Acta Biochimica et Biophysica Sinica · 2022 · 10 citations · 28 references
Life SciencesMolecular BiologyNeuroscienceGene ExpressionMolecular NeuroscienceTranscriptional RegulationNeurochemical Signaling PathwaysNeurotransmitter ReceptorsNuclear ReceptorsReceptor RegulationReceptor Signaling In NeuronsAdenylate Cyclase RegulationAdenylate Cyclase SignalingAllosteric Enzyme RegulationNeuroprotective MechanismsNeuroprotective SignalingNuclear Translocation Of Transcription FactorsPositive Allosteric ModulationPositive Allosteric Modulators
PAC1-R is a recognized preferential receptor for the neuropeptide of pituitary adenylate cyclase-activating polypeptide (PACAP), which mediates neuroprotective and nerve regenerative activities of PACAP. In this study, we found that in both PAC1R-CHO cells with high expression of PAC1R-eGFP and retinal ganglion cells (RGC-5) with the natural expression of PAC1-R, oligo-peptide PACAP(28-38) and the positively charged arginine-rich penetrating peptide TAT, as positive allosteric modulators of PAC1-R, significantly trigger the nuclear translocation of PAC1-R. The chromatin immunoprecipitation (ChIP)-PCR results show that the nuclear translocated PAC1-R binds with the promoter regions of <italic>PAC1-R</italic> and its specific ligand <italic>PACAP</italic>. The up-regulated promoter activities of <italic>PAC1-R</italic> and <italic>PACAP</italic> induced by PACAP(28-38) or TAT are positively correlative with the increase of the expression levels of PAC1-R and PACAP. Moreover, the nuclear translocation of PAC1-R induced by PACAP(28-38) or TAT is significantly inhibited by the mutation of PAC1-R on Cys25 and the palmitoylation inhibitor 2-bromopalmitate. Meanwhile, the increase in both PAC1-R and PACAP levels and the neuroprotective activities of PACAP(28-38) and TAT in MPP-induced cell model of Parkinson<?A3B2 tf="TT5843c571"?>’s disease are synchronously inhibited by 2-bromopalmitate, which are positively correlated with the nuclear translocation of PAC1-R induced by PACAP(28-38) or TAT. Bioinformatics analysis and motif enrichment analysis following ChIP-sequencing show that the transcription factors including SP1, Zic2, GATA1, REST and YY1 may be recruited by nuclear PAC1-R and involved in regulating the promoter activities of <italic>PAC1-R</italic> and <italic>PACAP</italic>. ChIP-sequencing and related bioinformatics analysis show that the downstream target genes regulated by the nuclear PAC1-R are mostly involved in the process of cellular stress and related to neuroprotection, neuronal genesis and development.
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GeneCards Version 3: the human gene integrator
Marilyn Safran, Irina Dalah, Jake M. Alexander et al. · Database · 2010 · 2.1K citations · Full text
Atsuro Miyata, Lun Jiang, Raymond D. Dahl et al. · Biochemical and Biophysical Research Communications · 1990 · 926 citations