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Signal Transduction My favorite example… Vibrio fischeri The light organ of the squid contains Vibrio fischeri, which under high cell densities emits luminescence. The signal transduction pathway responsible for turning on the genes responsible for luminescence is called Quorum Sensing. Quorum Sensing in Vibrio fischeri Signaling in prokaryotes: http://wwwuser.gwdg.de/~genmibio/mascher/research1.html Signal Transduction: The process by which a cell responds to an external signal Ligand gated ion channels Calmodulin and calcineurin are examples of calcium binding proteins involved in multiple signaling pathways http://www.answers.com/topic/ligand-gated-ion-channel?cat=technology Transmembrane Receptors >40% of the drugs on the market target specific GPCRs! http://www.sigmaaldrich.com/Area_of_Interest/Life_Science/Cell_Signaling/Scientific_Resources/Pathway_Slides__ _Charts/Diversity_of_G_Protein_Coupled_Receptor_Signal_TDP.html Enzyme-linked Receptors Example: Insulin receptor http://www.uic.edu/classes/bios/bios100/mike/spring2003/lect07.htm MAPKKK MAPKK MAPK http://www.uic.edu/classes/bios/bios100/mike/spring2003/lect07.htm Unicellular eukaryotes are much more complex Signaling pathways can overlap! Klipp et al. BMC Neuroscience 2006 7(Suppl 1):S10 doi:10.1186/1471-2202-7-S1-S10 Multicellular eukaryotes have very complex signaling pathways! Nuclear Factor of Activated T cells (NF-AT) http://www.ambion.com/tools/pathway/pathway.php?pathway= Activation%20of%20cAMP-Dependent%20PKA B3Z Helper T cells stimulate B cell antibody production as well as activate other T cells http://www.unis.org/UNIScienceNet/Heart&CVS_knowledge.html IL-2 production requires activation of NF-AT IL-2 binds to IL-2 receptor on T cells and stimulates T cell proliferation Helper T cells recognize antigens presented by an antigen-presenting cell in combination with Class II major histocompatibility complex (MHC) http://www.blobs.org/science/article.php?article=12 Crabtree, 1999 Phospholipase C is activated by T cell receptor activation also The drop in ER Ca2+ stimulated Ca2+ entry into the cell via CRAC http://www.rsc.org/delivery/_ArticleLinking/ArticleLinking.asp?JournalCode=NP&Year=2007&ManuscriptID=b407701f&Iss=4 Crabtree, 1999 IL-2 Gene mRNA START -286 -257 -256 -242 -208 -188 -158 -145 -93 -66 +1 TATA NF-AT NFIL-2D (OCT?) NFIL-2C (NF-KB) NFIL-2B ATG +48 NFIL-2A (OCT?) DNA Binding Proteins NFAT Z Construct -70 +1 +47 TATA TK Promoter Hygromycin resistance gene NF-AT NF-AT NF-AT Trimer of the NF-AT Binding Site IL-2 Your B3Z cells have been transfected with the lacZ reporter ATG lacZ The reporter we are using only has the lacZ gene from this operon http://fig.cox.miami.edu/~cmallery/150/gene/operon.htm http://www.answers.com/topic/beta-galactosidase?cat=technology X-gal Blue Yellow We will be using chlorophenol red galactoside (CPRG) (Turns from yellow to purple in the presence of -galactosidase) Activators and inhibitors you will be using…. ConA: T cell activator; crosslinks cell surface receptors EGTA: T cell inhibitor; chelates Ca2+ Cyclosporin (CsA): T cell inhibitor; binds and inhibits the cyclophilin receptor Rapamycin: Neither a T cell activator or inhibitor; inhibits phosphorylation and activation of p70 S6 kinase Ionomycin: T cell inhibitor; a Ca2+ ionophore PMA: T cell activator; specifically activates the PKC pathway Day 1: •Data presentations and journal club •Watch video •Count cells using a hemacytometer •Subculture B3Z cells for next lab class Goal: To avoid contamination… 70% Ethanol Laminar Flow Hood Must practice exceptional aseptic technique!!!! •Wash hands/gloves before beginning •Wipe area before/after work and if spills occurring during work with 70% ethanol •Work quickly to minimize exposure T-flask Most cell types B3Z cells •Mammalian cells normally grow as a single layer and can be disrupted for subculturing by treatment with proteolytic enzymes •Growth conditions are 37°C with 5% CO2 and require a “CO2 incubator” •Cells are usually grown until confluency is reached •You will be using T cells called “B3Z” which have little to no attachment to flask surface and thus do not need to be treated with proteolytic enzymes Hemacytometer: Use 10X objective 1 2 5 3 4 Count the number of cells in squares 1-4; determine average # cells/square Average # cells/square X 104 = # cells/ml Day 2: •Harvest cells •Treat with activators/inhibitors •Harvest cells •Perform -galactosidase assay •The plates will be read for you but make sure to get the data so that you can do the calculations Notebooks are due at the BEGINNING of the last class-This is Wed Dec 5th for the M/W section and Thurs Dec 6th for the T/Th section