A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Quantitative proteomics analysis of the nuclear fraction of human CD4+ cells in the early phases of IL-4-induced Th2 differentiation
Tekijät: Moulder R, Lönnberg T, Elo LL, Filen JJ, Rainio E, Corthals G, Oresic M, Nyman TA, Aittokallio T, Lahesmaa R
Kustantaja: ASBMB
Julkaisuvuosi: 2010
Journal: Molecular and Cellular Proteomics
Lehden akronyymi: Mol Cell Proteomics.
Artikkelin numero: M900483-MCP200
Vuosikerta: 9
Numero: 9
Aloitussivu: 1937
Lopetussivu: 1953
Sivujen määrä: 17
ISSN: 1535-9476
DOI: https://doi.org/10.1074/mcp.M900483-MCP200
Verkko-osoite: http://www.mcponline.org/content/9/9/1937.long
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/Publication/2881174
We used stable isotope labeling with 4-plex iTRAQ (isobaric tags for relative and absolute quantification) reagents and LC-MS/MS to investigate proteomic changes in the nucleus of activated human CD4(+) cells during the early stages of Th2 cell differentiation. The effects of IL-4 stimulation upon activated naïve CD4(+) cells were measured in the nuclear fractions from 6 and 24 h in three biological replicates, each using pooled cord blood samples derived from seven or more individuals. In these analyses, in the order of 800 proteins were detected with two or more peptides and quantified in three biological replicates. In addition to consistent differences observed with the nuclear localization/expression of established human Th2 and Th1 markers, there were changes that suggested the involvement of several proteins either only recently reported or otherwise not known in this context. These included SATB1 and among the novel changes detected and validated an IL-4-induced increase in the level of YB1. This unique data set from human cord blood CD4(+) T cells details an extensive list of protein determinations that compares with and complements previous data determined from the Jurkat cell nucleus.
Ladattava julkaisu This is an electronic reprint of the original article. |