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11 protocols using male dba 1j mice

1

Evaluating Maraviroc Effects on CIA Mice

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Male DBA/1J mice were obtained from Jackson Laboratories (Bar Harbor, ME, USA). All mice were used at 10–12 weeks old and maintained at the College of Pharmacy Animal Facilities of King Saud University. Mice were divided into four groups (n = 6): dimethyl sulfoxide (DMSO) in saline treatment only as the normal control (NC) group, the maraviroc treatment (NC + MVC) group, collagen-induced arthritis (CIA control) group, and CIA + MVC treatment group. All experimental procedures were approved by the Scientific Research Ethical Committee by King Saud University (Ethical Approval No: KSU-SE-19-63).
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2

Pathogen-free DBA1/J Mouse Housing

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Male DBA1/J mice were purchased from Jackson Laboratories (Farmington, CT). Mice were housed under specific pathogen-free conditions and all experiments conducted under a protocol approved by the Mount Sinai Institutional Animal Care and Use Committee.
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3

DBA/1J Mouse Husbandry and Care

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Male DBA/1J mice were purchased at 6 to 8 weeks old from Jackson Laboratory (Bar Harbor, ME, USA) and kept under pathogen-free conditions at an Association and Accreditation of Laboratory Animal Care approved Animal Care Unit at The University of Kansas. All experimental procedures were conducted in accordance with the Guide for the Care and Use of Laboratory Animals as adopted and declared by the U.S. National Institutes of Health, and were conducted under a protocol approved by the Institutional Animal Care and Use Committee at The University of Kansas.
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4

Pathogen-Free Mouse Study Protocol

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Male DBA/1J mice (8-week age) were obtained from The Jackson Laboratory, (Maine, USA), and housed under specific pathogen free conditions with free access to feed and water. The experiments were conducted according to internationally accepted guidelines on the use of laboratory animals and the protocols were approved by the Institutional Animal Care and Use Committee (IACUC) of Daejeon University, Republic of Korea.
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5

Mice Sourcing and Handling for Microbiome Studies

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Male C57BL/6 mice were purchased from Taconic (Rensselaer, NY). Both male and female C57BL/6J, B6.129P2-IL10tm1Cgn/J (IL-10 KO), GFPinducible- C57BL/6-Il17atm1Bcgen/J, male DBA/1J mice, and NOD/ShiLtJ were purchased from Jackson Laboratories (Farmington, CT). Given the C57BL/6 known difference in Th17-inducing intestinal levels of Segmented filamentous bacteria (SFB)22 (link) we tested both Taconic and Jackson mice and they were similarly protected by the high Mg2800 diet in KSIA. Therefore, all the microbiome and FMT experiments used only Taconic mice. KBxN (KRN) TCR transgenic mice (gift from Dr. C. Benoist, Boston, MA) were bred and maintained at Mount Sinai. Mice were housed under specific pathogen-free conditions and all experiments conducted under a protocol approved by the Mount Sinai Institutional Animal Care and Use Committee (protocol number 2014-0283). Mouse experiments were planned according to the ARRIVE guidelines (www.ARRIVEguidelines.org).
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6

Mice Aging and Disease Study

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Male DBA/1J mice (aged 6–8 weeks) were purchased from Jackson Laboratories (Bar Harbor, ME). All studies were reviewed and approved by the Institutional Animal Care and Use Committee at Children’s National Health System.
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7

Housing and Care of DBA/1J Mice

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Male DBA/1 J mice were obtained from the Jackson Laboratory (Bar Harbor, Maine, USA), and were housed in standard laboratory cages and allowed access to tap water ad libitum. The experimental animals were housed in an air-conditioned room at 22–25 °C under a 12 h light–dark cycle. All animals were treated in accordance with the Institutional Animal Care and Use Committee (IACUC) of China Medical University, and the study protocol was approved by the ethics committee of the China Medical University, Taichung, Taiwan.
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8

Housing and Care of DBA/1J Mice

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Male DBA/1J mice were purchased from Jackson Laboratories (Bar Harbor, ME, USA). The mice were housed at 25 ± 2 °C with a 12 h light/dark cycle in a specific pathogen-free environment, fed standard mice chow, and given food and water ad libitum. All experiments were carried out with the approval of the King Saud University Institute's animal use and care committee (KSU-SE-21-64).
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9

Animal Sourcing and Handling for Research

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Female Lewis rats age 6–8 weeks were purchased from Charles River Labs (Portage, MI). NZB/W F1 mice were purchased from Jackson Laboratories (Bar Harbor, ME). C57/BL6 mice were purchased from Taconic Biosciences (Rensselaer, NY). Male DBA1/J mice were purchased from Jackson Laboratories (Bar Harbor, ME). Female Brown Norway rats (12 weeks old) were purchased from Charles River Labs (Wilmington, MA). Balb/CN mice were purchased from Taconic Biosciences (Rensselaer, NY). SJL/J mice were purchased from Jackson Laboratories (Bar Harbor, ME). All animals were acclimated in the facility for at least seven days prior to use with rats were housed three per cage and mice housed five per cage on a 12 ​h light dark cycle with food and water provided ad libitum. All animal studies were performed in accordance with and under protocols approved by the AbbVie Bioresearch Center Institutional Animal Care and Use Committee (IACUC) in accordance with the Principles of Laboratory Animal Care and all applicable national and local laws.
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10

Collagen-Induced Arthritis Mouse Model

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Male DBA/1 J mice (The Jackson Laboratory) were used at 6-8 weeks of age. Mice utilized in these studies were conducted at AbbVie to the standards of the Association for the Assessment and Accreditation of Laboratory Animal Care Standards. All studies with mice were performed according to approved protocols by AbbVie's Institutional Animal Care and Use Committee (IACUC). Arthritis was induced with an intradermal injection at the base of the tail with 100 µl emulsion containing 100 µg type II bovine collagen in 0.1 N acetic acid and 100 µl complete Freund's adjuvant containing 100 µg Mycobacterium tuberculosis H37Ra (BD Difco). A boost of 1.0 mg zymosan A in 200 µl phosphate-buffered saline (Life Technologies, Grand Island, NY) was given 21 days later via an i.p injection. Disease onset occurred within 3-7 days following the boost, and mice were monitored daily for a change in paw swelling with a caliper thickness gauge (Dyer).
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