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Jackson Laboratory sham-operated adx mice
(A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from <t>CD45.2</t> + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
Sham Operated Adx Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory adx and sham-operated mice
(A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from <t>CD45.2</t> + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
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Miltenyi Biotec sham operated mice
(A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from <t>CD45.2</t> + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
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Envigo c57bl/6jolahsd ovariectomized (ovx) and sham operated (sham) female mice
Experimental workflow. Both femurs <t>from</t> <t>C57BL/6JOlaHsd</t> <t>OVX</t> and sham female mice were extracted from each animal; one femur was used for micro-CT measurements and the other for biomechanical testing.
C57bl/6jolahsd Ovariectomized (Ovx) And Sham Operated (Sham) Female Mice, supplied by Envigo, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


(A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from CD45.2 + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).

Journal: bioRxiv

Article Title: Genomic Analysis of Progenitors in Viral Infection Implicates Glucocorticoids as Suppressors of Plasmacytoid Dendritic Cell Generation

doi: 10.1101/2024.10.28.620771

Figure Lengend Snippet: (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from CD45.2 + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).

Article Snippet: C57BL6/J mice, CD45.1 + mice, sham-operated and ADX mice (7-8 weeks old) were purchased from The Jackson Laboratory.

Techniques: Isolation, Infection, Flow Cytometry, Purification, RNA Sequencing Assay

Experimental workflow. Both femurs from C57BL/6JOlaHsd OVX and sham female mice were extracted from each animal; one femur was used for micro-CT measurements and the other for biomechanical testing.

Journal: Scientific Data

Article Title: Murine femur micro-computed tomography and biomechanical datasets for an ovariectomy-induced osteoporosis model

doi: 10.1038/s41597-021-01012-8

Figure Lengend Snippet: Experimental workflow. Both femurs from C57BL/6JOlaHsd OVX and sham female mice were extracted from each animal; one femur was used for micro-CT measurements and the other for biomechanical testing.

Article Snippet: Briefly, C57BL/6JOlaHsd ovariectomized (OVX) and sham operated (sham) female mice at 8-weeks of age were purchased from ENVIGO.

Techniques: Micro-CT