Nces) equipped with FlowJo software (Tree Star Inc. Ashland, OR). The

Nces) equipped with FlowJo software (Tree Star Inc. Ashland, OR). The gating profiles and trees are shown in Fig. S1A and B, and were generated according to [19].`Cell and Tissue Preparation for Western Blot AnalysisCells were rinsed with PBS and scraped into a high salt lysate buffer (25 mM HEPES pH 7.4, 300 mM NaCl, 1.5 mM MgCl2, 1 mM EGTA, and 0.5 Triton X100, with Halt protease and 370-86-5 phosphatase inhibitor cocktails, Pierce, Rockford, IL). For tissues, mammary glands were snap frozen in liquid nitrogen and ground with a mortar and pestle. The resulting powder was mixed with high salt buffer containing protease and phosphatase inhibitors and homogenized for ten seconds, twice, at 4uC with a Polytron (Kinematica, AG, Switzerland). The resulting tissue and cell lysates were cleared for 20 min at 10 000 g at 4uC and the supernatant was analyzed by Western blotting. Antibodies used as probes were: anti-phospho-Lrp6 (detecting both phospho-Lrp6 and phospho-Lrp5; Cell Signaling Technology), anti-vinculin (Millipore), and anti-b-actin (clone AC-15, Sigma-Aldrich). Secondary antibodies were peroxidase-conjugated anti-mouse IgG (Jackson ImmunoResearch Laboratories, West Grove, PA) and horseradish peroxidase conjugated anti-rabbit IgG (InVitrogen).Whole Mount Staining and ImmunohistochemistryMammary glands were fixed and processed to visualize ductal trees as described [17]. General methods for immunohistochemical analysis of paraffin-embedded mammary samples include antigen retrieval as described [17]. Primary antibodies are: antiKi67 (BD Biosciences, Franklin Lakes, NJ), Keratin 5 Clone AF 138 (Covance, Emeryville, CA), Keratin 8 (The University of Iowa ?Developmental Studies Hybridoma Bank, Iowa City, Iowa), cH2AX (Millipore, Billerica, MN), BrdU (Roche, Indianapolis, IN), phospho-Ser15 p53 (Cell Signaling Technology, Beverly, MA). Secondary antibodies and reagents were: AlexaFluor 488 goat anti-mouse, AlexaFluor 546 goat anti-rat, AlexaFluor 488 goat anti-rabbit, AlexaFluor 647 goat anti-rabbit, Pacific Blue conjugated goat anti-rabbit (all from Invitrogen, DprE1-IN-2 web Carlsbad, CA). To calculate the mitotic index of basal and luminal cells, paraffin sections of mammary glands from BrdU-injected mice were counterstained with lineage-specific markers (K5 and K8), together with a nuclear stain (to score the total cell number of each cell type). To describe the focalized nature of the excess mitotic index in genotoxin-exposed glands, we counted “bursts” as five or more BrdU positive cells in a 20-cell radius.ResultsGrowth and development for the mammary gland is stimulated in two waves, the first occurs during pre-puberty (1? weeks of age, depending on the strain), when the ductal tree branches out from the placode to colonize the mammary fat pad. The second describes the full development of the lobulo-alveolar lineage during pregnancy. The vast 15857111 majority of cells that develop during pregnancy involute at the end of lactation, whereas the majority of ductal epithelial cells are likely to be long-lived in mice andPreparation of Mammary Epithelial Cells (MECs), Fat Pad Stem Cell Assay, Primary Culture Methods and Culture of HC11 CellsPrimary MECs were isolated as described and transferred to fat pads in 3 week-old recipient mice [17]. Data from limiting dilution assays were tested for statistical fit of clonogenic activity (usingGenotoxins Inhibit Wnt-Dependent Mammary Stem Cellwomen. To examine the interaction of environmental genotoxins with mammary gland.Nces) equipped with FlowJo software (Tree Star Inc. Ashland, OR). The gating profiles and trees are shown in Fig. S1A and B, and were generated according to [19].`Cell and Tissue Preparation for Western Blot AnalysisCells were rinsed with PBS and scraped into a high salt lysate buffer (25 mM HEPES pH 7.4, 300 mM NaCl, 1.5 mM MgCl2, 1 mM EGTA, and 0.5 Triton X100, with Halt protease and phosphatase inhibitor cocktails, Pierce, Rockford, IL). For tissues, mammary glands were snap frozen in liquid nitrogen and ground with a mortar and pestle. The resulting powder was mixed with high salt buffer containing protease and phosphatase inhibitors and homogenized for ten seconds, twice, at 4uC with a Polytron (Kinematica, AG, Switzerland). The resulting tissue and cell lysates were cleared for 20 min at 10 000 g at 4uC and the supernatant was analyzed by Western blotting. Antibodies used as probes were: anti-phospho-Lrp6 (detecting both phospho-Lrp6 and phospho-Lrp5; Cell Signaling Technology), anti-vinculin (Millipore), and anti-b-actin (clone AC-15, Sigma-Aldrich). Secondary antibodies were peroxidase-conjugated anti-mouse IgG (Jackson ImmunoResearch Laboratories, West Grove, PA) and horseradish peroxidase conjugated anti-rabbit IgG (InVitrogen).Whole Mount Staining and ImmunohistochemistryMammary glands were fixed and processed to visualize ductal trees as described [17]. General methods for immunohistochemical analysis of paraffin-embedded mammary samples include antigen retrieval as described [17]. Primary antibodies are: antiKi67 (BD Biosciences, Franklin Lakes, NJ), Keratin 5 Clone AF 138 (Covance, Emeryville, CA), Keratin 8 (The University of Iowa ?Developmental Studies Hybridoma Bank, Iowa City, Iowa), cH2AX (Millipore, Billerica, MN), BrdU (Roche, Indianapolis, IN), phospho-Ser15 p53 (Cell Signaling Technology, Beverly, MA). Secondary antibodies and reagents were: AlexaFluor 488 goat anti-mouse, AlexaFluor 546 goat anti-rat, AlexaFluor 488 goat anti-rabbit, AlexaFluor 647 goat anti-rabbit, Pacific Blue conjugated goat anti-rabbit (all from Invitrogen, Carlsbad, CA). To calculate the mitotic index of basal and luminal cells, paraffin sections of mammary glands from BrdU-injected mice were counterstained with lineage-specific markers (K5 and K8), together with a nuclear stain (to score the total cell number of each cell type). To describe the focalized nature of the excess mitotic index in genotoxin-exposed glands, we counted “bursts” as five or more BrdU positive cells in a 20-cell radius.ResultsGrowth and development for the mammary gland is stimulated in two waves, the first occurs during pre-puberty (1? weeks of age, depending on the strain), when the ductal tree branches out from the placode to colonize the mammary fat pad. The second describes the full development of the lobulo-alveolar lineage during pregnancy. The vast 15857111 majority of cells that develop during pregnancy involute at the end of lactation, whereas the majority of ductal epithelial cells are likely to be long-lived in mice andPreparation of Mammary Epithelial Cells (MECs), Fat Pad Stem Cell Assay, Primary Culture Methods and Culture of HC11 CellsPrimary MECs were isolated as described and transferred to fat pads in 3 week-old recipient mice [17]. Data from limiting dilution assays were tested for statistical fit of clonogenic activity (usingGenotoxins Inhibit Wnt-Dependent Mammary Stem Cellwomen. To examine the interaction of environmental genotoxins with mammary gland.