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Miralles, F.

Publications and source records attributed to Miralles, F..

4 recordsLinked to original sources

Topological dependent modifications of gene expression in the preeclamptic placenta under aspirin treatment.

Preeclampsia is a hypertensive disorder of pregnancy characterized by systemic endothelial dysfunction and placental inflammatory activation. Low dose aspirin reduces preeclampsia incidence when initiated early, yet its molecular effects on the diseased human placenta remain poorly defined. We performed a topologically resolved transcriptomic analysis of placentas from two independent cohorts of preeclamptic women treated or not with aspirin. Placental samples were obtained either from the villous surface (syncytiotrophoblast rich) or from deep parenchymal regions (stromal and endothelial rich). In villous samples, microarray profiling identified 1,836 differentially expressed genes, predominantly down regulated. Gene set enrichment demonstrated marked suppression of pathways central to hypertensive placental pathology, including TNF/NF {kappa}B signaling, hypoxia responsive programs, glycolysis, and estrogen response cascades. RNA seq analysis of parenchymal samples identified 645 differentially expressed genes, again dominated by down regulation of cell cycle progression, mTORC1 signaling, inflammatory pathways, and metabolic stress responses. Across cohorts, 116 genes were consistently down regulated by aspirin and enriched for hypoxia, NF {kappa}B, estrogen response, and inflammatory signatures. Promoter analysis implicated transcription factors central to vascular inflammation and stress signaling, including NF {kappa}B1, RELA, HIF1A, PPARG, and PARP1. Functional validation in BeWo trophoblasts confirmed aspirin dependent modulation of key placental transcripts and altered secretion of MMP9, ANGPT2, and soluble endoglin (sENG) molecules directly implicated in endothelial dysfunction and hypertensive disease. These findings demonstrate that aspirin attenuates core inflammatory, hypoxic, and metabolic pathways across multiple placental lineages in preeclampsia, providing a mechanistic framework linking early aspirin administration to improved vascular and placental adaptation in hypertensive pregnancy. The action of aspirin upon differentiation of trophoblasts contribute to explain why aspirin protects only when administered early in pregnancy, before the end of the first trimester.

molecular biology↗

Decoding the pituitary gonadotrope regulatory architecture governing the preovulatory surge in vivo

Despite the global burden of female infertility, the molecular control of ovulation remains unclear. Pituitary gonadotropes tune hormonal output to regulate ovarian function, yet the molecular mechanisms that control their function during the sexual cycle remain poorly understood. Using state-of-the-art single-nucleus multiomic profiling of the female rat pituitary across the estrus cycle, we uncover unexpected cyclic epigenetic and transcriptional remodelling in gonadotrope cells, particularly during the preovulatory surge. This plasticity is driven by a biphasic gene regulatory network switch that orchestrates large-scale reorganisation of the secretory machinery. We further demonstrate that, contrary to the prevailing model, the LH surge does not depend on Lhb transcriptional upregulation. Instead, the FSH surge arises from dynamic Fshb transcription mediated by a complex combination of newly identified enhancers and key transcription factors. Overall, our findings define a new molecular framework for gonadotropin surge regulation and provide a foundational resource for understanding female reproductive disorders.

physiology↗

Radiolabeling Isolated Mitochondria with Tc-99m: A First-in-Field Protocol and Early Feasibility Findings

Mitochondrial transplantation is a promising but still experimental strategy for treating ischemic and metabolic disorders. A key barrier to its advancement is the lack of scalable, non-invasive methods for tracking transplanted extracellular mitochondria in vivo. Technetium-99m (Tc-99m) radiopharmaceuticals, widely used in SPECT imaging, may offer a clinically compatible solution. Cryopreserved mitochondria derived from HEK-293 cells were incubated with Tc-99m sestamibi, tetrofosmin, pertechnetate, or control solutions. After brief incubation and washing, mitochondrial pellets were analyzed for retained radioactivity. ATP content was measured to assess metabolic function, and electron microscopy was used to evaluate ultrastructural integrity. Tc-99m sestamibi and tetrofosmin showed labeling efficiencies of 2.74% and 2.68%, respectively. Pertechnetate demonstrated minimal uptake (0.34%). Radiolabeled mitochondria retained ATP production comparable to controls. Electron microscopy showed preserved double membranes and cristae. Controls confirmed assay specificity and viability. To our knowledge, this is the first report of radiolabeling isolated mitochondria with clinically approved Tc-99m agents. This platform supports the development of SPECT-compatible protocols for visualizing viable transplanted mitochondria in recipient tissues.

cell biology↗

WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

WDR11 has been implicated in congenital hypogonadotropic hypogonadism (CHH) and Kallmann syndrome (KS), human developmental genetic disorders defined by delayed puberty and infertility. However, WDR11s role in development is poorly understood. Here we report that WDR11 modulates the Hedgehog (Hh) signalling pathway and is essential for ciliogenesis. Disruption of WDR11 expression in mouse and zebrafish results in phenotypic characteristics associated with defective Hh signalling, accompanied by dysgenesis of ciliated tissues. Wdr11 null mice also exhibit early onset obesity. We found that WDR11 shuttles from the cilium to the nucleus in response to Hh signalling. WDR11 was also observed to regulate the proteolytic processing of GLI3 and cooperate with EMX1 transcription factor to induce the expression of downstream Hh pathway genes and gonadotrophin releasing hormone production. The CHH/KS-associated human mutations result in loss-of-function of WDR11. Treatment with the Hh agonist purmorphamine partially rescued the WDR11-haploinsufficiency phenotypes. Our study reveals a novel class of ciliopathy caused by WDR11 mutations and suggests that CHH/KS may be a part of the human ciliopathy spectrum.

developmental biology↗