In Vitro Gene expression analysis assays are essential for understanding how up or down regulation of related target proteins could result in pathologies. Dorsal Root Ganglion (DRG), Neuronal and Glial Cultures have proven hard to transfect as as many transfection reagents are toxic to these cells. It is important for the study of neuro-diseases that researchers have tools and methods that enable success.
In this study, researchers successfully transfect DRG cultures with IKAP-shRNA using our pn-Fect kit. The own regulation of IKAP in these cultures support findings that helped explain the potential pathology of Familial Dysautonomia (FD; Hereditary Sensory Autonomic Neuropathy; HSAN III): Hunnicutt BJ , Chaverra M , George L , Lefcort F , 2012 IKAP/Elp1 Is Required In Vivo for Neurogenesis and Neuronal Survival, but Not for Neural Crest Migration. PLoS ONE 7(2): e32050. doi:10.1371/journal.pone.0032050.
Cell culture: Dorsal root ganglia
were dissected from Embryonic day 5–9.5 chick embryos (E5–9.5) and dissociated
by incubation in 0.25% trypsin-EDTA (Gibco) for 7 min at 37 C followed by
trituration through fire–pulled glass pipettes. The culture media consisted of
Neurobasal medium (Invitrogen) supplemented with B27 (1X,Invitrogen), Glutamax
(1X,Invitrogen), Hybrimax Antibiotic\Antimicotic (1:100, Sigma), NGF (10 ng/ml,
gift from Dr. Thomas Large). Cells were plated on 8-well Nunc glass chamber
slides that were coated with poly-D-lysine (1:100, Sigma) and laminin 20 ug/ml
(Gibco). Approximately equal numbers of cells (52,500) were plated per well.
Immediately after plating, cells were transfected with IKBKAP-7.4 shRNA or
control shRNA via pn-Fect (Neuromics, PN3375). Several ratios of pnfect:DNA were
tested with the optimum obtained 1.84:1. The cells were then cultured for
approximately 29 h at 37 C, 5.5% C02. After incubation culture cells were fixed
and inmunostained as previously described . To determine whether IKBKAP shRNAs
altered cell proliferation and/or neuronal differentiation in dissociated DRG
cultures, Brdu was added to the cultures and the cells were fixed 24 hrs later
(as described in ). The number of
GFP+/BrdU+ or GFP+/Tuj-1+ cells were quantified for each experiment, and a ratio
comparing control vs. IKBKAP shRNAs for each experiment determined. For the
BrdU+ experiment, a total of 556 GFP+/control shRNA transfected cells were
counted and 357 GFP+/IKBKAP shRNA transfected cells in 3 separate experiment.
For determining neuronal differentiation, a total of 2866 GFP+/control shRNA
transfected cells and 2913 IKBKAP shRNA transfected cells were counted, over 3
Images: IKAP regulates neuronal differentiation in the DRG. Reduction in IKAP leads to increased numbers of neurons in the immature DRG (A–C). Embryos at St. 12 were transfected with either control shRNAs or IKBKAP shRNAs and analyzed at St 24/25. Embryos were sectioned, and immunolabled with the neuronal markers Tuj-1 or Ben and the percentage of GFP+ neurons determined. Significantly more IKBKAP shRNA transfected DRG precursor cells differentiated into neurons (arrows in B; IKBKAP shRNA 7.4; n = 3 embryos; p = 0.002; IKBKAP shRNA 1.6 & 4.5, n = 3 embryos; p = 0.001) than Control shRNA transfected DRG precursor cells (n = 5 embryos). (D–H) IKBKAP shRNA-transfected DRG precursor cells (n = 3 embryos; 252 cleaved-Caspase 3+ cells counted) were also more likely to die by apoptosis (compare D & E to F & G) than control shRNA-electroporated cells (n = 3 embryos; 117 cleaved caspase-3+ cells counted). (H) The number of cleaved Caspase 3+ cells was quantified in DRG on both the transfected side of the embryo and the non-transfected side of the embryo and a ratio determined. Significantly more cleaved-Caspase 3+ cells were present in the transfected DRG of IKBKAP shRNA transfected embryos than in the transfected DRG in embryos transfected with control shRNAs; p = 0.006. (I–N). Over-expression of the c-terminus of IKAP prevents neural crest cells from coalescing with the DRG (I, K, L; p = 0.004) but the few that do join, tend not to differentiate into neurons (p = 0.007; J, M, N). Embryos were transfected with either a construct driving expression of the c-terminus of chicken IKAP with a His tag (CT-IKAP-His; L,N) or a control, His-tagged construct (K, M) and analyzed at St. 21. The location and neuronal identity of transfected cells was determined in 3 embryos for each treatment; Control His-plasmid: n = 343 transfected cells counted; CT-IKAP-His: n = 278 transfected cells counted. Statistical analysis by Student t-test. doi:10.1371/journal.pone.0032050.g006.
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