Which of the following statements related to intercellular junctions is false? O Cadherins are important cell-cell adhesion proteins. A cadherin-mediated junction involves many cadherin molecules to achieve strong adhesion. O The cytoplasmic domain of cadherins interacts with actin or intermediate filament cytoskeleton through adaptor proteins. Because tight junctions seal the membrane of adjacent epithelial cells, transmembrane proteins in the apical portion of the plasma membrane cannot move to the basal lateral domain or vice versa. O Proteins can diffuse through an open gap junction.

Which of the following statements related to intercellular junctions is false? O Cadherins are important cell-cell adhesion proteins. A cadherin-mediated junction involves many cadherin molecules to achieve strong adhesion. O The cytoplasmic domain of cadherins interacts with actin or intermediate filament cytoskeleton through adaptor proteins. Because tight junctions seal the membrane of adjacent epithelial cells, transmembrane proteins in the apical portion of the plasma membrane cannot move to the basal lateral domain or vice versa. O Proteins can diffuse through an open gap junction.

Human Physiology: From Cells to Systems (MindTap Course List)

9th Edition

ISBN:9781285866932

Author:Lauralee Sherwood

Publisher:Lauralee Sherwood

Chapter3: The Plasma Membrane And Membrane Potential

Section: Chapter Questions

Problem 7RE

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The tails of the phospholipids of the plasma membrane are composed of _____ and are _____? a. phosphate groups; hydrophobic b. fatty acid groups; hydrophilic c. phosphate groups; hydrophilic d. fatty acid groups; hydrophobic
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Organelles and Cystic Fibrosis A plasma membrane transport protein called CFTR moves chloride ions out of cells lining cavities and ducts of the lungs, liver, pancreas, intestines, and reproductive system. Water that follows the ions creates a thin film that allows mucus to slide easily through these structures. People with cystic fibrosis (CF) have too few copies of the CFTR protein in the plasma membranes of their cells. Not enough chloride ions leave the cells, and so not enough water leaves them either. The result is thick, dry mucus that clogs the airways to the lungs and other passages. Symptoms include difficulty breathing and chronic lung infections. In 2000, researchers tracked the cellular location of the CFTR protein as it was being produced in cells from people with CF (Figure 3.13). Figure 3.13 Cellular location of the CFTR protein. Graph compares the amounts of CFTR protein found in endoplasmic reticulum, vesicles travel in g from ER to Golgi, and Golgi bodies in CF cells and normal cells. Which organelle contains the least amount of CFTR protein in normal cells? In CF cells?
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