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26 protocols using plx5622

1

Parkin Deletion in Mouse Model

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PLX5622 (batch#98636) was obtained from MedChemExpress LLC (NJ, USA) and incorporated into Teklad 2018SX Grain-based Chow Diet (at 1.2 g/kg PLX5622) by Research Diets Inc (NJ, USA). 6–7-week-old parkinflx/flx mice were administered the PLX5622 diet, or the control Teklad 2018SX Grain-based Chow Diet, (also supplied by Research Diets Inc) for 20 days. Following this, adult-onset DA-neuron specific parkin deletion was accomplished as described in the previous section. Microglia depletion was assessed via immunoblot and IHC analysis for Iba-1.
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2

Microglia Depletion Using CSF1R Inhibitor

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We used PLX-5622, a CSF1R inhibitor, to deplete microglia and reduce peripheral macrophage populations (kindly provided by Plexxikon Inc., Berkley, CA) (Weber et al., 2019 (link)). PLX-5622 was integrated into the diet at a concentration of 1200 mg/kg (Research Diets, New Brunswick, NJ). Mice were started on PLX-5622 or control diet 21 days prior to tumor cell injection and continued on their assigned diets through the duration of the study.
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3

Permanent Distal Middle Cerebral Artery Occlusion in Aged Mice

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C57BL/6J mice of both sexes were used for scRNA-seq at 11–14 weeks or 18–22 months of age. PDMCAO was induced by permanent ligation of the right distal middle cerebral artery (MCA) using a micro-coagulator (Accu-temp)11 (link). Mice were anesthetized with isoflurane (4% induction and 2% maintenance in airflow) and body temperature was maintained at 37°C by feedback-controlled heating pad and rectal temperature probe. Bupivacaine (0.25% at 1ml/kg) was injected subcutaneously (s.c.), prior to any skin incision43 (link). The distal MCA was accessed via a craniotomy and permanently occluded just proximal to the anterior and posterior branches by electrocoagulation. Sham controls were generated with same procedure without electro-coagulation of the MCA.
For microglia depletion experiments, we used PLX5622, a CSF1R antagonist (REF). PLX5622 was provided by Plexxikon Inc. (Berkeley, CA) and formulated in AIN-76A standard chow at 1200 ppm by Research Diets Inc. PLX5622 was administrated for 7 days prior to the PDMCAO procedure and continued for 3 days after stroke. At 3 days after surgery, brains were isolated and ipsilateral hemisphere was used for RNA isolation and qRT-PCR analysis. The contralateral hemisphere was used for immunostaining.
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4

Microglial Depletion Using PLX5622

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Plexxikon Inc. (Berkeley, CA) provided the CSF1R inhibitor PLX5622, which was formulated in AIN-76A chow at a dose of 1200 parts per million by Research Diets (New Brunswick, NJ). Control chow was also provided. Male B6/129SF1 mice (8 weeks old) received either control chow or PLX5622 chow for 7 days before and throughout the withdrawal period. The selected dose and duration of PLX5622 treatment were based on previous studies showing between 80 and 90% microglial depletion with the same dose and treatment duration (65 (link)).
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5

Modulation of Microglial Activation

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Six‐ to eight‐week‐old heterozygous mice were fed with chow containing PLX5622 (1,200 parts per million [ppm] formulated in AIN‐76A standard rodent diet; Research Diets Inc., New Brunswick, NJ) or identical chow without drug for control animals.
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6

Dietary PLX5622 Intervention Study

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Control and PLX5622 (300 ppm formulated in AIN-76A standard chow, Research Diets, Inc.) chows were provided by Plexxikon Inc (Berkeley, CA). Approximately 1.2 mg of PLX5622 was ingested by each mouse per day (calculation based on 4 g/mouse chow daily).
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7

Chow-Based Microglial Depletion Protocol

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The animals received chow containing 1200 mg/kg PLX5622 (Research diets, #113512) 1.5 weeks before the first KXA injection, and were kept on that diet for the whole duration of the experiment (Dagher et al., 2015 ; Spangenberg et al., 2019 ).
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8

PLX5622 Dietary Intervention Protocol

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PLX5622 was provided by Plexxikon Inc. and formulated in AIN‐76A standard chow by Research Diets Inc. PLX5622 was provided ad libitum at 290 mg/kg.
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9

Macrophage Depletion and Repopulation in Mouse Choroid

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We employed a model for macrophage depletion in the adult mouse choroid which involved the dietary administration of PLX5622 (Plexxikon, Berkeley, CA), a potent and selective inhibitor of the CSF1R that we previously demonstrated to deplete microglia in the retina (Zhang et al., 2018 (link)). Animals were placed on a rodent chow containing PLX5622 (at 1200 parts per million, formulated by Research Diets Inc New Brunswick, NJ) for up to 7 weeks to induce depletion macrophages resident in the choroid. To allow for the repopulation of choroidal macrophages, animals subjected to depletion with PLX5622-containing diet for 3 weeks were switched back to a standard diet; the first day of control diet resumption was designated day 0 of the repopulation phase.
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10

Microglia Activation and Cytokine Profiling

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Morphine sulfate was purchased from West-Ward (Eatontown, NJ, USA). PLX5622-containing rodent diet (each kilogram contains 1200 mg PLX5622) was purchased from Research Diets (New Brunswick, NJ, USA). Diphtheria toxin (DT) from Sigma; HibernateA and HibernateA-Ca from BrainBits (Springfield, IL, USA); papain from Worthington Biochemical (Lakewood, NJ, USA); Optiprep Density Gradient Medium from Sigma (St. Louis, MO, USA). Antibodies used for immunoblotting were: anti-IBa1 (1:1000, Wako: 016–20001); anti-GFAP (1:1000, Millipore: MAB360); anti-IL-1β (1:500, Novus Biologicals: NB600–633) and anti-β-actin (1:1000, Santa Cruz Biotechnology: sc-1616-R). The antibody for immunohistochemistry was anti-IBa1 (1:200, Wako: 016–20001). Antibodies used for flow cytometry were: APC-anti-CD11b (Biolegend: 101211), FITC-anti-CD45 (Biolegend: 103107) and anti-CD16/32 (Biolegend: 101302).
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