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Tissue-specific signatures in tick cell line MS profiles
BACKGROUND: The availability of tick in vitro cell culture systems has facilitated many aspects of tick research, including proteomics. However, certain cell lines have shown a tissue-specific response to infection. Thus, a more thorough characterization of tick cell lines is necessary. Proteomic co...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503378/ https://www.ncbi.nlm.nih.gov/pubmed/31060584 http://dx.doi.org/10.1186/s13071-019-3460-5 |
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author | Loginov, Dmitry S. Loginova, Yana F. Dycka, Filip Böttinger, Katharina Vechtova, Pavlina Sterba, Jan |
author_facet | Loginov, Dmitry S. Loginova, Yana F. Dycka, Filip Böttinger, Katharina Vechtova, Pavlina Sterba, Jan |
author_sort | Loginov, Dmitry S. |
collection | PubMed |
description | BACKGROUND: The availability of tick in vitro cell culture systems has facilitated many aspects of tick research, including proteomics. However, certain cell lines have shown a tissue-specific response to infection. Thus, a more thorough characterization of tick cell lines is necessary. Proteomic comparative studies of various tick cell lines will contribute to more efficient application of tick cell lines as model systems for investigation of host-vector-pathogen interactions. RESULTS: Three cell lines obtained from a hard tick, Ixodes ricinus, and two from I. scapularis were investigated. A cell mass spectrometry approach (MALDI-TOF MS) was applied, as well as classical proteomic workflows. Using PCA, tick cell line MS profiles were grouped into three clusters comprising IRE/CTVM19 and ISE18, IRE11 and IRE/CTVM20, and ISE6 cell lines. Two other approaches confirmed the results of PCA: in-solution digestion followed by nanoLC-ESI-Q-TOF MS/MS and 2D electrophoresis. The comparison of MS spectra of the cell lines and I. ricinus tick organs revealed 29 shared peaks. Of these, five were specific for ovaries, three each for gut and salivary glands, and one for Malpighian tubules. For the first time, characteristic peaks in MS profiles of tick cell lines were assigned to proteins identified in acidic extracts of corresponding cell lines. CONCLUSIONS: Several organ-specific MS signals were revealed in the profiles of tick cell lines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3460-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6503378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65033782019-05-10 Tissue-specific signatures in tick cell line MS profiles Loginov, Dmitry S. Loginova, Yana F. Dycka, Filip Böttinger, Katharina Vechtova, Pavlina Sterba, Jan Parasit Vectors Research BACKGROUND: The availability of tick in vitro cell culture systems has facilitated many aspects of tick research, including proteomics. However, certain cell lines have shown a tissue-specific response to infection. Thus, a more thorough characterization of tick cell lines is necessary. Proteomic comparative studies of various tick cell lines will contribute to more efficient application of tick cell lines as model systems for investigation of host-vector-pathogen interactions. RESULTS: Three cell lines obtained from a hard tick, Ixodes ricinus, and two from I. scapularis were investigated. A cell mass spectrometry approach (MALDI-TOF MS) was applied, as well as classical proteomic workflows. Using PCA, tick cell line MS profiles were grouped into three clusters comprising IRE/CTVM19 and ISE18, IRE11 and IRE/CTVM20, and ISE6 cell lines. Two other approaches confirmed the results of PCA: in-solution digestion followed by nanoLC-ESI-Q-TOF MS/MS and 2D electrophoresis. The comparison of MS spectra of the cell lines and I. ricinus tick organs revealed 29 shared peaks. Of these, five were specific for ovaries, three each for gut and salivary glands, and one for Malpighian tubules. For the first time, characteristic peaks in MS profiles of tick cell lines were assigned to proteins identified in acidic extracts of corresponding cell lines. CONCLUSIONS: Several organ-specific MS signals were revealed in the profiles of tick cell lines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3460-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-06 /pmc/articles/PMC6503378/ /pubmed/31060584 http://dx.doi.org/10.1186/s13071-019-3460-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Loginov, Dmitry S. Loginova, Yana F. Dycka, Filip Böttinger, Katharina Vechtova, Pavlina Sterba, Jan Tissue-specific signatures in tick cell line MS profiles |
title | Tissue-specific signatures in tick cell line MS profiles |
title_full | Tissue-specific signatures in tick cell line MS profiles |
title_fullStr | Tissue-specific signatures in tick cell line MS profiles |
title_full_unstemmed | Tissue-specific signatures in tick cell line MS profiles |
title_short | Tissue-specific signatures in tick cell line MS profiles |
title_sort | tissue-specific signatures in tick cell line ms profiles |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503378/ https://www.ncbi.nlm.nih.gov/pubmed/31060584 http://dx.doi.org/10.1186/s13071-019-3460-5 |
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