NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progression
Signaling driven by nucleic acid sensors participates in interferonopathy-mediated autoimmune diseases. NLRP12, a pyrin-containing NLR protein, is a negative regulator of innate immune activation and type I interferon (IFN-I) production. Peripheral blood mononuclear cells (PBMCs) derived from system...
Main Authors: | , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
American Society for Clinical Investigation
2023-04-01
|
Series: | The Journal of Clinical Investigation |
Subjects: | |
Online Access: | https://doi.org/10.1172/JCI157272 |
_version_ | 1797634505928867840 |
---|---|
author | Yen-Po Tsao Fang-Yu Tseng Chih-Wei Chao Ming-Han Chen Yi-Chen Yeh Babamale Olarewaju Abdulkareem Se-Yi Chen Wen-Ting Chuang Pei-Ching Chang I-Chun Chen Pin-Hsuan Wang Chien-Sheng Wu Chang-Youh Tsai Szu-Ting Chen |
author_facet | Yen-Po Tsao Fang-Yu Tseng Chih-Wei Chao Ming-Han Chen Yi-Chen Yeh Babamale Olarewaju Abdulkareem Se-Yi Chen Wen-Ting Chuang Pei-Ching Chang I-Chun Chen Pin-Hsuan Wang Chien-Sheng Wu Chang-Youh Tsai Szu-Ting Chen |
author_sort | Yen-Po Tsao |
collection | DOAJ |
description | Signaling driven by nucleic acid sensors participates in interferonopathy-mediated autoimmune diseases. NLRP12, a pyrin-containing NLR protein, is a negative regulator of innate immune activation and type I interferon (IFN-I) production. Peripheral blood mononuclear cells (PBMCs) derived from systemic lupus erythematosus (SLE) patients expressed lower levels of NLRP12, with an inverse correlation with IFNA expression and high disease activity. NLRP12 expression was transcriptionally suppressed by runt-related transcription factor 1–dependent (RUNX1-dependent) epigenetic regulation under IFN-I treatment, which enhanced a negative feedback loop between low NLRP12 expression and IFN-I production. Reduced NLRP12 protein levels in SLE monocytes was linked to spontaneous activation of innate immune signaling and hyperresponsiveness to nucleic acid stimulations. Pristane-treated Nlrp12–/– mice exhibited augmented inflammation and immune responses; and substantial lymphoid hypertrophy was characterized in NLRP12-deficient lupus-prone mice. NLRP12 deficiency mediated the increase of autoantibody production, intensive glomerular IgG deposition, monocyte recruitment, and the deterioration of kidney function. These were bound in an IFN-I signature–dependent manner in the mouse models. Collectively, we reveal a remarkable link between low NLRP12 expression and lupus progression, which suggests the impact of NLRP12 on homeostasis and immune resilience. |
first_indexed | 2024-03-11T12:08:48Z |
format | Article |
id | doaj.art-65a81e97f46d49c2a8abbd68fb649183 |
institution | Directory Open Access Journal |
issn | 1558-8238 |
language | English |
last_indexed | 2024-03-11T12:08:48Z |
publishDate | 2023-04-01 |
publisher | American Society for Clinical Investigation |
record_format | Article |
series | The Journal of Clinical Investigation |
spelling | doaj.art-65a81e97f46d49c2a8abbd68fb6491832023-11-07T16:19:53ZengAmerican Society for Clinical InvestigationThe Journal of Clinical Investigation1558-82382023-04-011333NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progressionYen-Po TsaoFang-Yu TsengChih-Wei ChaoMing-Han ChenYi-Chen YehBabamale Olarewaju AbdulkareemSe-Yi ChenWen-Ting ChuangPei-Ching ChangI-Chun ChenPin-Hsuan WangChien-Sheng WuChang-Youh TsaiSzu-Ting ChenSignaling driven by nucleic acid sensors participates in interferonopathy-mediated autoimmune diseases. NLRP12, a pyrin-containing NLR protein, is a negative regulator of innate immune activation and type I interferon (IFN-I) production. Peripheral blood mononuclear cells (PBMCs) derived from systemic lupus erythematosus (SLE) patients expressed lower levels of NLRP12, with an inverse correlation with IFNA expression and high disease activity. NLRP12 expression was transcriptionally suppressed by runt-related transcription factor 1–dependent (RUNX1-dependent) epigenetic regulation under IFN-I treatment, which enhanced a negative feedback loop between low NLRP12 expression and IFN-I production. Reduced NLRP12 protein levels in SLE monocytes was linked to spontaneous activation of innate immune signaling and hyperresponsiveness to nucleic acid stimulations. Pristane-treated Nlrp12–/– mice exhibited augmented inflammation and immune responses; and substantial lymphoid hypertrophy was characterized in NLRP12-deficient lupus-prone mice. NLRP12 deficiency mediated the increase of autoantibody production, intensive glomerular IgG deposition, monocyte recruitment, and the deterioration of kidney function. These were bound in an IFN-I signature–dependent manner in the mouse models. Collectively, we reveal a remarkable link between low NLRP12 expression and lupus progression, which suggests the impact of NLRP12 on homeostasis and immune resilience.https://doi.org/10.1172/JCI157272AutoimmunityInflammation |
spellingShingle | Yen-Po Tsao Fang-Yu Tseng Chih-Wei Chao Ming-Han Chen Yi-Chen Yeh Babamale Olarewaju Abdulkareem Se-Yi Chen Wen-Ting Chuang Pei-Ching Chang I-Chun Chen Pin-Hsuan Wang Chien-Sheng Wu Chang-Youh Tsai Szu-Ting Chen NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progression The Journal of Clinical Investigation Autoimmunity Inflammation |
title | NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progression |
title_full | NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progression |
title_fullStr | NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progression |
title_full_unstemmed | NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progression |
title_short | NLRP12 is an innate immune checkpoint for repressing IFN signatures and attenuating lupus nephritis progression |
title_sort | nlrp12 is an innate immune checkpoint for repressing ifn signatures and attenuating lupus nephritis progression |
topic | Autoimmunity Inflammation |
url | https://doi.org/10.1172/JCI157272 |
work_keys_str_mv | AT yenpotsao nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT fangyutseng nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT chihweichao nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT minghanchen nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT yichenyeh nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT babamaleolarewajuabdulkareem nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT seyichen nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT wentingchuang nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT peichingchang nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT ichunchen nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT pinhsuanwang nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT chienshengwu nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT changyouhtsai nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression AT szutingchen nlrp12isaninnateimmunecheckpointforrepressingifnsignaturesandattenuatinglupusnephritisprogression |