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Notch Signaling Regulation in Autoinflammatory Diseases
被引:20
作者:
Gratton, Rossella
[1
]
Tricarico, Paola Maura
[1
]
d'Adamo, Adamo Pio
[1
,2
]
Bianco, Anna Monica
[1
]
Moura, Ronald
[1
]
Agrelli, Almerinda
[3
]
Brandao, Lucas
[1
]
Zupin, Luisa
[1
]
Crovella, Sergio
[4
]
机构:
[1] Inst Maternal & Child Hlth IRCCS Burlo Garofolo, I-34137 Trieste, Italy
[2] Univ Trieste, Dept Med Surg & Hlth Sci, I-34149 Trieste, Italy
[3] Univ Fed Pernambuco, Dept Pathol, BR-50670901 Recife, PE, Brazil
[4] Univ Qatar, Coll Arts & Sci, Dept Biol & Environm Sci, Doha 2713, Qatar
关键词:
Notch pathway;
autoinflammation;
genetic;
autoinflammatory diseases;
GIANT-CELL ARTERITIS;
HIDRADENITIS SUPPURATIVA;
INNATE IMMUNITY;
PATHWAY;
PATHOGENESIS;
GAMMA;
ACTIVATION;
MECHANISMS;
EXPRESSION;
MUTATIONS;
D O I:
10.3390/ijms21228847
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Notch pathway is a highly conserved intracellular signaling route that modulates a vast variety of cellular processes including proliferation, differentiation, migration, cell fate and death. Recently, the presence of a strict crosstalk between Notch signaling and inflammation has been described, although the precise molecular mechanisms underlying this interplay have not yet been fully unravelled. Disruptions in Notch cascade, due both to direct mutations and/or to an altered regulation in the core components of Notch signaling, might lead to hypo- or hyperactivation of Notch target genes and signaling molecules, ultimately contributing to the onset of autoinflammatory diseases. To date, alterations in Notch signaling have been reported as associated with three autoinflammatory disorders, therefore, suggesting a possible role of Notch in the pathogenesis of the following diseases: hidradenitis suppurativa (HS), Behcet disease (BD), and giant cell arteritis (GCA). In this review, we aim at better characterizing the interplay between Notch and autoinflammatory diseases, trying to identify the role of this signaling route in the context of these disorders.
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页码:1 / 13
页数:13
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