Search Results - "Gusella, G. Luca"
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Epithelial proliferation and cell cycle dysregulation in kidney injury and disease
Published in Kidney international (01-07-2021)“…Various cellular insults and injury to renal epithelial cells stimulate repair mechanisms to adapt and restore the organ homeostasis. Renal tubular epithelial…”
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2
The Joubert syndrome protein ARL13B binds tubulin to maintain uniform distribution of proteins along the ciliary membrane
Published in Journal of cell science (01-05-2018)“…Cilia-mediated signal transduction involves precise targeting and localization of selected molecules along the ciliary membrane. However, the molecular…”
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3
Inactivation of integrin-β1 prevents the development of polycystic kidney disease after the loss of polycystin-1
Published in Journal of the American Society of Nephrology (01-04-2015)“…Dysregulation of polycystin-1 (PC1) leads to autosomal dominant polycystic kidney disease (ADPKD), a disorder characterized by the formation of multiple…”
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4
LIM-Nebulette Reinforces Podocyte Structural Integrity by Linking Actin and Vimentin Filaments
Published in Journal of the American Society of Nephrology (01-10-2020)“…Maintenance of the intricate interdigitating morphology of podocytes is crucial for glomerular filtration. One of the key aspects of specialized podocyte…”
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5
Receptor heteromerization expands the repertoire of cannabinoid signaling in rodent neurons
Published in PloS one (03-01-2012)“…A fundamental question in G protein coupled receptor biology is how a single ligand acting at a specific receptor is able to induce a range of signaling that…”
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6
Autophagy Limits Endotoxemic Acute Kidney Injury and Alters Renal Tubular Epithelial Cell Cytokine Expression
Published in PloS one (18-03-2016)“…Sepsis related acute kidney injury (AKI) is a common in-hospital complication with a dismal prognosis. Our incomplete understanding of disease pathogenesis has…”
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7
Primary cilia dynamics instruct tissue patterning and repair of corneal endothelium
Published in Proceedings of the National Academy of Sciences - PNAS (15-02-2011)“…Primary cilia are required for several signaling pathways, but their function in cellular morphogenesis is poorly understood. Here we show that emergence of an…”
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8
Loss of polycystin-1 causes centrosome amplification and genomic instability
Published in Human molecular genetics (15-09-2008)“…Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenetic disease predominantly caused by alteration or dysregulation of the PKD1…”
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Cilium, centrosome and cell cycle regulation in polycystic kidney disease
Published in Biochimica et biophysica acta (01-10-2011)“…Polycystic kidney disease is the defining condition of a group of common life-threatening genetic disorders characterized by the bilateral formation and…”
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10
Prothymosin-α Variants Elicit Anti-HIV-1 Response via TLR4 Dependent and Independent Pathways
Published in PloS one (16-06-2016)“…Prothymosin α (ProTα) (isoform 2: iso2) is a widely distributed, small acidic protein with intracellular and extracellular-associated functions. Recently, we…”
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11
Prothymosin-α inhibits HIV-1 via Toll-like receptor 4-mediated type I interferon induction
Published in Proceedings of the National Academy of Sciences - PNAS (01-06-2010)“…Induction of type I interferons (IFN) is a central feature of innate immune responses to microbial pathogens and is mediated via Toll-like receptor…”
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12
Role of ubiquitin-like protein FAT10 in epithelial apoptosis in renal disease
Published in Journal of the American Society of Nephrology (01-04-2006)“…Dysregulated apoptosis of renal tubular epithelial cells (RTEC) is an important component of the pathogenesis of several renal diseases, including…”
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13
cGAS Activation Accelerates the Progression of Autosomal Dominant Polycystic Kidney Disease
Published in Journal of the American Society of Nephrology (01-04-2024)“…The renal immune infiltrate observed in autosomal polycystic kidney disease contributes to the evolution of the disease. Elucidating the cellular mechanisms…”
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14
HIV-1 Nef induces proliferation and anchorage-independent growth in podocytes
Published in Journal of the American Society of Nephrology (01-07-2002)“…HIV-associated nephropathy (HIVAN) is now the third leading cause of end-stage renal disease in the African American population. HIV-1 infects renal tubular…”
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15
SARS-CoV-2 viral protein ORF3A injures renal tubules by interacting with TRIM59 to induce STAT3 activation
Published in Molecular therapy (01-03-2023)“…Acute kidney injury occurs frequently in COVID-19 patients infected by the coronavirus SARS-CoV-2, and infection of kidney cells by this virus has been…”
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16
Tubular deficiency of ABCA1 augments cholesterol- and Na + -dependent effects on systemic blood pressure in male mice
Published in American journal of physiology. Renal physiology (01-02-2024)“…Dyslipidemia, with changes in plasma membrane (PM) composition, is associated with hypertension, while rising PM cholesterol induces Na channel activity. We…”
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17
Characterization of human metapneumovirus infection of myeloid dendritic cells
Published in Virology (New York, N.Y.) (05-01-2007)“…Abstract Recent in vivo studies suggest that hMPV is a poor inducer of inflammatory cytokines and that clinical symptoms may not be related to immune-mediated…”
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Integrin-β 1 is required for the renal cystogenesis caused by ciliary defects
Published in American journal of physiology. Renal physiology (01-05-2020)“…Defects in the function of primary cilia are commonly associated with the development of renal cysts. On the other hand, the intact cilium appears to…”
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19
Computational study of biomechanical drivers of renal cystogenesis
Published in Biomechanics and modeling in mechanobiology (01-08-2023)“…Renal cystogenesis is the pathological hallmark of autosomal dominant polycystic kidney disease, caused by PKD1 and PKD2 mutations. The formation of renal…”
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20
Reduced decay-accelerating factor expression promotes complement-mediated cystogenesis in murine ADPKD
Published in JCI insight (23-05-2024)“…Patients with autosomal dominant polycystic kidney disease (ADPKD), a genetic disease due to mutations of the PKD1 or PKD2 gene, show signs of complement…”
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