Integrative lipidomic features identify plasma lipid signatures in chronic urticaria
Chronic urticaria (CU) is a chronic inflammatory skin disease mainly mediated by mast cells. Lipids exert essential functions in biological processes; however, the role of lipids in CU remains unclear. Nontargeted lipidomics was performed to investigate the differential lipid profiles between CU pat...
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Published in | Frontiers in immunology Vol. 13; p. 933312 |
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Main Authors | , , , , , , , , , |
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Abstract | Chronic urticaria (CU) is a chronic inflammatory skin disease mainly mediated by mast cells. Lipids exert essential functions in biological processes; however, the role of lipids in CU remains unclear. Nontargeted lipidomics was performed to investigate the differential lipid profiles between CU patients and healthy control (HC) subjects. Functional validation studies were performed
in vitro
and
in vivo
including β-hexosaminidase release examination from mast cells and passive cutaneous anaphylaxis (PCA) mouse model. We detected dramatically altered glycerophospholipids in CU patients compared with HCs. Phosphatidylserine (PS), phosphatidylethanolamine (PE), and phosphatidylglycerol (PG) were increased, while phosphatidylcholine (PC) was reduced in CU patients. The reduction in PC was related to a high weekly urticaria activity score (UAS7), while PS was positively associated with the dermatology life quality index (DLQI). We also identified the differential lipid profiles between chronic spontaneous urticaria (CSU), symptomatic dermographism (SD), and CSU coexist with SD. CU patients were classified into two subtypes (subtype 1 and subtype 2) based on consensus clustering of lipid profiling. Compared with patients in subtype 2, patients in subtype 1 had elevated levels of PC (18:0e/18:2) and PE (38:2), and lower urticaria control test (UCT) scores indicated worse clinical efficiency of secondary generation H1 antihistamines treatment. Importantly, we found that supplementation with PC could attenuate IgE-induced immune responses in mast cells. In general, We described the landscape of plasma lipid alterations in CU patients and provided novel insights into the role of PC in mast cells. |
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AbstractList | Chronic urticaria (CU) is a chronic inflammatory skin disease mainly mediated by mast cells. Lipids exert essential functions in biological processes; however, the role of lipids in CU remains unclear. Nontargeted lipidomics was performed to investigate the differential lipid profiles between CU patients and healthy control (HC) subjects. Functional validation studies were performed
in vitro
and
in vivo
including β-hexosaminidase release examination from mast cells and passive cutaneous anaphylaxis (PCA) mouse model. We detected dramatically altered glycerophospholipids in CU patients compared with HCs. Phosphatidylserine (PS), phosphatidylethanolamine (PE), and phosphatidylglycerol (PG) were increased, while phosphatidylcholine (PC) was reduced in CU patients. The reduction in PC was related to a high weekly urticaria activity score (UAS7), while PS was positively associated with the dermatology life quality index (DLQI). We also identified the differential lipid profiles between chronic spontaneous urticaria (CSU), symptomatic dermographism (SD), and CSU coexist with SD. CU patients were classified into two subtypes (subtype 1 and subtype 2) based on consensus clustering of lipid profiling. Compared with patients in subtype 2, patients in subtype 1 had elevated levels of PC (18:0e/18:2) and PE (38:2), and lower urticaria control test (UCT) scores indicated worse clinical efficiency of secondary generation H1 antihistamines treatment. Importantly, we found that supplementation with PC could attenuate IgE-induced immune responses in mast cells. In general, We described the landscape of plasma lipid alterations in CU patients and provided novel insights into the role of PC in mast cells. Chronic urticaria (CU) is a chronic inflammatory skin disease mainly mediated by mast cells. Lipids exert essential functions in biological processes; however, the role of lipids in CU remains unclear. Nontargeted