gain-and-loss-of-function approaches, we demonstrate that {beta}- glucan reprogrammed neutrophils are essential for promoting disease tolerance, limiting pulmonary tissue damage, and enhancing survival against IAV infection. {beta}-glucan treatment promotes granulopoiesis in a type 1 interferon-dependent manner that leads to the generation of a unique subset of neutrophils, which are less mature with higher mitochondrial mass utilizing mitochondrial oxidative (OXPHOS) metabolism. Collectively, our data indicate that {beta}-glucan reprograms hematopoietic stem cells (HSCs) to generate neutrophils with a novel "regulatory" function, which is required for promoting disease tolerance and maintaining lung tissue integrity against viral infection.

immunology↗

bioRxiv2023

Growth sensitivity to water availability as potential indicator of drought-induced tree mortality in Mediterranean Pinus sylvestris forests

Drought-associated tree mortality has worldwide increased in the last decades, impacting structure and functioning of forest ecosystems, with implications for energy, carbon and water fluxes. However, the understanding of the factors underlying this mortality are still limited, especially at stand scale. We aim to identify the factors that triggered the mortality of the widely distributed Pinus sylvestris in an extensive forest area in central Spain. We compared radial growth patterns in pairs of live and recently dead individuals that co-occur in close proximity and present similar age and size, thereby isolating the effects of size and environment from the mortality process. Temporal dynamics of growth, growth synchrony, and growth sensitivity to water availability (P-PET) were compared between live and recently dead trees. Over the last 50 years, we observed an increase in the growth synchrony and sensitivity to water availability as drought conditions intensified consistent to prior research. However, no differences were found in radial growth between live and dead individuals 15 years before mortality, and dead individuals showed lower growth synchrony and sensitivity to water availability than live ones for much of the period studied. This suggests a decoupling between trees growth responses and climatic conditions, which could increase vulnerability to hydraulic failure and/or carbon starvation. Overall, our results point to an important role of growth sensitivity to water availability in tree mortality for P. sylvestris at its southern distribution limit.

ecology↗

bioRxiv2023

Forest structural diversity determines tree growth synchrony in response to climate change

After centuries of deforestation, many industrialised countries are experiencing an increase in forest area and biomass due to changes in land- and forest-use since the mid-20th century. At the same time, the impacts of climate change on forests are aggravating, but the interplay between past land- and forest-use (i.e. land- and forest-use legacies) and climate change in forest functioning remains elusive. Here using network theory and linear mixed models, we quantified how land- and forest-use legacies modulate tree growth synchrony in response to climate change. We analysed tree growth data from European beech (Fagus sylvatica L.) stands with different histories of forest management at the species rear edge. We found that tree growth synchrony increased following heatwaves, late spring frosts, and reduced precipitation. Interestingly, the greatest tree growth synchrony occurred in recently-established forests, while stands containing large trees and heterogeneous tree sizes showed much lower growth synchrony. Our results highlight the importance of maintaining large trees and structurally heterogeneous forests to mitigate the negative effects of climate change on forest productivity, and thereby, increase forest resilience to future forest climate risks.

ecology↗

bioRxiv2023

Spatio-temporal coherence of circadian clocks and gating of differentiation in Anabaena filaments

Circadian clock arrays in multicellular filaments of the heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120 display remarkable spatio-temporal coherence under nitrogen-replete conditions. To shed light on the interplay between circadian clocks and the formation of developmental patterns, we followed the expression of a clock-controlled gene under nitrogen deprivation, at the level of individual cells. Our experiments showed that differentiation into heterocysts took place preferentially within a limited interval of the circadian clock cycle; that gene expression in different vegetative intervals along a developed filament was discoordinated; and that the circadian clock was active in individual heterocysts. Furthermore, Anabaena mutants lacking the kaiABC genes encoding the circadian clock core components produced heterocysts but failed in diazotrophy. Therefore, genes related to some aspect of nitrogen fixation, rather than early or mid-heterocyst differentiation genes, are likely affected by the absence of the clock. A bioinformatics analysis supports the notion that RpaA may play a role as master regulator of clock outputs in Anabaena, the gating of differentiation by the circadian clock and the involvement of the clock in proper diazotrophic growth. Together, these results suggest that under nitrogen deficient conditions, the functional unit in Anabaena is reduced from a full filament under nitrogen-rich conditions, to the vegetative cell interval between heterocysts.

biophysics↗

bioRxiv2021

Characterisation of a nucleo-adhesome

In addition to central functions in cell adhesion signalling, integrin-associated proteins have wider roles at sites distal to adhesion receptors. In experimentally defined adhesomes, we noticed that there is clear enrichment of proteins that localise to the nucleus, and conversely, we now report that nuclear proteomes contain a class of adhesome components that localise to the nucleus. We here defined a nucleo-adhesome, providing experimental evidence for a remarkable scale of nuclear localisation of adhesion proteins, establishing a framework for interrogating nuclear adhesion protein functions. In adding to nuclear FAKs known roles in regulating transcription, we now show that nuclear FAK regulates expression of many adhesion-related proteins that localise to the nucleus and that nuclear FAK binds to the adhesome component and nuclear protein Hic-5. FAK and Hic-C work together in the nucleus, co-regulating a subset of genes transcriptionally. We describe the first nucleo-adhesome using a squamous cancer cell model, and demonstrate the new principle that there are nuclear adhesion protein subcomplexes that cooperate to control transcription. O_FIG O_LINKSMALLFIG WIDTH=177 HEIGHT=200 SRC="FIGDIR/small/458428v1_ufig1.gif" ALT="Figure 1"> View larger version (37K): org.highwire.dtl.DTLVardef@1c841ceorg.highwire.dtl.DTLVardef@586a75org.highwire.dtl.DTLVardef@b54439org.highwire.dtl.DTLVardef@921537_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