Anatomy & Physiology: The Unity of Form and Function, 7th Edition

Published by McGraw-Hill Education
ISBN 10: 0073403717
ISBN 13: 978-0-07340-371-7

Chapter 21 - Section 21.3 - Study Guide - Assess Your Learning Outcomes - Page 844: 8

Answer

The life history of B lymphocytes, or B cells, involves a series of developmental stages that take place primarily in the bone marrow, where B cells are generated and mature. B cells play a crucial role in the humoral immune response by producing antibodies and providing long-term immunity through memory cells. Here's an overview of their life history: **1. Origin in the Bone Marrow:** B cells originate from hematopoietic stem cells in the bone marrow. These stem cells undergo a series of differentiation steps to become B cell precursors, known as pro-B cells. **2. Negative Selection:** During negative selection in the bone marrow, B cells that have receptors (B cell receptors or BCRs) that strongly bind to self-antigens are eliminated. This helps to prevent B cells from producing antibodies against the body's own tissues, reducing the risk of autoimmune responses. **3. Positive Selection and Maturation:** B cells that have BCRs with moderate affinity for self-antigens undergo positive selection. This process ensures that B cells are capable of recognizing a wide range of antigens. After positive selection, B cells mature and continue to express their unique BCRs. **4. Dispersal to Secondary Lymphoid Organs:** Mature B cells exit the bone marrow and migrate to secondary lymphoid organs, such as lymph nodes and the spleen. In these organs, B cells are ready to encounter antigens and initiate immune responses. **5. Activation and Differentiation:** When a mature B cell encounters its specific antigen, the antigen binds to its BCR, triggering activation. The activated B cell undergoes clonal expansion, proliferating to form a population of identical B cells, called plasma cells. Plasma cells are responsible for producing and secreting large amounts of antibodies specific to the encountered antigen. **6. Memory B Cell Formation:** In addition to differentiating into plasma cells, some activated B cells become memory B cells. Memory B cells have the ability to "remember" the specific antigen encountered, allowing for a rapid and robust response if the same antigen is encountered again in the future. **7. Humoral Immune Response:** Plasma cells play a central role in the humoral immune response by secreting antibodies into the bloodstream. Antibodies recognize and neutralize antigens, marking them for destruction by other immune cells. **8. Long-Term Immunity:** Memory B cells provide long-term immunity. If the same antigen is encountered later, memory B cells can quickly differentiate into plasma cells, leading to a faster and more effective immune response compared to the initial response. In summary, B cells undergo a series of developmental stages, including negative and positive selection in the bone marrow, maturation, activation, and differentiation upon encountering antigens. The formation of plasma cells and memory B cells ensures the production of antibodies and long-term immunity against specific antigens.

Work Step by Step

The life history of B lymphocytes, or B cells, involves a series of developmental stages that take place primarily in the bone marrow, where B cells are generated and mature. B cells play a crucial role in the humoral immune response by producing antibodies and providing long-term immunity through memory cells. Here's an overview of their life history: **1. Origin in the Bone Marrow:** B cells originate from hematopoietic stem cells in the bone marrow. These stem cells undergo a series of differentiation steps to become B cell precursors, known as pro-B cells. **2. Negative Selection:** During negative selection in the bone marrow, B cells that have receptors (B cell receptors or BCRs) that strongly bind to self-antigens are eliminated. This helps to prevent B cells from producing antibodies against the body's own tissues, reducing the risk of autoimmune responses. **3. Positive Selection and Maturation:** B cells that have BCRs with moderate affinity for self-antigens undergo positive selection. This process ensures that B cells are capable of recognizing a wide range of antigens. After positive selection, B cells mature and continue to express their unique BCRs. **4. Dispersal to Secondary Lymphoid Organs:** Mature B cells exit the bone marrow and migrate to secondary lymphoid organs, such as lymph nodes and the spleen. In these organs, B cells are ready to encounter antigens and initiate immune responses. **5. Activation and Differentiation:** When a mature B cell encounters its specific antigen, the antigen binds to its BCR, triggering activation. The activated B cell undergoes clonal expansion, proliferating to form a population of identical B cells, called plasma cells. Plasma cells are responsible for producing and secreting large amounts of antibodies specific to the encountered antigen. **6. Memory B Cell Formation:** In addition to differentiating into plasma cells, some activated B cells become memory B cells. Memory B cells have the ability to "remember" the specific antigen encountered, allowing for a rapid and robust response if the same antigen is encountered again in the future. **7. Humoral Immune Response:** Plasma cells play a central role in the humoral immune response by secreting antibodies into the bloodstream. Antibodies recognize and neutralize antigens, marking them for destruction by other immune cells. **8. Long-Term Immunity:** Memory B cells provide long-term immunity. If the same antigen is encountered later, memory B cells can quickly differentiate into plasma cells, leading to a faster and more effective immune response compared to the initial response. In summary, B cells undergo a series of developmental stages, including negative and positive selection in the bone marrow, maturation, activation, and differentiation upon encountering antigens. The formation of plasma cells and memory B cells ensures the production of antibodies and long-term immunity against specific antigens.
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