Characterizing the proteome of bullous pemphigoid blister fluid utilizing tandem mass tag labeling coupled with LC-MS/MS.


Journal

Archives of dermatological research
ISSN: 1432-069X
Titre abrégé: Arch Dermatol Res
Pays: Germany
ID NLM: 8000462

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 17 02 2021
accepted: 05 06 2021
revised: 03 05 2021
pubmed: 22 6 2021
medline: 28 9 2022
entrez: 21 6 2021
Statut: ppublish

Résumé

Bullous pemphigoid is an autoimmune blistering disease caused by autoantibodies against components of the cutaneous basement membrane zone. Autoantibodies lead to complement-dependent and -independent inflammation and blistering. Blister fluid is a valuable biologic resource, as it provides insight into both systemic and local microenvironment responses. Here, we utilized liquid chromatography with tandem mass spectrometry to characterize the bullous pemphigoid blister fluid proteome. We then depleted exosomes to better understand the exosomal versus non-exosomal proteome. We identified 339 proteins in the blister fluid of bullous pemphigoid patients. Gene ontology demonstrated enrichment of several key biologic processes including innate immune response, neutrophil degranulation, platelet degranulation, and complement activation. Exosome depletion resulted in a significant decrease in normalized reporter intensities of 192 proteins, consistent with our observation of a large number of exosomal proteins found in the blister fluid. We then compared the bullous pemphigoid blister fluid proteome to prior proteomic datasets in suction blister fluid, snake bites, and thermal burns, identifying 76 proteins unique to bullous pemphigoid. These include major basic protein, eosinophil peroxidase, galectin-10, and the immunoglobulin epsilon heavy constant region, consistent with tissue eosinophilia. We lastly validated several previously reported blister fluid exosomal components. Blister fluid in bullous pemphigoid contains a mixture of numerous biologic processes. While many of these processes are shared with blistering from alternative causes, we have identified several notable features unique to bullous pemphigoid.

Identifiants

pubmed: 34152480
doi: 10.1007/s00403-021-02253-8
pii: 10.1007/s00403-021-02253-8
doi:

Substances chimiques

Autoantibodies 0
Biological Products 0
Galectins 0
Proteome 0
Peroxidases EC 1.11.1.-
Eosinophil Major Basic Protein EC 3.1.27.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

921-928

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : FOR 2497

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Farzan Solimani (F)

Department of Dermatology, Venereology and Allergology, Charitèe-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität Zu Berlin and Berlin Institute of Health, Berlin, Germany.
Department of Dermatology and Allergology, Philipps University, Marburg, Germany.

Dario Didona (D)

Department of Dermatology and Allergology, Philipps University, Marburg, Germany.

Jing Li (J)

Department of Dermatology, University of Illinois at Chicago, Chicago, IL, USA.

Lei Bao (L)

Department of Dermatology, University of Illinois at Chicago, Chicago, IL, USA.

Payal M Patel (PM)

Department of Dermatology, University of Illinois at Chicago, Chicago, IL, USA.

Giulia Gasparini (G)

Department of Health Sciences and Department of Experimental Medicine, University of Genoa, Genoa, Italy.
Department of Health Sciences (DISSAL), Section of Dermatology, University of Genoa, San Martino Policlinic Hospital IRCCS, Genoa, Italy.

Khalaf Kridin (K)

Lübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.

Emanuele Cozzani (E)

Department of Health Sciences (DISSAL), Section of Dermatology, University of Genoa, San Martino Policlinic Hospital IRCCS, Genoa, Italy.

Michael Hertl (M)

Department of Dermatology and Allergology, Philipps University, Marburg, Germany.

Kyle T Amber (KT)

Division of Dermatology, Rush University Medical Center, 707 S Wood St. Suite 220, Chicago, IL, USA. kyle_amber@rush.edu.
Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA. kyle_amber@rush.edu.
Department of Otorhinolaryngology, Rush University Medical Center, Chicago, IL, 60612, USA. kyle_amber@rush.edu.

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