دورية
The Beta secretase BACE1 drives fibroblasts activation in Systemic Sclerosis through the APP/β-catenin/Notch signalling axis
| العنوان: | The Beta secretase BACE1 drives fibroblasts activation in Systemic Sclerosis through the APP/β-catenin/Notch signalling axis |
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| المؤلفون: | Wasson, Christopher W., De Lorenzis, Enrico, Clavane, Eva M., Ross, Rebecca L., Walker, Kieran A., Caballero-Ruiz, Begoña, Antinozzi, Cristina, Wells, Rebecca, Migneco, Gemma, Brown, Jane M.Y., Turvey, Samuel J., Simmons, Katie J., Riobo-Del Galdo, Natalia A., Di Luigi, Luigi, McKimmie, Clive S., Del Galdo, Francesco, Meakin, Paul J. |
| المصدر: | Journal of Investigative Dermatology; 20240101, Issue: Preprints |
| مستخلص: | The beta-amyloid precursor protein cleaving enzyme 1 (BACE1) is well known for its role in the development of Alzheimer’s disease. Recent publications, including our own, have demonstrated a role for this enzyme in other chronic diseases. The aim of this study was to investigate the role of BACE1 in the autoimmune disease systemic sclerosis (SSc). BACE1 protein levels were elevated in SSc patient skin. Inhibition of BACE1 with small molecule inhibitors or siRNA blocked SSc and fibrotic stimuli mediated fibroblast activation. Furthermore, we show that BACE1 regulation of dermal fibroblast activation is dependent on β-catenin and Notch signalling. The Neurotropic factor BDNF negatively regulates BACE1 expression and activity in dermal fibroblasts. Finally, sera from SSc patients show higher Aβ and lower BDNF levels compared to healthy controls. The ability of BACE1 to regulate SSc fibroblast activation reveals a therapeutic target in SSc. Several BACE1 inhibitors have been shown to be safe in clinical trials for Alzheimer’s disease and could be repurposed to ameliorate fibrosis progression. |
| قاعدة البيانات: | Supplemental Index |
| تدمد: | 0022202X 15231747 |
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| DOI: | 10.1016/j.jid.2024.03.024 |