And its signalling partners are also expressed by mature T cells [19], thus, lineage targeted strategies will be critical to elucidate the contribution of RET signals to T cell function.Materials and Methods MiceC57Bl/6J (CD45.2, CD45.1 and CD45.1/CD45.2), Rag12/2 (CD45.2 and CD45.1) [35], CD2Cre [23], Gfra12/2 [20], Gfra22/ 2 [21], Ret2/2 [22], and RetMEN2B [24] all in C57Bl/6J background, were bred and maintained at the IMM animal facility. All animal procedures were performed in accordance to national guidelines from the Direcao Geral de Veterinaria (permit ?number 420000000/2008) and approved by the committee on the ethics of animal experiments of the Instituto de Medicina Molecular.Generation of Ret conditional knockout miceTo generate mice LED-209 harbouring a conditional Ret knock-out allele we engineered a targeting construct that firstly, included the introduction of a floxed 2.1 kb, Neomycin resistance (Neor) cassette under the control of the phosphoglycerate kinase-1 (PGK) promoter and a polyA tail (pA). This cassette (PGK-RET Signalling and T Cell DevelopmentNEOr-pA) was inserted approximately 4.5 kb upstream at the Xho I site of the pBluescript KS (pBS KS) vector that carried approximately 13 kb of the 59 end of mouse Ret genomic locus flanking exon 1. The second modification included an insertion of a loxP ,2.5 kb downstream of exon 1, at the Hind III site in the intron between exons 1 and 2 of the mouse Ret locus. Finally, a viral thymidine kinase cassette (,3 kb) under the control of the PGK promoter (PGK-TK-pA) was inserted at the Hind III site ,5 kb downstream of the inserted LoxP site. To obtain homologous recombination, this targeting construct was linearised by Xho I, purified by gel elution and extraction using the Qiaquick gel extraction kit (Qiagen), prior to electroporation into 129SvJderived R1 ES cells grown on mouse embryonic fibroblast (MEF) feeder layers. Following double selection with 300 mg/ml Geneticin (G418, Invitrogen) and 2 mM Gancyclovir (Sigma), positive clones were identified by Southern blotting. Genomic DNA was digested with Hind III restriction enzymes and a 59 external probe of 500 bp was used to screen for positive clones. With the Hind III digest the WT and mutant alleles showed a band size of 16.5 kb and 6 kb respectively. Positive animals were subsequently crossed with transgenic mice expressing Vav1-iCre [23] in order to delete the PGK-NEOr-pA cassette. This MedChemExpress 298690-60-5 recombination resulted in generating the floxed Ret mice wherein the two remaining LoxP sites were found flanking the first exon of the Ret locus, or the complete deletion of the first exon. These mice are further designated as Ret floxed (Retfl) and Ret null (Retnull). Mice were further screened by PCR. Primer sequences were: P1: AAG CTC CCT CCT ACC GTG CT; P2: TGG GAT GAA 1527786 CTC TGC CCA TT; P3: TGC TGC TCC ATA CAG ACA CA; P4: TAC ATG CTG TCT GCT CTC AG.Man Gene Expression Master Mix (Applied Biosystems) was used in real-time quantitative PCR. TaqMan Gene Expression Assays bought from Applied Biosystems were: Gapdh Mm99999915_g1; Hprt1 Mm00446968_m1; Nrtn Mm03024002_m1; Gdnf Mm00599849_m1; Ret Mm00436304_m1.Competitive reconstitution chimerasFoetal livers from C57Bl/6 (CD45.1/CD45.2), CD2Cre/Retnull/fl (CD45.2, conditional knockouts) or CD2Cre/RetWT/fl (CD45.2, controls) were made into single cell suspensions and enriched for precursors by staining with anti-CD117-APC followed by magnetic cell sorting with anti- APC microbeads (Miltenyi Biotec.And its signalling partners are also expressed by mature T cells [19], thus, lineage targeted strategies will be critical to elucidate the contribution of RET signals to T cell function.Materials and Methods MiceC57Bl/6J (CD45.2, CD45.1 and CD45.1/CD45.2), Rag12/2 (CD45.2 and CD45.1) [35], CD2Cre [23], Gfra12/2 [20], Gfra22/ 2 [21], Ret2/2 [22], and RetMEN2B [24] all in C57Bl/6J background, were bred and maintained at the IMM animal facility. All animal procedures were performed in accordance to national guidelines from the Direcao Geral de Veterinaria (permit ?number 420000000/2008) and approved by the committee on the ethics of animal experiments of the Instituto de Medicina Molecular.Generation of Ret conditional knockout miceTo generate mice harbouring a conditional Ret knock-out allele we engineered a targeting construct that firstly, included the introduction of a floxed 2.1 kb, Neomycin resistance (Neor) cassette under the control of the phosphoglycerate kinase-1 (PGK) promoter and a polyA tail (pA). This cassette (PGK-RET Signalling and T Cell DevelopmentNEOr-pA) was inserted approximately 4.5 kb upstream at the Xho I site of the pBluescript KS (pBS KS) vector that carried approximately 13 kb of the 59 end of mouse Ret genomic locus flanking exon 1. The second modification included an insertion of a loxP ,2.5 kb downstream of exon 1, at the Hind III site in the intron between exons 1 and 2 of the mouse Ret locus. Finally, a viral thymidine kinase cassette (,3 kb) under the control of the PGK promoter (PGK-TK-pA) was inserted at the Hind III site ,5 kb downstream of the inserted LoxP site. To obtain homologous recombination, this targeting construct was linearised by Xho I, purified by gel elution and extraction using the Qiaquick gel extraction kit (Qiagen), prior to electroporation into 129SvJderived R1 ES cells grown on mouse embryonic fibroblast (MEF) feeder layers. Following double selection with 300 mg/ml Geneticin (G418, Invitrogen) and 2 mM Gancyclovir (Sigma), positive clones were identified by Southern blotting. Genomic DNA was digested with Hind III restriction enzymes and a 59 external probe of 500 bp was used to screen for positive clones. With the Hind III digest the WT and mutant alleles showed a band size of 16.5 kb and 6 kb respectively. Positive animals were subsequently crossed with transgenic mice expressing Vav1-iCre [23] in order to delete the PGK-NEOr-pA cassette. This recombination resulted in generating the floxed Ret mice wherein the two remaining LoxP sites were found flanking the first exon of the Ret locus, or the complete deletion of the first exon. These mice are further designated as Ret floxed (Retfl) and Ret null (Retnull). Mice were further screened by PCR. Primer sequences were: P1: AAG CTC CCT CCT ACC GTG CT; P2: TGG GAT GAA 1527786 CTC TGC CCA TT; P3: TGC TGC TCC ATA CAG ACA CA; P4: TAC ATG CTG TCT GCT CTC AG.Man Gene Expression Master Mix (Applied Biosystems) was used in real-time quantitative PCR. TaqMan Gene Expression Assays bought from Applied Biosystems were: Gapdh Mm99999915_g1; Hprt1 Mm00446968_m1; Nrtn Mm03024002_m1; Gdnf Mm00599849_m1; Ret Mm00436304_m1.Competitive reconstitution chimerasFoetal livers from C57Bl/6 (CD45.1/CD45.2), CD2Cre/Retnull/fl (CD45.2, conditional knockouts) or CD2Cre/RetWT/fl (CD45.2, controls) were made into single cell suspensions and enriched for precursors by staining with anti-CD117-APC followed by magnetic cell sorting with anti- APC microbeads (Miltenyi Biotec.
