Gabriela Desdín-Micó

ORCID: 0000-0001-8136-4145
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About
Contact & Profiles
Research Areas
  • Pluripotent Stem Cells Research
  • CRISPR and Genetic Engineering
  • Epigenetics and DNA Methylation
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Immune cells in cancer
  • RNA modifications and cancer
  • Pancreatic function and diabetes
  • RNA Interference and Gene Delivery
  • Aortic Disease and Treatment Approaches
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Cancer-related molecular mechanisms research
  • Autophagy in Disease and Therapy
  • 3D Printing in Biomedical Research
  • Metabolism and Genetic Disorders
  • Immune Response and Inflammation
  • Mitochondrial Function and Pathology
  • Extracellular vesicles in disease
  • Tissue Engineering and Regenerative Medicine
  • Genetics and Neurodevelopmental Disorders
  • Adipose Tissue and Metabolism
  • Atherosclerosis and Cardiovascular Diseases
  • Aortic aneurysm repair treatments
  • Connective tissue disorders research
  • Circular RNAs in diseases
  • Neurogenesis and neuroplasticity mechanisms

University of Lausanne
2022-2024

Universidad Autónoma de Madrid
2017-2021

Centro de Biología Molecular Severo Ochoa
2017-2021

Consejo Superior de Investigaciones Científicas
2020-2021

Research Institute Hospital 12 de Octubre
2016-2021

Hospital Universitario 12 De Octubre
2018

The effect of immunometabolism on age-associated diseases remains uncertain. In this work, we show that T cells with dysfunctional mitochondria owing to mitochondrial transcription factor A (TFAM) deficiency act as accelerators senescence. mice, these instigate multiple aging-related features, including metabolic, cognitive, physical, and cardiovascular alterations, which together result in premature death. cell metabolic failure induces the accumulation circulating cytokines, resembles...

10.1126/science.aax0860 article EN Science 2020-05-21

Different microRNAs (miRNAs), including miR-29 family, may play a role in the development of heart failure (HF), but underlying molecular mechanisms HF pathogenesis remain unclear. We aimed at characterizing mice deficient order to address functional relevance this family miRNAs cardiovascular system and its contribution disease. In work, we show that miR-29a/b1 develop vascular remodeling systemic hypertension, as well with preserved ejection fraction (HFpEF) characterized by myocardial...

10.1371/journal.pbio.2006247 article EN cc-by PLoS Biology 2018-10-22

Aging is the major risk factor for most human diseases and represents a socio-economical challenge modern societies. Despite its importance, process of aging remains poorly understood. Epigenetic dysregulation has been proposed as key driver process. Modifications in transcriptional networks chromatin structure might be central to age-related functional decline. A prevalent feature described during overall reduction heterochromatin, specifically marked by loss repressive histone...

10.1101/2024.07.24.604929 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-07-24

Unlike aged somatic cells, which exhibit a decline in molecular fidelity and eventually reach state of replicative senescence, pluripotent stem cells can indefinitely replenish themselves while retaining full homeostatic capacity. The conferment beneficial-pluripotency related traits via

10.3389/fragi.2023.1323194 article EN cc-by Frontiers in Aging 2024-01-22

Summary In vivo reprogramming through the forced expression of Oct4, Sox2, Klf4, and c-Myc (OSKM) has demonstrated great potential for reversing age-associated phenotypes, as combination these transcription factors actively promote cell regeneration rejuvenation in various tissues organs. However, continuous OSKM raised safety concerns due to loss identity, decrease body weight, premature death. Although cyclic short-term or targeted can mitigate some detrimental effects mice, systemic wild...

10.1101/2024.03.08.584074 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-03-08

SUMMARY The induction of cellular reprogramming by forced expression the transcription factors OCT4, SOX2, KLF4, and C-MYC (OSKM) has been shown to allow dedifferentiation somatic cells ameliorate age-associated phenotypes in multiple tissues organs. Yet date, benefits vivo are limited occurrence detrimental side-effects. Here, using complementary genetic approaches, we demonstrated that continuous leads hepatic intestinal dysfunction resulting decreased body weight premature death. By...

10.1101/2022.05.27.493700 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-05-27

Abstract Unlike aged somatic cells, which exhibit a decline in molecular fidelity and eventually reach state of replicative senescence, pluripotent stem cells can indefinitely replenish themselves while retaining full homeostatic capacity. The conferment beneficial-pluripotency related traits via vivo partial cellular reprogramming (IVPR) significantly extends lifespan restores aging phenotypes mouse models. Although the phases are well characterized, details rejuvenation processes poorly...

10.1101/2023.05.12.540500 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-05-14

Abstract Age-associated neurodegenerative disorders represent significant challenges due to progressive neuronal decline and limited treatments. In aged mice, partial reprogramming, characterized by pulsed expression of reprogramming factors, has shown promise in improving function various tissues, but its impact on the aging brain remains poorly understood. Here we investigated vivo mature neurons dentate gyrus young mice. Using two different approaches – a neuron-specific transgenic...

10.1101/2024.07.24.604939 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-07-24

<title>Abstract</title> Aging is the major risk factor for most human diseases and represents a socio-economical challenge modern societies. Despite its importance, process of aging remains poorly understood. Epigenetic dysregulation has been proposed as key driver process. Alterations in transcriptional networks chromatin structure might be central to age-related functional decline. A prevalent feature described during overall reduction heterochromatin, specifically marked by loss...

10.21203/rs.3.rs-4012025/v1 preprint EN cc-by Research Square (Research Square) 2024-12-16
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