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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Myeloperoxidase in human peripheral blood lymphocytes: Production and subcellular localization

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Author(s):
Okada, Sabrina Sayori [1] ; de Oliveira, Edson Mendes [1] ; de Araujo, Tomaz Henrique [2] ; Rodrigues, Maria Rita [3] ; Albuquerque, Renata Chaves [1] ; Mortara, Renato Arruda [4] ; Taniwaki, Noemi Nosomi [5] ; Nakaya, Helder Imoto [1, 6] ; Campa, Ana [1] ; Ramos Moreno, Ana Carolina [1]
Total Authors: 10
Affiliation:
[1] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Anal Clin & Toxicol, BR-05508 Sao Paulo, SP - Brazil
[2] Univ Fed Alfenas, Dept Ciencias Biol, BR-37130 Alfenas, MG - Brazil
[3] Univ Fed Alfenas, Fac Ciencias Farmaceut, Dept Anal Clin & Toxicol, BR-37130 Alfenas, MG - Brazil
[4] Univ Fed Sao Paulo, Dept Microbiol Imunobiol & Parasitol, BR-04023 Sao Paulo, SP - Brazil
[5] Adolfo Lutz Inst, Nucleo Microscopia Eletron, BR-01246 Sao Paulo, SP - Brazil
[6] Emory Univ, Yerkes Natl Primate Res Ctr, Emory Vaccine Ctr, Atlanta, GA 30329 - USA
Total Affiliations: 6
Document type: Journal article
Source: Cellular Immunology; v. 300, p. 18-25, FEB 2016.
Web of Science Citations: 5
Abstract

Myeloperoxidase (MPO) is an important enzyme in the front-line protection against microorganisms. In peripheral blood, it is accepted that MPO is only produced by myeloid-lineage cells. Thus, MPO presence is unexpected in lymphocytes. We showed recently that BI-lymphocytes from mice have MPO. Here, we showed that subsets of human peripheral B, CD4(+) and CD8(+) T lymphocytes express MPO. The content of MPO in lymphocytes was very low compared to neutrophils/monocytes with a preferential distribution in the nucleus and perinuclear region. Also, we performed a MPO mRNA expression analysis from human blood cells derived from microarray raw data publicly available, showing that MPO is modulated in infectious disease. MPO was increased in CD4(+) T lymphocytes from HIV chronic infection and in CD8(+) T lymphocytes from HCV-positive patients. Our study points out MPO as a multifunctional protein due to its subcellular localization and expression modulation in lymphocytes indicating alternative unknown functions for MPO in lymphocytes. (C) 2015 Elsevier Inc. All rights reserved. (AU)

FAPESP's process: 09/14632-3 - Kynurenine versus serotonergic pathway: role in the cross talking of immune cells and in the immune escape of tumors
Grantee:Ana Campa
Support Opportunities: Regular Research Grants
FAPESP's process: 10/18498-7 - New insights into the role of serum amyloid A (SAA) on obesity and insulin resistance
Grantee:Edson Mendes de Oliveira
Support Opportunities: Scholarships in Brazil - Doctorate