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Mesencephalic astrocyte-derived neurotrophic factor attenuates acute lung injury via inhibiting macrophages’ activation - 27/05/22

Doi : 10.1016/j.biopha.2022.112943 
Qi-ying Shen a, b, c, 1, Dong Wang d, 1, Han-yang Xu d, e, Chuan-sheng Wei d, e, Xue-ying Xiao b, Jun Liu d, e, Yu-jun Shen d, e, Lei Fang f, Li-jie Feng d, e, Yu-xian Shen d, e,
a Department of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China 
b Department of Anesthesiology, the Fourth Affiliated Hospital of Anhui Medical University, Hefei 230000, China 
c Key Laboratory of Anesthesiology and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University, Hefei 230022, China 
d School of Basic Medical Sciences, Anhui Medical University, Hefei, Anhui 230032, China 
e Biopharmaceutical Research Institute, Anhui Medical University, Hefei 230032,China 
f Department of Geriatric Respiratory and Critical Care, the First Affiliated Hospital of Anhui Medical University, Hefei 230032, China 

Corresponding author at: School of Basic Medical Sciences, Anhui Medical University, Hefei, Anhui 230032, China. School of Basic Medical Sciences, Anhui Medical University Hefei Anhui 230032 China

Abstract

Acute lung injury (ALI) is an urgent respiratory disease without effective treatment. Mesencephalic astrocyte-derived neurotrophic factor (MANF)has been demonstrated to play a suppressive role in some inflammatory conditions. However, the effect of MANF on ALI has not yet been reported. In this study, we collected bronchoalveolar lavage fluid (BALF) from the patients with or without pulmonary inflammation, and used lipopolysaccharide (LPS) to induce mice ALI model. Mono-macrophage-specific MANF knockout (MKO) mice were constructed and recombinant human MANF protein was used to ALI mice. We found that the endogenous MANF protein in both human BALF and mice lung tissues was increased in inflammatory conditions. MANF level in the macrophages of inflammatory lung was higher than that in normal controls in both human and mice. MANF deficiency in macrophages induced lung inflammation and aggravated LPS-induced lung injury. MANF lowered LPS-induced lung injury, inhibited macrophage polarization to M1 functional type. Meanwhile, MANF inhibited-LPS induced activation of NF-κB signal pathway by down regulating phosphorylated p65in lung tissue and macrophages. These results indicate that MANF acts as a suppressor in ALI via negatively regulating NF-κB activation and macrophages polarization, which may be a novel potential target and shed light on ALI therapy.

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Graphical Abstract




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Highlights

MANF was up-regulated in inflammatory lung injury.
MANF deficiency in macrophages induced lung inflammation and aggravated LPS-induced lung injury in mice.
Recombinant human MANF attenuated LPS-induced lung injury in mice.
MANF deficiency in macrophages promoted macrophages to M1differentiation in lung tissues of ALI mice.
Recombinant human MANF restricted macrophages to M1 differentiation in lung tissues of ALI mice.

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Keywords : Mesencephalic astrocyte-derived neurotrophic factor, Acute lung injury, Macrophage, NF-κB signal pathway


Esquema


 Clinical trial number: ChiCTR1800017141 (registered at Chinese Clinical Trial Registry).


© 2022  The Authors. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
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