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 11 - Section 11.7 - Study Guide - Assess Your Learning Outcomes - Page 433: 10

Answer

Smooth muscle myocytes have a distinct structural organization compared to striated muscle (skeletal and cardiac) myocytes. While smooth muscle lacks the well-defined Z discs and T tubules found in striated muscle, it possesses unique structures that serve similar functions in the absence of these features: **Structure of Smooth Muscle Myocytes**: 1. **Myofilaments**: Like striated muscle, smooth muscle contains myofilaments, which are contractile proteins responsible for muscle contraction. These myofilaments consist of actin and myosin filaments arranged in a crisscross pattern. 2. **Intermediate Filaments**: Smooth muscle myocytes contain intermediate filaments composed of the protein desmin. These intermediate filaments serve to anchor the contractile proteins and maintain the structural integrity of the cell. 3. **Dense Bodies**: - Dense bodies are structures analogous to Z discs in striated muscle. They anchor the thin filaments (actin) in place within the cell. - Dense bodies are dispersed throughout the cytoplasm of the smooth muscle cell and serve as attachment points for actin filaments. 4. **Caveolae**: - Smooth muscle cells have invaginations in their cell membrane called caveolae. These serve a similar function to T tubules in striated muscle by allowing for the rapid exchange of calcium ions (Ca2+), which is crucial for muscle contraction. - Caveolae play a role in the regulation of calcium concentration within the cell. 5. **Sarcoplasmic Reticulum (SR)**: - Smooth muscle cells have a less developed sarcoplasmic reticulum compared to striated muscle. However, they do contain some SR, which is responsible for storing and releasing calcium ions. - The release of calcium from the SR is a critical step in initiating smooth muscle contraction. 6. **Calmodulin and Myosin Light Chain Kinase (MLCK)**: - Smooth muscle contraction is regulated by the binding of calcium ions to the protein calmodulin, which then activates the enzyme myosin light chain kinase (MLCK). - MLCK phosphorylates the myosin light chains, allowing for myosin-actin interactions and muscle contraction. 7. **Non-Striated Appearance**: - Unlike striated muscle, smooth muscle myocytes lack the clear striations seen in skeletal and cardiac muscle due to the absence of highly organized sarcomeres. In summary, smooth muscle myocytes have a unique structural organization that allows them to function effectively despite the absence of Z discs and T tubules. Dense bodies serve as anchoring points for actin filaments, while caveolae facilitate calcium ion exchange, and the sarcoplasmic reticulum stores and releases calcium. The regulation of smooth muscle contraction relies on the interaction between calmodulin, MLCK, and myosin light chains. This structural adaptation allows smooth muscle cells to contract in a coordinated manner for various physiological functions, such as regulating the diameter of blood vessels, the movement of substances through the digestive tract, and other essential processes in the body.

Work Step by Step

Smooth muscle myocytes have a distinct structural organization compared to striated muscle (skeletal and cardiac) myocytes. While smooth muscle lacks the well-defined Z discs and T tubules found in striated muscle, it possesses unique structures that serve similar functions in the absence of these features: **Structure of Smooth Muscle Myocytes**: 1. **Myofilaments**: Like striated muscle, smooth muscle contains myofilaments, which are contractile proteins responsible for muscle contraction. These myofilaments consist of actin and myosin filaments arranged in a crisscross pattern. 2. **Intermediate Filaments**: Smooth muscle myocytes contain intermediate filaments composed of the protein desmin. These intermediate filaments serve to anchor the contractile proteins and maintain the structural integrity of the cell. 3. **Dense Bodies**: - Dense bodies are structures analogous to Z discs in striated muscle. They anchor the thin filaments (actin) in place within the cell. - Dense bodies are dispersed throughout the cytoplasm of the smooth muscle cell and serve as attachment points for actin filaments. 4. **Caveolae**: - Smooth muscle cells have invaginations in their cell membrane called caveolae. These serve a similar function to T tubules in striated muscle by allowing for the rapid exchange of calcium ions (Ca2+), which is crucial for muscle contraction. - Caveolae play a role in the regulation of calcium concentration within the cell. 5. **Sarcoplasmic Reticulum (SR)**: - Smooth muscle cells have a less developed sarcoplasmic reticulum compared to striated muscle. However, they do contain some SR, which is responsible for storing and releasing calcium ions. - The release of calcium from the SR is a critical step in initiating smooth muscle contraction. 6. **Calmodulin and Myosin Light Chain Kinase (MLCK)**: - Smooth muscle contraction is regulated by the binding of calcium ions to the protein calmodulin, which then activates the enzyme myosin light chain kinase (MLCK). - MLCK phosphorylates the myosin light chains, allowing for myosin-actin interactions and muscle contraction. 7. **Non-Striated Appearance**: - Unlike striated muscle, smooth muscle myocytes lack the clear striations seen in skeletal and cardiac muscle due to the absence of highly organized sarcomeres. In summary, smooth muscle myocytes have a unique structural organization that allows them to function effectively despite the absence of Z discs and T tubules. Dense bodies serve as anchoring points for actin filaments, while caveolae facilitate calcium ion exchange, and the sarcoplasmic reticulum stores and releases calcium. The regulation of smooth muscle contraction relies on the interaction between calmodulin, MLCK, and myosin light chains. This structural adaptation allows smooth muscle cells to contract in a coordinated manner for various physiological functions, such as regulating the diameter of blood vessels, the movement of substances through the digestive tract, and other essential processes in the body.
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