Elisabetta Dejana

ORCID: 0000-0003-0309-7154
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Vascular Malformations Diagnosis and Treatment
  • Intracranial Aneurysms: Treatment and Complications
  • Intracerebral and Subarachnoid Hemorrhage Research
  • Neuroscience and Neural Engineering
  • Extracellular vesicles in disease
  • Cancer, Lipids, and Metabolism
  • RNA Interference and Gene Delivery
  • Nerve injury and regeneration

IFOM
2022-2024

University of Milan
2019

Cerebral cavernous malformation (CCM) is a neurovascular familial or sporadic disease that characterised by capillary-venous cavernomas, and due to loss-of-function mutations any one of three CCM genes. Familial follows two-hit mechanism similar tumour suppressor genes, while in cavernomas only small fraction endothelial cells shows mutated We reported mouse models human patients, lining the lesions have different features from surrounding endothelium, as they express mesenchymal/stem-cell...

10.1038/s41467-019-10707-x article EN cc-by Nature Communications 2019-06-24

Cerebral cavernous malformations (CCM) are low-flow vascular lesions prone to cause severe hemorrhage-associated neurological complications. Pathogenic germline variants in CCM1, CCM2, or CCM3 can be identified nearly 100% of CCM patients with a positive family history. In line the concept that tumor-like mechanisms involved formation and growth, we here demonstrate an abnormally increased proliferation rate CCM3-deficient endothelial cells co-culture wild-type mosaic human iPSC-derived...

10.1007/s00018-022-04355-6 article EN cc-by Cellular and Molecular Life Sciences 2022-06-01

Cerebral cavernous malformations (CCM) are capillary affecting the central nervous system and commonly present with headaches, epilepsy stroke. Treatment of CCM is symptomatic, its prevention limited. often sporadic but sometimes may be multifocal and/or affect multiple family members. Heterozygous pathogenic variants in PDCD10 cause rarest apparently most severe genetic variant familial CCM. We carried out an RNA-Seq a Q-PCR validation analysis Pdcd10-silenced wild-type mouse endothelial...

10.3390/genes13060961 article EN Genes 2022-05-27

The blood-spinal cord barrier (BSCB) tightly regulates the transport of molecules from blood to spinal cord. Herein, we present an approach for transient modulation BSCB permeability and localized delivery peptides into behavior with high spatial resolution. This utilizes optical stimulation vasculature-targeted nanoparticles allows BSCB-impermeable without significant glial activation or impact on animal locomotor behavior. We demonstrate minimally invasive light using fiber in lumbar...

10.1021/acsnano.4c06030 article EN ACS Nano 2024-12-10
Coming Soon ...