B- How can the following material pass through plasma Membrane? 1- Co2 2- amino acids 3- enzymes 4-ions 5- hormones

Cytoplasmic extensions of _______ send and receive chemical messages. a. neuroglial cells b. neurons c. fibroblasts d. melanocytes

Which of the following statements is false? Proteins in the plasma membrane can: a. transport ions. b. transport chloride ions when there are two mutant copies of the cystic fibrosis transmembrane conductance regulator gene. c. recognize self versus foreign molecules. d. allow adhesion between the same tissue cells or cells of different tissues. e. combine with lipids or sugars to form complex macromolecules.

Which plasma membrane component can be either found on its surface or embedded in the membrane structure? a. protein b. cholesterol c. carbohydrate d. phospholipid

In the fluid mosaic model: plasma membrane proteins orient their hydrophilic sides toward the internal bilayer. phospholipids often flip-flop between the inner and outer layers. the mosaic refers to proteins attached to the underlying cytoskeleton. the fluid refers to the phospholipid bilayer. the mosaic refers to the symmetry of the internal membrane proteins and sterols.

Figure 4.8 If the nucleolus were not able to carry out its function, what other cellular organelles would be affected?

Active transport must function continuously because_______. a. plasma membranes wear out b. cells must be in constant motion c. facilitated transport opposes active transport d. diffusion is constantly moving the solutes in the other direction

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?

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 traveling from ER to Golgi, and Golgi bodies in CF cells and normal cells. In which organelle is the amount of CFTR protein most similar in both types of cells?

Which type of epithelial cell is best adapted to aid diffusion? squamous cuboidal columnar transitional