Genetic deletion of the apoptosis associated speck like protein containing a card in LysM+ macrophages attenuates spinal cord injury by regulating M1/M2 polarization through ASC-dependent inflammasome signaling axis

Apoptosis associated speck like protein containing a card (ASC), the key adaptor protein of the assembly and activation of canonical inflammasomes, has been found to play a significant role in neuroinflammation after spinal cord injury (SCI). The previous studies indicated that widely block or knock...

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Veröffentlicht in:Experimental neurology 2024-12, Vol.382, p.114982, Article 114982
Hauptverfasser: Ding, Shu-Qin, Yan, Hua-Zheng, Gao, Jian-Xiong, Chen, Yu-Qing, Zhang, Nan, Wang, Rui, Li, Jiang-Yan, Hu, Jian-Guo, Lü, He-Zuo
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container_title Experimental neurology
container_volume 382
creator Ding, Shu-Qin
Yan, Hua-Zheng
Gao, Jian-Xiong
Chen, Yu-Qing
Zhang, Nan
Wang, Rui
Li, Jiang-Yan
Hu, Jian-Guo
Lü, He-Zuo
description Apoptosis associated speck like protein containing a card (ASC), the key adaptor protein of the assembly and activation of canonical inflammasomes, has been found to play a significant role in neuroinflammation after spinal cord injury (SCI). The previous studies indicated that widely block or knockout ASC can ameliorate SCI. However, ASC is ubiquitously expressed in infiltrated macrophages and local microglia, so further exploration is needed on which type of cell playing the key role. In this study, using the LysMcre;Ascflox/flox mice with macrophage-specifc ASC conditional knockout (CKO) and contusive SCI model, we focus on evaluating the specific role of ASC in lysozyme 2 (LysM)+ myeloid cells (mainly infiltrated macrophages) in this pathology. The results revealed that macrophage-specifc Asc CKO exhibited the follow effects: (1) A significant reduction in the numbers of infiltrated macrophages in the all phases of SCI, and activated microglia in the acute and subacute phases. (2) A significant reduction in ASC, caspase-1, interleukin (IL)-1β, and IL-18 compared to control mice. (3) In the acute and subacute phases of SCI, M1 subset differentiation was inhibited, and M2 differentiation was increased. (4) Histology and hindlimb motor recoveries were improved. In conclusion, this study elucidates that macrophage-specific ASC CKO can improve nerve function recovery after SCI by regulating M1/M2 polarization through inhibiting ASC-dependent inflammasome signaling axis. This indicates that ASC in peripheral infiltrated macrophages may play an important role in SCI pathology, at least in mice, could be a potential target for treatment. [Display omitted] •Asc CKO can reduce the infiltration of macrophages after SCI in mice.•Asc CKO can reduce the activated microglia in the acute and subacute phases of SCI.•Asc CKO can inhibit ASC-dependent inflammasome signaling axis.•Asc CKO can inhibit M1 polarization, and increase M2 polarization.•Asc CKO can improve histology and hindlimb motor recoveries after SCI.
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The previous studies indicated that widely block or knockout ASC can ameliorate SCI. However, ASC is ubiquitously expressed in infiltrated macrophages and local microglia, so further exploration is needed on which type of cell playing the key role. In this study, using the LysMcre;Ascflox/flox mice with macrophage-specifc ASC conditional knockout (CKO) and contusive SCI model, we focus on evaluating the specific role of ASC in lysozyme 2 (LysM)+ myeloid cells (mainly infiltrated macrophages) in this pathology. The results revealed that macrophage-specifc Asc CKO exhibited the follow effects: (1) A significant reduction in the numbers of infiltrated macrophages in the all phases of SCI, and activated microglia in the acute and subacute phases. (2) A significant reduction in ASC, caspase-1, interleukin (IL)-1β, and IL-18 compared to control mice. (3) In the acute and subacute phases of SCI, M1 subset differentiation was inhibited, and M2 differentiation was increased. (4) Histology and hindlimb motor recoveries were improved. In conclusion, this study elucidates that macrophage-specific ASC CKO can improve nerve function recovery after SCI by regulating M1/M2 polarization through inhibiting ASC-dependent inflammasome signaling axis. This indicates that ASC in peripheral infiltrated macrophages may play an important role in SCI pathology, at least in mice, could be a potential target for treatment. [Display omitted] •Asc CKO can reduce the infiltration of macrophages after SCI in mice.•Asc CKO can reduce the activated microglia in the acute and subacute phases of SCI.•Asc CKO can inhibit ASC-dependent inflammasome signaling axis.•Asc CKO can inhibit M1 polarization, and increase M2 polarization.•Asc CKO can improve histology and hindlimb motor recoveries after SCI.</description><identifier>ISSN: 0014-4886</identifier><identifier>ISSN: 1090-2430</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2024.114982</identifier><identifier>PMID: 39353545</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Apoptosis-associated speck-like protein containing a card ; Conditional gene knockout ; LysM+ macrophages ; Spinal cord injury</subject><ispartof>Experimental neurology, 2024-12, Vol.382, p.114982, Article 114982</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. 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(4) Histology and hindlimb motor recoveries were improved. In conclusion, this study elucidates that macrophage-specific ASC CKO can improve nerve function recovery after SCI by regulating M1/M2 polarization through inhibiting ASC-dependent inflammasome signaling axis. This indicates that ASC in peripheral infiltrated macrophages may play an important role in SCI pathology, at least in mice, could be a potential target for treatment. 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(4) Histology and hindlimb motor recoveries were improved. In conclusion, this study elucidates that macrophage-specific ASC CKO can improve nerve function recovery after SCI by regulating M1/M2 polarization through inhibiting ASC-dependent inflammasome signaling axis. This indicates that ASC in peripheral infiltrated macrophages may play an important role in SCI pathology, at least in mice, could be a potential target for treatment. [Display omitted] •Asc CKO can reduce the infiltration of macrophages after SCI in mice.•Asc CKO can reduce the activated microglia in the acute and subacute phases of SCI.•Asc CKO can inhibit ASC-dependent inflammasome signaling axis.•Asc CKO can inhibit M1 polarization, and increase M2 polarization.•Asc CKO can improve histology and hindlimb motor recoveries after SCI.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39353545</pmid><doi>10.1016/j.expneurol.2024.114982</doi></addata></record>
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subjects Apoptosis-associated speck-like protein containing a card
Conditional gene knockout
LysM+ macrophages
Spinal cord injury
title Genetic deletion of the apoptosis associated speck like protein containing a card in LysM+ macrophages attenuates spinal cord injury by regulating M1/M2 polarization through ASC-dependent inflammasome signaling axis
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