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Ai9 reporter mice

Manufactured by Jackson ImmunoResearch
Sourced in United States

The Ai9 reporter mice are a genetic model designed to express the tdTomato fluorescent protein in a Cre-dependent manner. This allows for the visualization and tracking of Cre-expressing cells and their lineage.

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9 protocols using ai9 reporter mice

1

Transgenic Mouse Models for Fracture Healing

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All of the animal procedures were approved by the UConn Health Institutional Animal Care and Use Committee, and experiments were performed in accordance with its guidelines and regulations, and authors complied with the ARRIVE guidelines. We used αSMACreERT2 and Col2.3GFP mice that have been previously described in refs. 4 (link),44 (link). Ai9 reporter mice (007909), were purchased from Jackson Labs45 (link). We backcrossed PDGFRβfl/fl (129S4/SvJaeSor) generated by Dr. Phillipe Soriano46 (link) for 8 generations to C57Bl/6J background. All strains were maintained on a C57Bl/6J background. Mice were housed in ventilated cages, maintained at 22 ± 2 °C, 55 ± 5% humidity, and 12-h light/dark cycle with ad libitum access to food and water. αSMACreERT2 mice were crossed with the Ai9 reporter mice (Jackson Labs) and Col2.3GFP mice, and triple transgenic male mice αSMACreERT2/Ai9/Col2.3GFP (termed SMA9/Col2.3GFP) were used at the age of 5–7 months for evaluation of growth factor efficiency. For fracture healing, αSMACreERT2/PDGFRβfl/fl Cre+ experimental animals and Cre littermates as controls at 8–10 weeks of age, were treated with tamoxifen (75 µg/g). We determined genotype for Cre, Pdgfrβ and DNA recombination by PCR (primer sequences in Supplementary Table 1).
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2

Modeling Osteogenesis Imperfecta in Mice

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All animal procedures were approved by an institutional animal care committee. To model osteogenesis imperfecta, oim on a C57Bl/6 background (obtained from Dr. Charlotte Philips, Univ. of Missouri) that lack functional Col1a2 were utilized [27 (link)]. OIM homozygous mice were used for all experiments. OIM mice were genotyped as previously described [28 (link)]. Donor cells were sourced from mice that are a combination of the three previously described lines: αSMACreERT2 [24 (link)], Col2.3GFP [26 (link)] and Ai9 reporter mice (stock # 007909, Jackson Laboratory) [29 (link)]. To generate αSMACreERT2/Ai9/Col2.3GFP mice, αSMACreERT2/Col2.3GFP were bred with Ai9, and termed SMA9/Col2.3GFP. To assess recombination efficiency αSMAGFP mice were crossed with αSMACreERT2/Ai9 [30 (link)].
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3

Rodent Neurobiology Procedures and Ethics

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Six weeks old male Sprague–Dawley rats weighing 167.8 ± 7.3 g (purchased from the Experimental Animal Center of the Fourth Military Medical University, Xi'an, Shaanxi, China) were used in the behavioral, immunohistochemistry, western blot, and ELISA experiments. Adult heterozygous male vGlut2-Cre mice (Jackson Laboratories) were crossed with Ai9 reporter mice (Jackson Laboratories) to generate vGlut2-tdTomato mice. Young adult (3–5 weeks old) male vGlut2-tdTomato mice were used for electrophysiological experiments. Animals were group-housed (4 per cage) at a temperature of 22-24°C, with a 12-hour light/dark cycle and free access to food and water. All rats were acclimatized to the laboratory conditions for at least 7 days before experimental manipulation in case their stress responses affected the experiment results. All animal experiments were approved by the Ethic Committee of the Fourth Military Medical University and followed the policies for the use of laboratory animals issued by the International Association for the Study of Pain. All efforts were made to minimize the number of animals used and their suffering.
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4

Derivation of Transgenic Mouse ESCs

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Hcn4-GFP, Tbx1C, Ai9 mice were obtained by crossing Hcn4-GFP mice32 (link) with Tbx1-Cre mice17 (link) and Ai9 reporter mice (stock no. 007909, Jackson Laboratory). The appearance of the vaginal plug was considered as day 0.5 of gestation (E0.5). Mouse ESCsHcn4-GFP; Tbx1-Cre; Ai9 were derived from blastocysts (E3.5) harboring Hcn4-GFP; Tbx1-Cre; Ai9 and mESCIsl1-Cre, α MHC-GFP -GFP; Ai9 were derived from blastocysts (E3.5) harboring Isl1-Cre36 (link), αMHC-GFP47 (link); Ai9. All animals were housed at the Johns Hopkins Medical Institutions. All protocols involving animals followed U.S. NIH guidelines and were approved by the animal and care use committee of the Johns Hopkins Medical Institutions.
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5

