Extracellular sombrero vesicles are hallmarks of eosinophilic cytolytic degranulation in tissue sites of human diseases

Author:

Neves Vitor H1ORCID,Palazzi Cinthia1ORCID,Malta Kássia K1ORCID,Bonjour Kennedy12ORCID,Kneip Felipe1ORCID,Dias Felipe F3ORCID,Neves Josiane S4ORCID,Weller Peter F5ORCID,Melo Rossana C N1ORCID

Affiliation:

1. Laboratory of Cellular Biology, Department of Biology, ICB, Federal University of Juiz de Fora, UFJF , Rua José Lourenço Kelmer, Juiz de Fora, MG 36036-900 , Brazil

2. Unity of Biochemistry Membrane and Transport, Department of Cellular Biology and Infection, Institut Pasteur , 75724 Paris Cedex 15, Paris , France

3. Laboratory of Cellular Biology, Department of Biological Sciences, State University of Minas Gerais, UEMG , Avenida São Paulo 3996, Campus Ibirité, MG 32400-000 , Brazil

4. Institute of Biomedical Sciences, Federal University of Rio de Janeiro, UFRJ , Avenida Carlos Chagas Filho 373, Rio de Janeiro, RJ 21941-971 , Brazil

5. Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School , 330 Brookline Avenue, CLS 943, Boston, MA 02215 , United States

Abstract

Abstract Eosinophil sombrero vesicles are large tubular carriers resident in the cytoplasm of human eosinophils, identifiable by transmission electron microscopy, and important for immune mediator transport. Increased formation of sombrero vesicles occurs in activated eosinophils in vitro and in vivo. In tissue sites of eosinophilic cytolytic inflammation, extracellular eosinophil sombrero vesicles are noted, but their frequency and significance in eosinophil-associated diseases remain unclear. Here, we performed comprehensive quantitative transmission electron microscopy analyses and electron tomography to investigate the numbers, density, integrity, and 3-dimensional structure of eosinophil sombrero vesicles in different biopsy tissues from 5 prototypic eosinophil-associated diseases (eosinophilic chronic rhinosinusitis/nasal sinuses, ulcerative colitis/intestines, hypereosinophilic syndrome/skin, dermatitis/skin, and schistosomiasis/rectum). The morphology of extracellular eosinophil sombrero vesicles was also compared with that of cytoplasmic eosinophil sombrero vesicles, isolated by subcellular fractionation from peripheral blood eosinophils. We demonstrated that (i) eosinophil cytolysis, releasing intact sombrero vesicles and membrane-bound granules, is a consistent event in all eosinophil-associated diseases; (ii) eosinophil sombrero vesicles persist intact even after complete disintegration of all cell organelles, except granules (late cytolysis); (iii) the eosinophil sombrero vesicle population, composed of elongated, curved, and typical sombreros, and the eosinophil sombrero vesicle 3-dimensional architecture, diameter, and density remain unchanged in the extracellular matrix; (iv) free eosinophil sombrero vesicles closely associate with extracellular granules; and (v) free eosinophil sombrero vesicles also associate with externalized chromatin during eosinophil ETosis. Remarkably, eosinophil sombrero vesicles appeared on the surface of other cells, such as plasma cells. Thus, eosinophil cytolysis/ETosis can secrete intact sombrero vesicles, alongside granules, in inflamed tissues of eosinophil-associated diseases, potentially serving as propagators of eosinophil immune responses after cell death.

Funder

Lemann Foundation

Harvard University Lemann Brazil Research Fund

Conselho Nacional de Desenvolvimento Científico e Tecnológico

CNPq, Brazil

Fundação de Amparo a Pesquisa do Estado de Minas Gerais

FAPEMIG, Brazil

NIH

Publisher

Oxford University Press (OUP)

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