Cargando…
Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response
BACKGROUND: Previous findings indicate that susceptibility to Leishmania (Viannia) panamensis infection of monocyte-derived macrophages from patients and asymptomatically infected individuals were associated with the adaptive immune response and clinical outcome. METHODOLOGY/PRINCIPAL FINDINGS: To u...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493378/ https://www.ncbi.nlm.nih.gov/pubmed/23145196 http://dx.doi.org/10.1371/journal.pntd.0001866 |
_version_ | 1782249255703937024 |
---|---|
author | Ramírez, Carolina Díaz-Toro, Yira Tellez, Jair Castilho, Tiago M. Rojas, Ricardo Ettinger, Nicholas A. Tikhonova, Irina Alexander, Neal D. Valderrama, Liliana Hager, Janet Wilson, Mary E. Lin, Aiping Zhao, Hongyu Saravia, Nancy G. McMahon-Pratt, Diane |
author_facet | Ramírez, Carolina Díaz-Toro, Yira Tellez, Jair Castilho, Tiago M. Rojas, Ricardo Ettinger, Nicholas A. Tikhonova, Irina Alexander, Neal D. Valderrama, Liliana Hager, Janet Wilson, Mary E. Lin, Aiping Zhao, Hongyu Saravia, Nancy G. McMahon-Pratt, Diane |
author_sort | Ramírez, Carolina |
collection | PubMed |
description | BACKGROUND: Previous findings indicate that susceptibility to Leishmania (Viannia) panamensis infection of monocyte-derived macrophages from patients and asymptomatically infected individuals were associated with the adaptive immune response and clinical outcome. METHODOLOGY/PRINCIPAL FINDINGS: To understand the basis for this difference we examined differential gene expression of human monocyte-derived macrophages following exposure to L. (V.) panamensis. Gene activation profiles were determined using macrophages from healthy volunteers cultured with or without stationary phase promastigotes of L. (V.) panamensis. Significant changes in expression (>1.5-fold change; p<0.05; up- or down-regulated) were identified at 0.5, 4 and 24 hours. mRNA abundance profiles varied over time, with the highest level of activation occurring at earlier time points (0.5 and 4 hrs). In contrast to observations for other Leishmania species, most significantly changed mRNAs were up- rather than down-regulated, especially at early time points. Up-regulated transcripts over the first 24 hours belonged to pathways involving eicosanoid metabolism, oxidative stress, activation of PKC through G protein coupled receptors, or mechanism of gene regulation by peroxisome proliferators via PPARα. Additionally, a marked activation of Toll-receptor mediated pathways was observed. Comparison with published microarray data from macrophages infected with L. (Leishmania) chagasi indicate differences in the regulation of genes involved in signaling, motility and the immune response. CONCLUSIONS: Results show that the early (0.5 to 24 hours) human monocyte-derived macrophage response to L. (Viannia) panamensis is not quiescent, in contrast to published reports examining later response times (48–96 hours). Early macrophage responses are important for the developing cellular response at the site of infection. The kinetics and the mRNA abundance profiles induced by L. (Viannia) panamensis illustrate the dynamics of these interactions and the distinct biologic responses to different Leishmania species from the outset of infection within their primary host cell. |
format | Online Article Text |
id | pubmed-3493378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34933782012-11-09 Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response Ramírez, Carolina Díaz-Toro, Yira Tellez, Jair Castilho, Tiago M. Rojas, Ricardo Ettinger, Nicholas A. Tikhonova, Irina Alexander, Neal D. Valderrama, Liliana Hager, Janet Wilson, Mary E. Lin, Aiping Zhao, Hongyu Saravia, Nancy G. McMahon-Pratt, Diane PLoS Negl Trop Dis Research Article BACKGROUND: Previous findings indicate that susceptibility to Leishmania (Viannia) panamensis infection of monocyte-derived macrophages from patients and asymptomatically infected individuals were associated with the adaptive immune response and clinical outcome. METHODOLOGY/PRINCIPAL FINDINGS: To understand the basis for this difference we examined differential gene expression of human monocyte-derived macrophages following exposure to L. (V.) panamensis. Gene activation profiles were determined using macrophages from healthy volunteers cultured with or without stationary phase promastigotes of L. (V.) panamensis. Significant changes in expression (>1.5-fold change; p<0.05; up- or down-regulated) were identified at 0.5, 4 and 24 hours. mRNA abundance profiles varied over time, with the highest level of activation occurring at earlier time points (0.5 and 4 hrs). In contrast to observations for other Leishmania species, most significantly changed mRNAs were up- rather than down-regulated, especially at early time points. Up-regulated transcripts over the first 24 hours belonged to pathways involving eicosanoid metabolism, oxidative stress, activation of PKC through G protein coupled receptors, or mechanism of gene regulation by peroxisome proliferators via PPARα. Additionally, a marked activation of Toll-receptor mediated pathways was observed. Comparison with published microarray data from macrophages infected with L. (Leishmania) chagasi indicate differences in the regulation of genes involved in signaling, motility and the immune response. CONCLUSIONS: Results show that the early (0.5 to 24 hours) human monocyte-derived macrophage response to L. (Viannia) panamensis is not quiescent, in contrast to published reports examining later response times (48–96 hours). Early macrophage responses are important for the developing cellular response at the site of infection. The kinetics and the mRNA abundance profiles induced by L. (Viannia) panamensis illustrate the dynamics of these interactions and the distinct biologic responses to different Leishmania species from the outset of infection within their primary host cell. Public Library of Science 2012-10-25 /pmc/articles/PMC3493378/ /pubmed/23145196 http://dx.doi.org/10.1371/journal.pntd.0001866 Text en © 2012 Ramírez et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ramírez, Carolina Díaz-Toro, Yira Tellez, Jair Castilho, Tiago M. Rojas, Ricardo Ettinger, Nicholas A. Tikhonova, Irina Alexander, Neal D. Valderrama, Liliana Hager, Janet Wilson, Mary E. Lin, Aiping Zhao, Hongyu Saravia, Nancy G. McMahon-Pratt, Diane Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response |
title | Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response |
title_full | Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response |
title_fullStr | Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response |
title_full_unstemmed | Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response |
title_short | Human Macrophage Response to L. (Viannia) panamensis: Microarray Evidence for an Early Inflammatory Response |
title_sort | human macrophage response to l. (viannia) panamensis: microarray evidence for an early inflammatory response |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493378/ https://www.ncbi.nlm.nih.gov/pubmed/23145196 http://dx.doi.org/10.1371/journal.pntd.0001866 |
work_keys_str_mv | AT ramirezcarolina humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT diaztoroyira humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT tellezjair humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT castilhotiagom humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT rojasricardo humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT ettingernicholasa humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT tikhonovairina humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT alexanderneald humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT valderramaliliana humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT hagerjanet humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT wilsonmarye humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT linaiping humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT zhaohongyu humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT saravianancyg humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse AT mcmahonprattdiane humanmacrophageresponsetolvianniapanamensismicroarrayevidenceforanearlyinflammatoryresponse |