Notch1 Signaling Overexpression in Mice

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All animal procedures were approved by an UConn Helth Institutional Animal Care and Use Committee prior to performing the study. Mice were housed in ventilated cages maintained at 22 ± 2°C, 55 ± 5% humidity, and 12-hour light/dark cycle. To generate mice overexpressing NICD1 we used αSMACreERT2 mice 18 (link) and bred them with previously described Gt(ROSA)26Sortm1(Notch1)Dam/J (termed RosaNICD1) mice obtained from Jackson labs # 008159 19 (link) to generate αSMACreNICD1. Cre littermates were used as controls. For the lineage tracing experiments we crossed αSMACreNICD1 mice with the Ai9 reporter mice (Jackson labs, stock # 007909) to generate αSMA9/NICD1. We determined genotype for Cre, NICD and DNA recombination by PCR (Supplemental table 1)8 (link). To study the effect of Notch1 signaling inhibition αSMA9 mice were used.5 ; 20 (link) We utilized males and female mice on a C57Bl/6J background.
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6

Conditional Inactivation of IRβ in Tendons

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To drive loss of IRβ in the tendon, IRβflox/flox (#6955, Jackson Laboratories)29 (link), were crossed to S100a4-Cre mice (#12641, Jackson Laboratories), resulting in IRcKOS100a4 mice. Cre-; IRβflox/flox littermates were used as wild type (WT) controls. To confirm efficient targeting of the tendon, S100a4-Cre mice were crossed to Ai9 reporter mice (#7909, Jackson Laboratories)30 (link), resulting in tdTomato fluorescence upon Cre-mediated recombination. Mice were sacrificed at 48 weeks of age.
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7

Murine Genetic Models for Cell Lineage

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All work was performed as approved by the animal use and care committee at Washington University (St. Louis, MO, USA). Mice were housed on a 12‐hour light/dark cycle and fed ad libitum (PicoLab 5053, LabDiet, St. Louis, MO, USA). C57BL6J (JAX Strain #000664), C3H/HeJ (JAX Strain #000659), Baf53b‐Cre (JAX Strain #027826), and Ai9 reporter mice (JAX Strain #007909) were obtained from Jackson Laboratories (Bar Harbor, ME, USA). Schwann cell reporter mice were a kind gift of Dr Jeffrey Milbrandt and were generated by crossing the following strains: P0‐Cre (JAX Strain 017927)(24) and Ai9‐flox/flox (JAX Strain 007909).(25)
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8

Mice Husbandry and Genotyping Protocol

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All experiments using mice followed NIH guidelines and were approved by the National Institute of Dental and Craniofacial Research ACUC. Mice were housed in small social groups (4-5 animals) in individually ventilated cages under 12-hour light/dark cycles and fed ad libitum. Animals of both sexes aged 7-12 weeks were used in experiments. C57Bl/6N wild-type mice were purchased from Envigo (Indianapolis, IN). TH-IRES-CreER mice (The Jackson Laboratory, stock #00852), TH-IRES-Cre mice (European Mouse Mutant Archive; stock #: EM:00254; backcrossed 5 generations with C57Bl/6NJ mice) and Ai9 reporter mice (The Jackson Laboratory, stock #007909) were bred in house. Animals were randomly allocated to the different experimental conditions reported in this study. Genotyping of offspring from all breeding steps was performed with genomic DNA isolated from tail snips.
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9

Transgenic Mouse Breeding Protocol

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A total of 138 mice were used in these experiments. All experiments were approved by the Pennsylvania State University Institutional Animal Care and Use Committee. Adult (over 8 weeks of age) male and female C57BL/6 J (stock #000664, The Jackson Laboratory), hemizygous SST-IRES-Cre mice (stock #013044, The Jackson Laboratory) and Ai9 reporter mice (stock #007909, The Jackson Laboratory) on C57BL6/J background were bred in-house and genotyped by standard PCR protocol (additional detail available in supplemental methods).
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