Publications by authors named "C C Berthier"

The potential pathogenic role of disturbed Ca2+ homeostasis in Duchenne muscular dystrophy (DMD) remains a complex, unsettled issue. We used muscle fibers isolated from 3-mo-old DMDmdx rats to further investigate the case. Most DMDmdx fibers exhibited no sign of trophic or morphology distinction as compared with WT fibers and mitochondria and t-tubule membrane networks also showed no stringent discrepancy.

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Background: Interstitial fibrosis and tubular atrophy (IFTA), and density and shape of peritubular capillaries (PTCs), are independently prognostic of disease progression. This study aimed to identify novel digital biomarkers of disease progression and assess the clinical relevance of the interplay between a variety of PTC characteristics and their microenvironment in glomerular diseases.

Methods: A total of 344 NEPTUNE/CureGN participants were included: 112 minimal change disease, 134 focal segmental glomerulosclerosis, 61 membranous nephropathy, and 37 IgA nephropathy.

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Objective: Cutaneous lupus erythematosus (CLE) is an inflammatory skin manifestation of systemic lupus erythematosus. Type I interferons (IFNs) promote inflammatory responses and are elevated in CLE lesions. We recently reported that CLE lesions are frequently colonized with Staphylococcus aureus.

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Article Synopsis
  • Exposure to ultraviolet (UV) light is a known trigger for inflammation in systemic lupus erythematosus (SLE), but the specific cells involved in this response and how UV exposure interacts with interferons are not fully understood.
  • This study utilized a murine model of lupus, comparing responses in NZM2328 mice and iNZM mice with a type I interferon receptor knockout, as well as wild-type BALB/c mice, to investigate the effects of different UV treatments.
  • Findings showed that myeloid cells, particularly neutrophils and monocyte-derived dendritic cells, play a key role in the inflammatory response to UV exposure in lupus-prone mice, emphasizing the potential for targeting type I interferons and
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