Hyppää sisältöön
    • Suomeksi
    • In English
  • Suomeksi
  • In English
  • Kirjaudu
Näytä aineisto 
  •   Etusivu
  • 3. UTUCris-artikkelit
  • Rinnakkaistallenteet
  • Näytä aineisto
  •   Etusivu
  • 3. UTUCris-artikkelit
  • Rinnakkaistallenteet
  • Näytä aineisto
JavaScript is disabled for your browser. Some features of this site may not work without it.

Quantitative proteomic characterization and comparison of T helper 17 and induced regulatory T cells

John E. Eriksson; Ponnuswamy Mohanasundaram; Imran Mohammad; Inna Starskaia; Santosh D. Bhosale; Anne Rokka; Harri Lähdesmäki; Kari Nousiainen; David R. Goodlett; Fang Cheng; Zhi Chen; Robert Moulder

Quantitative proteomic characterization and comparison of T helper 17 and induced regulatory T cells

John E. Eriksson
Ponnuswamy Mohanasundaram
Imran Mohammad
Inna Starskaia
Santosh D. Bhosale
Anne Rokka
Harri Lähdesmäki
Kari Nousiainen
David R. Goodlett
Fang Cheng
Zhi Chen
Robert Moulder
Katso/Avaa
Publisher's PDF (6.863Mb)
Lataukset: 

Public Library of Science
doi:10.1371/journal.pbio.2004194
Näytä kaikki kuvailutiedot
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042719411
Tiivistelmä

T helper 17 (Th17) cells and induced regulatory T (iTreg) cells are two
subsets of T helper cells differentiated from naïve cells that play
important roles in autoimmune diseases, immune homeostasis, and tumor
immunity. The differentiation process is achieved by changes in numerous
proteins, including transcription regulators, enzymes, membrane
receptors, and cytokines, which are critical in lineage commitment. To
profile protein expression changes in Th17 and iTreg cells, we polarized
murine naïve CD4+ T (Thp) cells in vitro to Th17 and iTreg cells and
performed quantitative proteomic analysis of these cells. More than
4,000 proteins, covering almost all subcellular compartments, were
detected. Quantitative comparison of the protein expression profiles
resulted in the identification of proteins specifically expressed in the
Th17 and iTreg cells. Importantly, our combined analysis of proteome
and gene expression data revealed protein expression changes that were
not associated with changes at the transcriptional level. The present
study serves as a valuable resource that may prove useful in developing
treatment of autoimmune diseases and cancer.

Kokoelmat
  • Rinnakkaistallenteet [19207]

Turun yliopiston kirjasto | Turun yliopisto
julkaisut@utu.fi | Tietosuoja | Saavutettavuusseloste
 

 

Tämä kokoelma

JulkaisuajatTekijätNimekkeetAsiasanatTiedekuntaLaitosOppiaineYhteisöt ja kokoelmat

Omat tiedot

Kirjaudu sisäänRekisteröidy

Turun yliopiston kirjasto | Turun yliopisto
julkaisut@utu.fi | Tietosuoja | Saavutettavuusseloste