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Image Search Results
Journal: Developmental cell
Article Title: Fate mapping in mouse demonstrates early secretory differentiation directly from Lgr5+ intestinal stem cells.
doi: 10.1016/j.devcel.2024.12.023
Figure Lengend Snippet: Figure 2. Two distinct types of behavior in the crypt (A) Schematics of Lrig1;mTmG fate mapping experiment. Tissue was collected 48, 72, and 96 h post labeling (4-OHT injection). (B) Representative images of top- and bottom-rooted Lrig1 clones at 48, 72, and 96 h. mG (green) and non-clone cells, mT (magenta), and DAPI (blue). Scale bar, 20 mm. (C and D) Lrig1 clone sizes over time, separated by position (top or bottom rooted). Points represent individual clones. Number of clones is shown below x axis, and boxplots indicating the lower and upper quartiles as well as medians. Statistical significance was tested with non-paired Mann-Whitney (p < 0.0001). (E) Schematics of EdU/BrdU double labeling experiment. (F) Representative images of crypts (top and bottom), 15 h after the EdU pulse. EdU (magenta), BrdU (yellow), DAPI (blue), and E-cadherin (green). Scale bar, 10 mm. (G) EdU+BrdU+ over EdU+ cells in bottom and top compartment. Point represents individual mice (averaged over four crypts). Plot shows means ± SD. (H) Schematic of the mathematical model. (I) Mean Lrig1 clone sizes of top- (red) and bottom-rooted (blue) clones. Lines show model predictions, and shaded areas indicate 95% confidence intervals. Experimental data are means ± SD. Model parameters are listed in Table S2.
Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Rabbit Polyclonal anti Human Lysozyme EC 3.2.1.17 (Concentrate) Agilent Dako Cat #: A0099; RRID: AB_2341230 Mouse Monoclonal anti
Techniques: Labeling, Injection, Clone Assay, MANN-WHITNEY