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Lymph node: secondary nodule

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x

Secondary nodule <p>This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x</p>

Secondary nodule

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x

Germinal center <p>This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x</p>

Germinal center

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x

 - Dark zone <p>This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x</p>

- Dark zone

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x

 - Light zone <p>This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x</p>

- Light zone

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x

Mantle <p>This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x</p>

Mantle

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x

Capsule <p>This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x</p>

Capsule

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x

Subcapsular sinus <p>This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x</p>

Subcapsular sinus

This secondary nodule demonstrates the zonation visible within the germinal center. In the dark zone, B cells proliferate and undergo random mutations of their antibody-producing genes. These B cells are then selected in the light zone, based on their antibody’s ability to bind to an antigen. Those with high-affinity antibodies undergo further proliferation and form large, pale-staining immunoblasts. Prodigy of these cells become plasma cells and B memory cells. Cells with disadvantageous mutations are eliminated by apoptosis and phagocytosis by macrophages. Lymph node, 200x