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PMID |
Sentence |
1 |
35081502
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Spop ameliorates diabetic nephropathy through restraining NLRP3 inflammasome.
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2 |
35081502
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In the present study, an E3 ubiquitin ligase Speckle-type BTB-POZ protein (Spop) was identified as a suppressor of NLRP3 inflammasome.
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3 |
35081502
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Furthermore, Spop specific ablation in podocytes dramatically facilitated inflammatory response in glomeruli of DN mice via enhancing NLRP3 inflammasome and nuclear factor κB (NF-κB) signaling pathways, which were confirmed in HG-cultured podocytes.
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4 |
35081502
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Notably, our findings indicated that Spop directly interacted with NLRP3.
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5 |
35081502
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More importantly, Spop promoted NLRP3 degradation via elevating K48-linked polyubiquitination of NLRP3.
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6 |
35081502
|
Collectively, our findings disclosed a mechanisms through which Spop limited NLRP3 inflammasome under HG condition, and illustrated that Spop may be a novel therapeutic target to suppress NLRP3 inflammasome, contributing to the DN management.
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7 |
35081502
|
Spop ameliorates diabetic nephropathy through restraining NLRP3 inflammasome.
|
8 |
35081502
|
In the present study, an E3 ubiquitin ligase Speckle-type BTB-POZ protein (Spop) was identified as a suppressor of NLRP3 inflammasome.
|
9 |
35081502
|
Furthermore, Spop specific ablation in podocytes dramatically facilitated inflammatory response in glomeruli of DN mice via enhancing NLRP3 inflammasome and nuclear factor κB (NF-κB) signaling pathways, which were confirmed in HG-cultured podocytes.
|
10 |
35081502
|
Notably, our findings indicated that Spop directly interacted with NLRP3.
|
11 |
35081502
|
More importantly, Spop promoted NLRP3 degradation via elevating K48-linked polyubiquitination of NLRP3.
|
12 |
35081502
|
Collectively, our findings disclosed a mechanisms through which Spop limited NLRP3 inflammasome under HG condition, and illustrated that Spop may be a novel therapeutic target to suppress NLRP3 inflammasome, contributing to the DN management.
|
13 |
35081502
|
Spop ameliorates diabetic nephropathy through restraining NLRP3 inflammasome.
|
14 |
35081502
|
In the present study, an E3 ubiquitin ligase Speckle-type BTB-POZ protein (Spop) was identified as a suppressor of NLRP3 inflammasome.
|
15 |
35081502
|
Furthermore, Spop specific ablation in podocytes dramatically facilitated inflammatory response in glomeruli of DN mice via enhancing NLRP3 inflammasome and nuclear factor κB (NF-κB) signaling pathways, which were confirmed in HG-cultured podocytes.
|
16 |
35081502
|
Notably, our findings indicated that Spop directly interacted with NLRP3.
|
17 |
35081502
|
More importantly, Spop promoted NLRP3 degradation via elevating K48-linked polyubiquitination of NLRP3.
|
18 |
35081502
|
Collectively, our findings disclosed a mechanisms through which Spop limited NLRP3 inflammasome under HG condition, and illustrated that Spop may be a novel therapeutic target to suppress NLRP3 inflammasome, contributing to the DN management.
|
19 |
35081502
|
Spop ameliorates diabetic nephropathy through restraining NLRP3 inflammasome.
|
20 |
35081502
|
In the present study, an E3 ubiquitin ligase Speckle-type BTB-POZ protein (Spop) was identified as a suppressor of NLRP3 inflammasome.
|
21 |
35081502
|
Furthermore, Spop specific ablation in podocytes dramatically facilitated inflammatory response in glomeruli of DN mice via enhancing NLRP3 inflammasome and nuclear factor κB (NF-κB) signaling pathways, which were confirmed in HG-cultured podocytes.
|
22 |
35081502
|
Notably, our findings indicated that Spop directly interacted with NLRP3.
|
23 |
35081502
|
More importantly, Spop promoted NLRP3 degradation via elevating K48-linked polyubiquitination of NLRP3.
|
24 |
35081502
|
Collectively, our findings disclosed a mechanisms through which Spop limited NLRP3 inflammasome under HG condition, and illustrated that Spop may be a novel therapeutic target to suppress NLRP3 inflammasome, contributing to the DN management.
|
25 |
35081502
|
Spop ameliorates diabetic nephropathy through restraining NLRP3 inflammasome.
|
26 |
35081502
|
In the present study, an E3 ubiquitin ligase Speckle-type BTB-POZ protein (Spop) was identified as a suppressor of NLRP3 inflammasome.
|
27 |
35081502
|
Furthermore, Spop specific ablation in podocytes dramatically facilitated inflammatory response in glomeruli of DN mice via enhancing NLRP3 inflammasome and nuclear factor κB (NF-κB) signaling pathways, which were confirmed in HG-cultured podocytes.
|
28 |
35081502
|
Notably, our findings indicated that Spop directly interacted with NLRP3.
|
29 |
35081502
|
More importantly, Spop promoted NLRP3 degradation via elevating K48-linked polyubiquitination of NLRP3.
|
30 |
35081502
|
Collectively, our findings disclosed a mechanisms through which Spop limited NLRP3 inflammasome under HG condition, and illustrated that Spop may be a novel therapeutic target to suppress NLRP3 inflammasome, contributing to the DN management.
|
31 |
35081502
|
Spop ameliorates diabetic nephropathy through restraining NLRP3 inflammasome.
|
32 |
35081502
|
In the present study, an E3 ubiquitin ligase Speckle-type BTB-POZ protein (Spop) was identified as a suppressor of NLRP3 inflammasome.
|
33 |
35081502
|
Furthermore, Spop specific ablation in podocytes dramatically facilitated inflammatory response in glomeruli of DN mice via enhancing NLRP3 inflammasome and nuclear factor κB (NF-κB) signaling pathways, which were confirmed in HG-cultured podocytes.
|
34 |
35081502
|
Notably, our findings indicated that Spop directly interacted with NLRP3.
|
35 |
35081502
|
More importantly, Spop promoted NLRP3 degradation via elevating K48-linked polyubiquitination of NLRP3.
|
36 |
35081502
|
Collectively, our findings disclosed a mechanisms through which Spop limited NLRP3 inflammasome under HG condition, and illustrated that Spop may be a novel therapeutic target to suppress NLRP3 inflammasome, contributing to the DN management.
|