lipidomics was performed to investigate the differential lipid profiles between CU patients and healthy control (HC) subjects. Functional validation studies were performed in vitro and in vivo including β-hexosaminidase release examination from mast cells and passive cutaneous anaphylaxis (PCA) mouse model. We detected dramatically altered glycerophospholipids in CU patients compared with HCs. Phosphatidylserine (PS), phosphatidylethanolamine (PE), and phosphatidylglycerol (PG) were increased, while phosphatidylcholine (PC) was reduced in CU patients. The reduction in PC was related to a high weekly urticaria activity score (UAS7), while PS was positively associated with the dermatology life quality index (DLQI). We also identified the differential lipid profiles between chronic spontaneous urticaria (CSU), symptomatic dermographism (SD), and CSU coexist with SD. CU patients were classified into two subtypes (subtype 1 and subtype 2) based on consensus clustering of lipid profiling. Compared with patients in subtype 2, patients in subtype 1 had elevated levels of PC (18:0e/18:2) and PE (38:2), and lower urticaria control test (UCT) scores indicated worse clinical efficiency of secondary generation H1 antihistamines treatment. Importantly, we found that supplementation with PC could attenuate IgE-induced immune responses in mast cells. In general, We described the landscape of plasma lipid alterations in CU patients and provided novel insights into the role of PC in mast cells. |
Author | Zhu, Lei Li, Liqiao Lin, Liang Liu, Runqiu Li, Jie Hou, Guixue Peng, Cong Zhou, Bingjing Xiao, Yi Chen, Xiang |
AuthorAffiliation | 2 Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University , Changsha , China 4 National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University , Changsha , China 5 BGI-Shenzhen , Shenzhen, Guangdong , China 3 Hunan Engineering Research Center of Skin Health and Disease, Xiangya Hospital, Central South University , Changsha , China 1 Department of Dermatology, Xiangya Hospital, Central South University , Changsha , China |
AuthorAffiliation_xml | – name: 2 Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University , Changsha , China – name: 1 Department of Dermatology, Xiangya Hospital, Central South University , Changsha , China – name: 5 BGI-Shenzhen , Shenzhen, Guangdong , China – name: 3 Hunan Engineering Research Center of Skin Health and Disease, Xiangya Hospital, Central South University , Changsha , China – name: 4 National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University , Changsha , China |
Author_xml | – sequence: 1 givenname: Jie surname: Li fullname: Li, Jie – sequence: 2 givenname: Liqiao surname: Li fullname: Li, Liqiao – sequence: 3 givenname: Runqiu surname: Liu fullname: Liu, Runqiu – sequence: 4 givenname: Lei surname: Zhu fullname: Zhu, Lei – sequence: 5 givenname: Bingjing surname: Zhou fullname: Zhou, Bingjing – sequence: 6 givenname: Yi surname: Xiao fullname: Xiao, Yi – sequence: 7 givenname: Guixue surname: Hou fullname: Hou, Guixue – sequence: 8 givenname: Liang surname: Lin fullname: Lin, Liang – sequence: 9 givenname: Xiang surname: Chen fullname: Chen, Xiang – sequence: 10 givenname: Cong surname: Peng fullname: Peng, Cong |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Marianna Kulka, University of Alberta, Canada These authors have contributed equally to this work and share first authorship Reviewed by: Becky Vonakis, Johns Hopkins Medicine, United States; Nami Shrestha, University of Alberta, Canada; Zuotao Zhao, Peking University, China; Jason Meyer, Vanderbilt University Medical Center, United States This article was submitted to Autoimmune and Autoinflammatory Disorders, a section of the journal Frontiers in Immunology |
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Snippet | Chronic urticaria (CU) is a chronic inflammatory skin disease mainly mediated by mast cells. Lipids exert essential functions in biological processes; however,... |
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SubjectTerms | chronic urticaria glycerophospholipid Immunology lipidomic signatures mast cell phosphatidylcholine |
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Title | Integrative lipidomic features identify plasma lipid signatures in chronic urticaria |
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