Abstract

The cytokine erythropoietin (Epo) mediates various cell homeostatic responses to environmental challenges and pathological insults. While stimulation of vertebrate erythrocyte production is mediated by homodimeric “classical” Epo receptors, alternative receptors are involved in neuroprotection. However, their identity remains enigmatic due to complex cytokine ligand and receptor interactions and conflicting experimental results. Besides the classical Epo receptor, the family of type I cytokine receptors also includes the poorly characterized orphan cytokine receptor-like factor 3 (CRLF3) present in vertebrates including human and various insect species. By making use of the more simple genetic makeup of insect model systems, we studied whether CRLF3 is a neuroprotective Epo receptor in animals. We identified a single ortholog of CRLF3 in the beetle Tribolium castaneum, and established protocols for primary neuronal cell cultures from Tribolium brains and efficient in vitro RNA interference. Recombinant human Epo as well as the non-erythropoietic Epo splice variant EV-3 increased the survival of serum-deprived brain neurons, confirming the previously described neuroprotective effect of Epo in insects. Moreover, Epo completely prevented hypoxia-induced apoptotic cell death of primary neuronal cultures. Knockdown of CRLF3 expression by RNA interference with two different double stranded RNA (dsRNA) fragments abolished the neuroprotective effect of Epo, indicating that CRLF3 is a crucial component of the insect Epo-responsive receptor. This suggests that a common urbilaterian ancestor of the orphan human and insect cytokine receptor CRLF3 served as a neuroprotective receptor for an Epo-like cytokine. Our work also suggests that vertebrate CRLF3, like its insect ortholog, might represent a tissue protection-mediating receptor.

Highlights

  • Erythropoietin (Epo) is a positive regulator of vertebrate erythropoiesis

  • Expression of classical EpoR in the brain has been demonstrated by numerous studies, Epo receptors mediating neuroprotection seem to be different from the classical homodimeric EpoR involved in erythropoiesis (Leist et al, 2004; Brines and Cerami, 2005)

  • We demonstrate that knockdown of Tc-cytokine receptor-like factor 3 (CRLF3) expression abolishes the protective effect of Epo on hypoxia-exposed T. castaneum brain neurons

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Summary

Introduction

Epo is synthesized and released as a para- or autocrine signal in various tissues that initiates adaptive cellular responses to injury and physiological challenges in order to support cell survival, maintenance of functions and regeneration (Noguchi et al, 2008; Sargin et al, 2010; Chateauvieux et al, 2011). Even within a particular tissue such as the nervous system, the expression of Epo receptors may depend on cell type, developmental stage, physiological condition and actual as well as previous exposure to challenging stimuli (Sinor and Greenberg, 2000; Brines and Cerami, 2005; Shein et al, 2005; Um et al, 2007; Sanchez et al, 2009). Cells may flexibly respond to different physiological challenges by expressing different Epo receptors that activate particular adaptive cellular responses

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