Publications by authors named "E Cortada"

Together with obesity and type 2 diabetes, metabolic dysfunction-associated steatotic liver disease (MASLD) is a growing global epidemic. Activation of the complement system and infiltration of macrophages has been linked to progression of metabolic liver disease. The role of complement receptors in macrophage activation and recruitment in MASLD remains poorly understood.

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The immune system coordinates the response to cardiac injury and controls regenerative and fibrotic scar outcomes in the heart and subsequent chronic low-grade inflammation associated with heart failure. Adult mice and humans lack the ability to fully recover while adult zebrafish spontaneously regenerate after heart injury. Here we profile the inflammatory response to heart cryoinjury in zebrafish and coronary artery ligation in mouse using single cell transcriptomics.

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The voltage-gated sodium (Na) channel is critical for cardiomyocyte function since it is responsible for action potential initiation and its propagation throughout the cell. It consists of a protein complex made of a pore forming α subunit and associated β subunits, which regulate α subunit function and subcellular localization. We previously showed the implication of N-linked glycosylation and S-acylation of β2 in its polarized trafficking.

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Article Synopsis
  • Metabolic dysfunction-associated steatotic liver disease (MASLD) is increasingly common alongside obesity and type 2 diabetes, with a link to immune responses involving complement proteins and macrophages.
  • The study investigates the role of the complement 3a receptor (C3aR1) in macrophages, particularly in the liver's Kupffer cells, by creating mouse models lacking this receptor.
  • Results show that deleting C3aR1 in macrophages or Kupffer cells doesn't significantly impact liver conditions like steatosis, inflammation, or fibrosis in the context of a MASLD-inducing diet.
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Thermogenesis in beige/brown adipose tissues can be leveraged to combat metabolic disorders such as type 2 diabetes and obesity. The complement system plays pleiotropic roles in metabolic homeostasis and organismal energy balance with canonical effects on immune cells and noncanonical effects on nonimmune cells. The adipsin/C3a/C3a receptor 1 (C3aR1) pathway stimulates insulin secretion and sustains pancreatic β cell mass.

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