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1.
Mol Ther ; 29(1): 365-375, 2021 01 06.
Artículo en Inglés | MEDLINE | ID: mdl-32956626

RESUMEN

Diabetic nephropathy (DN) is a major cause of end-stage renal disease, but treatment remains ineffective. C-reactive protein (CRP) is pathogenic in DN, which significantly correlated with dipeptidyl peptidase-4 (DPP4) expression in diabetic patients with unknown reason. Here, using our unique CRPtg-db/db mice, we observed human CRP markedly induced renal DPP4 associated with enhanced kidney injury compared with db/db mice. Interestingly, linagliptin, a US Food and Drug Administration (FDA)-approved specific DPP4 inhibitor, effectively blocked this CRP-driven DN in the CRPtg-db/db mice. Mechanistically, CRP evoked DPP4 in cultured renal tubular epithelial cells, where CD32b/nuclear factor κB (NF-κB) signaling markedly enriched p65 binding on the DPP4 promoter region to increase its transcription. Unexpectedly, we further discovered that CRP triggers dimerization of DPP4 with CD32b at protein level, forming a novel DPP4/CD32b/NF-κB signaling circuit for promoting CRP-mediated DN. More importantly, linagliptin effectively blocked the circuit, thereby inhibiting the CRP/CD32b/NF-κB-driven renal inflammation and fibrosis. Thus, DPP4 may represent a precise druggable target for CRP-driven DN.


Asunto(s)
Proteína C-Reactiva/metabolismo , Nefropatías Diabéticas/metabolismo , Dipeptidil Peptidasa 4/metabolismo , FN-kappa B/metabolismo , Receptores de IgG/metabolismo , Transducción de Señal , Animales , Biomarcadores , Diabetes Mellitus Experimental , Nefropatías Diabéticas/etiología , Nefropatías Diabéticas/patología , Modelos Animales de Enfermedad , Susceptibilidad a Enfermedades , Regulación de la Expresión Génica , Ratones
2.
J Vis Exp ; (131)2018 01 09.
Artículo en Inglés | MEDLINE | ID: mdl-29364233

RESUMEN

Natural killer (NK) cells belong to the innate immune system and are a first-line anti-cancer immune defense; however, they are suppressed in the tumor microenvironment and the underlying mechanism is still largely unknown. The lack of a consistent and reliable source of NK cells limits the research progress of NK cell immunity. Here, we report an in vitro system that can provide high quality and quantity of bone marrow-derived murine NK cells under a feeder-free condition. More importantly, we also demonstrate that siRNA-mediated gene silencing successfully inhibits the E4bp4-dependent NK cell maturation by using this system. Thus, this novel in vitro NK cell differentiating system is a biomaterial solution for immunity research.


Asunto(s)
Técnicas Citológicas/métodos , Células Asesinas Naturales/citología , Animales , Factores de Transcripción con Cremalleras de Leucina de Carácter Básico/antagonistas & inhibidores , Células de la Médula Ósea/citología , Diferenciación Celular/fisiología , Línea Celular , Silenciador del Gen , Células Asesinas Naturales/fisiología , Ratones , ARN Interferente Pequeño/administración & dosificación , ARN Interferente Pequeño/genética
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