mplify the nomenclature we named the recombinant Vero-cells adapted rgA75/17-V as ��CDV”. Construction of expression plasmids: The plasmids pF-CDV, pF-CDV-ER, pH-CDV and pN-CDV were described previously. After expression, the CDV proteins are named F CDV, FER CDV, H CDV and N CDV proteins, respectively. The constructs were made in the mammalian expression vector pCI using PCR and recombinant PCR techniques. All plasmid sequences were confirmed by automated nucleotide sequence analysis. Cell culture, infection, and transfection Vero cells were grown in Dulbecco’s modified Eagle’s medium supplemented with 10% fetal calf serum, penicillin, and streptomycin and all the cultures were incubated at 37uC in a humidified atmosphere containing 5% CO2, as previously described. Hippocampal rat brain cells were prepared from new born rats and were approved by the cantonal regulation of animal care. Hippocampi without dentate gyri were dissociated with papain and triturated using a glass pipette. After centrifugation at 400 g for 2 minutes, cells were plated on individual wells of 6well plates, each containing poly-D-lysin/laminin-coated borosilicate BMS-345541 coverslips at a density of 250000 cells/dish Calcium signal analyses To follow Ca2+ signals, GFP-aequorin was used. GA is a fusion protein between aequorin and GFP, which emits luminescent signals when it binds 3 Ca2+ ions. This requires the presence of coelenterazine for the intracellular regeneration of the photoprotein. When Ca2+ binds to the aequorin protein, it CDV Glycoproteins 
Induce Vasostatin Release undergoes a conformation change that results in the oxidation of coelenterazine and the emission of a single photon. In the jellyfish, binding of Ca2+ to aequorin results in an intermolecular nonradiative energy transfer to GFP. This process is known as chemiluminescence resonance energy transfer. In our case, GFP and aequorin were fused genetically and an intramolecular transfer of Ca2+ activated aequorin luminescence energy to GFP occurred, resulting in the emission of a green light. GA is therefore a bi-functional reporter, whereby expression patterns can be monitored by GFP fluorescence, while Ca2+ activities can be measured by GFP fluorescence with singlecell resolution. GA expression was obtained via transfection of the corresponding recombinant plasmid. Coelenterazine is PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22189475 membrane permeable and was added to the transfected cells at 5 mM, for pre-incubation at 37uC for 60 min in a tyrode buffer containing Ca2+. In Vero cells, Ca2+ signals were then recorded in phenol red-free DMEM, L-glutamine, FCS 10%, Hepes medium while hippocampal rat brain cells were recorded in a medium containing NaCl, KCl, CaCl2, glucose, Hepes, MgCl2, pH 7,4. The calibration of photon data was carried out as follows. Light emission is expressed as the fractional rate of photoprotein consumption, which is the ratio between the emission of Light from that time point and the integral of total light emission from that point until full exhaustion of the photoprotein. Photons were counted over 60 seconds every 10 minutes during 24 hours, by using a photon counting system. After 17 hours of recording in Vero cell cultures, or 21 hours for the hippocampal rat brain cells, ionomycin was added to release all Ca2+ from ER stores and from the cells. A high CaCl2 solution was then added in order to quantify the total amount of photoprotein. Each sample was analysed in triplicate in three separate experiments. Quantification of viral
