As in our Toll-like Receptor (TLR) signaling screen, stimulated ex vivo thioglycolate-elicited peritoneal cells are used to discover components involved in sensing cytoplasmic double-stranded DNA (dsDNA).  While a non-redundant cytoplasmic sensor remains to be found, dsDNA is known to induce production of type I interferon through a TANK-binding kinase 1 (TBK1)-, inhibitor of NF-κB kinase ε (IKKε)-, and interferon regulatory factor 3 (IRF3)-dependent pathway (1;2).  This occurs independently of TLR signaling.  The dsDNA macrophage screen is designed to probe for additional components of this pathway by isolating macrophages from N-ethyl-N-nitrosourea (ENU)-mutagenized mice, stimulating them with dsDNA and assaying the production of type I interferon.

1. Three to four days prior to PEC isolation, 5mL syringes filled with Brewer’s thioglycolate medium are used to inject mice intraperitoneally with 1.5-2mL through a 25-gauge needle.
2. Immediately prior to isolation, mice are anaesthetized under isofluorane vapour (2-5% v/v, 2% O₂).
3. 5mL syringes filled with sterile PBS are used to recover PECs by lavage through an 18-gauge needle. Once obtained, exudate is added to 5mL of PEC recovery solution in a 15mL conical tube, and stored on ice.
4. Tubes containing exudate are centrifuged for 5 minutes at 1500 rpm in a tabletop centrifuge, and supernatant is replaced with 1mL of PEC medium. Pelleted cells are resuspended by pipeting, and a 20μL aliquot is taken for cell enumeration.
5. The concentration of each cell sample is adjusted to 1x10⁶ cells/mL using PEC medium, and 50μL of each sample (5x10⁴ cells) is added to duplicate columns of a tissue culture-treated 96 well flat-bottomed plate, leaving two columns (11 & 12) unoccupied per plate (Table 2). Plates are incubated at 37^oC/5%CO₂ in a humidified incubator for at least 30 minutes to allow cells to adhere to the plate.

1. Following preincubation of PECs in the 96 well plate, non-adherent PECs are discarded along with residual medium, and 100μL of OptiMEM is added to all wells apart from those in columns 11 & 12. Plates are incubated at 37^oC/5%CO₂.
2. 0.1μg dsDNA is mixed with 25μL OptiMEM medium per well to be assayed (11.5uL dsDNA in 2875μL OptiMEM/plate) and mixed gently.
3. 0.25μL Lipofectamine 2000 is mixed with 25μL OptiMEM medium per sample to be assayed (28.75μL Lipofectamine in 2875μL OptiMEM/plate), mixed gently and incubated at room temperature for five minutes.
4. Lipofectamine and dsDNA solutions are gently mixed in one tube, and incubated at room temperature for twenty minutes.
5. 50μL of Lipofectamine/dsDNA mix is added to all sample wells of the 96 well plate, and plates are incubated overnight for ~16 hours.
6. Following incubation, supernatant is transferred into a new 96 well plate until used in the type 1 interferon bioassay (3b), and replaced with 100μL/well of MTT solution in PEC medium, and incubated overnight at 37^oC/5%CO₂.

1. On the day prior to bioassay, 5x10⁴ L-929-ISRE cells are added to every well of a white, tissue culture-treated 96 well flat-bottomed plate in a volume of 100μL L-929 medium, and incubated overnight at 37^oC/5%CO₂.
2. A mouse recombinant IFNβ standard series is prepared immediately prior to bioassay, using 7 serial two-fold dilutions (starting from ~100U/mL) and L-929 medium alone. 100μL of each standard point is added in duplicate to columns 11 & 12 of each L-929-ISRE plate (organized as in Table 1),
3. Immediately prior to bioassay, the supernatant of L-929-ISRE cells is discarded and replaced with 75μL of PEC-conditioned media, and incubated at 37^oC/5%CO₂ for 6-8 hours.
4. Following incubation, supernatant is discarded and plates are washed once with 200μL/well PBS.
5. PBS is then discarded, and 30μL/well reporter lysis buffer is added.
6. Plates are incubated at -70^oC for greater than one hour.
7. After plates have thawed, 50μL/well of Luciferase Assay System solution is added, and luminescence read immediately.

Bioactive type 1 IFN concentrations are inferred from the standard curve of [IFNβ] versus ISRE-dependent luminescence.  For PEC plates, the absorbance values provide an indication of the number of live cells used in the IFN bioassay.  To adjust for sample to sample variation in PEC number (which may affect the amount of IFN produced), the calculated IFN concentrations must be normalized.  Average absorbance of each PEC sample (e.g. average absorbance of columns 1 and 2, 3 and 4, 5 and 6, etc. on PEC plate) is divided by the total average absorbance across all PEC plates.  The resulting figure is used to normalize each IFN concentration value.  Typically, samples falling outside three standard deviations of the mean are considered putative mutants, and leftover PEC solution may be used for ligand dose-response retesting.