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The RNA-Binding Protein HuR Posttranscriptionally Regulates IL-2 Homeostasis and CD4+ Th2 Differentiation

  • Patsharaporn Techasintana
  • , Jason S. Ellis
  • , Jacqueline Glascock
  • , Matthew M. Gubin
  • , Suzanne E. Ridenhour
  • , Joseph D. Magee
  • , Marcia L. Hart
  • , Peng Yao
  • , Hao Zhou
  • , Maryln S. Whitney
  • , Craig L. Franklin
  • , Jennifer L. Martindale
  • , Myriam Gorospe
  • , Wade J. Davis
  • , Paul L. Fox
  • , Xiaoxia Li
  • , Ulus Atasoy
  • University of Missouri School of Medicine
  • University of Missouri
  • Cleveland Clinic Foundation
  • National Institute On Aging

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

Posttranscriptional gene regulation by RNA-binding proteins, such as HuR (elavl1), fine-tune gene expression in T cells, leading to powerful effects on immune responses. HuR can stabilize target mRNAs and/or promote translation by interacting with their 39 untranslated region adenylate and uridylate–rich elements. It was previously demonstrated that HuR facilitates Th2 cytokine expression by mRNA stabilization. However, its effects upon IL-2 homeostasis and CD4+ Th2 differentiation are not as well understood. We found that optimal translation of Il2ra (CD25) required interaction of its mRNA with HuR. Conditional HuR knockout in CD4+ T cells resulted in loss of IL-2 homeostasis and defects in JAK–STAT signaling, Th2 differentiation, and cytokine production. HuR-knockout CD4+ T cells from OVA-immunized mice also failed to proliferate in response to Ag. These results demonstrate that HuR plays a pivotal role in maintaining normal IL-2 homeostasis and initiating CD4+ Th2 differentiation.

Original languageEnglish
Pages (from-to)109-123
Number of pages15
JournalImmunoHorizons
Volume1
Issue number6
DOIs
Publication statusPublished - 1 Aug 2017
Externally publishedYes

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