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Anti-apoptotic and neuroprotective erythropoietin/CRLF3-signalling in insects and humans

dc.contributor.advisorHeinrich, Ralf Prof. Dr.
dc.contributor.authorKnorr, Debbra Yasemin
dc.titleAnti-apoptotic and neuroprotective erythropoietin/CRLF3-signalling in insects and humansde
dc.contributor.refereeHeinrich, Ralf Prof. Dr.
dc.description.abstractengThe cytokine receptor like factor 3 (CRLF3) evolved together with the eumetazoan nervous system and is present in all major groups of Animalia. Based on sequence similarities, CRLF3 was assigned to the family of class 1 cytokine receptors which also includes the classical erythropoietin receptor (EpoR). CRLF3 misregulation has been associated with several human diseases, but neither its ligand nor a particular function have been reported. Erythropoietin (Epo) is a vertebrate-specific helical cytokine that regulates erythropoiesis and activates cytoprotective pathways in various tissues including the nervous system. Neuroprotective functions of Epo are partially mediated by EpoR but also by additional, partly unidentified receptors. In insects, CRLF3 was identified to respond to human recombinant Epo and the naturally occurring Epo splice variant EV-3. Activation of CRLF3 in insects stimulates anti-apoptotic processes via JAK/STAT intracellular signalling. Even though many efforts were made in order to characterize CRLF3-mediated responses, downstream effectors beyond JAK/STAT remained elusive. My thesis combines studies on CRLF3-mediated anti-apoptotic mechanisms in insects and the functional characterisation of human CRLF3 in iPSC (induced pluripotent stem cell) -derived neurons. Studies on Locusta migratoria and Tribolium castaneum revealed a pro-apoptotic role of acetylcholinesterase (AChE coded by ace) that was previously reported for vertebrates. Similar to those studies, reduction of AChE levels and inhibition of AChE activity prevented apoptotic death in hypoxiaexposed primary neuron cultures. Moreover, apoptogenic stimuli increased ace expression supporting the association of AChE with increased apoptosis under challenging conditions. Experiments in T. castaneum indicated that both types of AChE (AChE-1 transcribed from ace-1 and AChE-2 transcribed from ace-2) promote apoptosis and are upregulated by apoptogenic stimuli. However, stressinduced upregulation of AChE-1 was prevented by neuroprotective concentrations of Epo. This indicated that Epo/CRLF3-stimulated neuroprotection is mediated through suppression of pro-apoptotic ace-1 expression. Whether this Epo-stimulated protective mechanism is specific to insects or also present in other species remains to be studied. In order to determine the endogenous ligand of insect CRLF3 (insects do not possess Epo) I used locust hemolymph as potential source for its identification. I first demonstrated that locust hemolymph protects both L. migratoria and T. castaneum primary neurons from hypoxia-induced apoptosis. The protective effect was absent after RNAi-mediated knockdown of CRLF3 expression. Thus, locust hemolymph contains a ligand that is sufficiently conserved to activate CRLF3 in different insect species. Fractionation of locust hemolymph by size exclusion chromatography generated two (out of >11) fractions with particular neuroprotective potency. These hemolymph fractions will be used to separate and identify the CRLF3 ligand. In order to determine the function of human CRLF3, I generated CRLF3-knockout lines from two fibroblast-derived human iPSC lines by CRISPR/Cas9 gene editing. CRLF3 KO lines, along with wild type and isogenic controls, were differentiated into neuronal-like cells expressing cell type-specific markes and presenting characteristic morphology. After differentiation, neuronal-like cells were exposed to rotenone, an inhibitor of respiratory chain complex I, which induced apoptosis in all cell lines. The addition of the Epo splice variant EV-3 prevented rotenone-induced cell death in wild type and isogenic controls but not in CRLF3 KO neurons. This demonstrates that human CRLF3 is a neuroprotective receptor similar to its previously determined function in insects. Moreover, CRLF3 is identified as the first known receptor for EV-3 and vice versa, human CRLF3 is deorphanized by identifying EV-3 as one of its endogenous ligands. Taken together, my work has identifyed CRLF3 as a new player in neuroprotection that may account for various previously described Epo-mediated cytoprotective functions in the nervous system and other tissues. Specific activation of CRLF3-mediated beneficial pathways may interfere with degenerative processes without coactivation of EpoR and its associated adverse side
dc.contributor.coRefereeBucher, Gregor Prof. Dr.
dc.contributor.thirdRefereeBehr, Rüdiger Prof. Dr.
dc.contributor.thirdRefereeOuteiro, Tiago Fleming Prof. Dr.
dc.contributor.thirdRefereeBoretius, Susann Prof. Dr.
dc.contributor.thirdRefereeBradler, Sven Dr.
dc.subject.engiPSC-derived neuronsde
dc.subject.engTribolium castaneumde
dc.subject.engLocusta migratoriade
dc.subject.engEpo-like ligandde
dc.subject.engNeuroprotective hemolymphde
dc.subject.engLigand identificationde
dc.subject.engCytokine receptor like factor 3de
dc.subject.engCell protectionde
dc.affiliation.instituteBiologische Fakultät für Biologie und Psychologiede
dc.subject.gokfullBiologie (PPN619462639)de

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