The role of TREM1 in regulating microglial polarization in sevoflurane-induced perioperative neurocognitive disorders

Microglia-mediated neuroinflammatory responses play a key role in perioperative neurocognitive disorders (PND). Triggering receptor expressed on myeloid cells-1 (TREM1) has been shown to be a key regulator of inflammation. However, its role in PND remains largely unknown. This study aimed to evaluat...

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Veröffentlicht in:Journal of neuroimmunology 2023-06, Vol.379, p.578070-578070, Article 578070
Hauptverfasser: Tang, Chunchun, Zheng, Xue, Zhong, Yuanping, Chen, Dongqin, Zhu, Yuhang, Wang, Sihui, Xiong, Liulin, Zhu, Zhaoqiong
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container_title Journal of neuroimmunology
container_volume 379
creator Tang, Chunchun
Zheng, Xue
Zhong, Yuanping
Chen, Dongqin
Zhu, Yuhang
Wang, Sihui
Xiong, Liulin
Zhu, Zhaoqiong
description Microglia-mediated neuroinflammatory responses play a key role in perioperative neurocognitive disorders (PND). Triggering receptor expressed on myeloid cells-1 (TREM1) has been shown to be a key regulator of inflammation. However, its role in PND remains largely unknown. This study aimed to evaluate the role of TREM1 in sevoflurane-induced PND. We applied AAV knockdown TREM1 in hippocampal microglia in aging mice. The mice were then subjected to neurobehavioral and biochemical testing after the intervention of sevoflurane. We found that sevoflurane inhalation can cause PND in mice, increase hippocampal TREM1 expression, polarize microglia to M1 type, upregulate TNF-α and IL-1β expression (pro-inflammatory), and inhibit TGF-β and IL-10 expression (anti-inflammatory). Knocking down TREM1 can improve sevoflurane-induced cognitive dysfunction, reduce M1 type marker iNOS, and increase M2 type marker ARG, improving the neuroinflammation. TREM1 is a target for sevoflurane-induced PND prevention. •Sevoflurane inhalation can cause Perioperative neurocognitive disorders (PND)in mice.•Sevoflurane induced neuroinflammation and cognitive dysfunction in aging mice.•Knocking down triggering receptors expressed on myeloid cells 1 (TREM1) can improve sevoflurane-induced cognitive dysfunction.•TREM1 is a target for sevoflurane and sevoflurane-induced PND prevention.
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Triggering receptor expressed on myeloid cells-1 (TREM1) has been shown to be a key regulator of inflammation. However, its role in PND remains largely unknown. This study aimed to evaluate the role of TREM1 in sevoflurane-induced PND. We applied AAV knockdown TREM1 in hippocampal microglia in aging mice. The mice were then subjected to neurobehavioral and biochemical testing after the intervention of sevoflurane. We found that sevoflurane inhalation can cause PND in mice, increase hippocampal TREM1 expression, polarize microglia to M1 type, upregulate TNF-α and IL-1β expression (pro-inflammatory), and inhibit TGF-β and IL-10 expression (anti-inflammatory). Knocking down TREM1 can improve sevoflurane-induced cognitive dysfunction, reduce M1 type marker iNOS, and increase M2 type marker ARG, improving the neuroinflammation. TREM1 is a target for sevoflurane-induced PND prevention. •Sevoflurane inhalation can cause Perioperative neurocognitive disorders (PND)in mice.•Sevoflurane induced neuroinflammation and cognitive dysfunction in aging mice.•Knocking down triggering receptors expressed on myeloid cells 1 (TREM1) can improve sevoflurane-induced cognitive dysfunction.•TREM1 is a target for sevoflurane and sevoflurane-induced PND prevention.</description><identifier>ISSN: 0165-5728</identifier><identifier>EISSN: 1872-8421</identifier><identifier>DOI: 10.1016/j.jneuroim.2023.578070</identifier><identifier>PMID: 37148600</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Inflammation - metabolism ; Mice ; Microglia ; Microglia - metabolism ; Neurocognitive Disorders - metabolism ; Neuroinflammation ; Perioperative neurocognitive disorders ; Sevoflurane ; Sevoflurane - adverse effects ; Sevoflurane - metabolism ; Triggering Receptor Expressed on Myeloid Cells-1 - metabolism ; Triggering receptors expressed on myeloid cells 1</subject><ispartof>Journal of neuroimmunology, 2023-06, Vol.379, p.578070-578070, Article 578070</ispartof><rights>2023</rights><rights>Copyright © 2023. 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Triggering receptor expressed on myeloid cells-1 (TREM1) has been shown to be a key regulator of inflammation. However, its role in PND remains largely unknown. This study aimed to evaluate the role of TREM1 in sevoflurane-induced PND. We applied AAV knockdown TREM1 in hippocampal microglia in aging mice. The mice were then subjected to neurobehavioral and biochemical testing after the intervention of sevoflurane. We found that sevoflurane inhalation can cause PND in mice, increase hippocampal TREM1 expression, polarize microglia to M1 type, upregulate TNF-α and IL-1β expression (pro-inflammatory), and inhibit TGF-β and IL-10 expression (anti-inflammatory). Knocking down TREM1 can improve sevoflurane-induced cognitive dysfunction, reduce M1 type marker iNOS, and increase M2 type marker ARG, improving the neuroinflammation. 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subjects Animals
Inflammation - metabolism
Mice
Microglia
Microglia - metabolism
Neurocognitive Disorders - metabolism
Neuroinflammation
Perioperative neurocognitive disorders
Sevoflurane
Sevoflurane - adverse effects
Sevoflurane - metabolism
Triggering Receptor Expressed on Myeloid Cells-1 - metabolism
Triggering receptors expressed on myeloid cells 1
title The role of TREM1 in regulating microglial polarization in sevoflurane-induced perioperative neurocognitive disorders
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