Chapter 2 - Cell Structure and Function PDF

Summary

This document presents information on the organization of a cell, its membrane components (lipids, proteins, carbohydrates, and cholesterol), organelles (including ribosomes, mitochondria, Golgi apparatus), and the functions of these structures. The document also discusses cell processes such as endocytosis and exocytosis.

Full Transcript

# Organization of the Cell - Cell Membrane - thin, pliable, elastic structure - 7.5 to 10 nanometers thick - composed almost entirely of proteins and lipids - The approximate composition is: - 55% proteins, 25% phospholipids, 13% cholesterol, 4% other lipids, and carbohy...

# Organization of the Cell - Cell Membrane - thin, pliable, elastic structure - 7.5 to 10 nanometers thick - composed almost entirely of proteins and lipids - The approximate composition is: - 55% proteins, 25% phospholipids, 13% cholesterol, 4% other lipids, and carbohydrates - Cytoplasm: the jelly-like fluid portion of the cytoplasm in which the particles are dispersed is called. - contains mainly dissolved proteins, electrolytes, and glucose - **Organelles:** - neutral fat globules, glycogen granules, ribosomes, secretory vesicles, and 5 especially important organelles - endoplasmic reticulum, Golgi apparatus, mitochondria, lysosomes, and peroxisomes ## Membranous Structures of the Cell - cell membrane - nuclear membrane - membrane of the endoplasmic reticulum, - Membranes of the mitochondria, - lysosomes, - Golgi apparatus ## Cell Membrane - Bilayer of Phospholipids with Proteins ### Membrane Components: - **LIPIDS:** barrier to water and water-soluble substances - **PROTEINS:** - provide "specificity" to a membrane - defined by mode of association with the lipid bilayer - **integral:** channels, pores, carriers, enzymes, etc. - **peripheral:** enzymes, intracellular signal mediators - **CARBOHYDRATES:** - glycolipids (approx. 10%) - glycoproteins (majority of integral roteins) - proteoglycans - **Cholesterol:** - present in membranes in varying amounts - generally decreases membrane FLUIDITY and PERMEABILITY (except in plasma membrane) - increases membrane FLEXIBILITY and STABILITY ## Cell Organelles **Centrioles** - a pair of small cylindrical structures located near the nucleus of a cell. They are involved in the formation of microtubules, which are part of the cytoskeleton and involved in cell division. **Secretory Granules** - small, membrane-bound sacs that contain substances to be secreted from the cell. **Microtubules** - hollow, cylindrical structures that provide support for the cell and help in the movement of organelles. **Nuclear Membrane** - a membrane that encloses the nucleus of eukaryotic cells. It regulates the movement of substances between the nucleus and the cytoplasm. **Chromosomes and DNA** - Genetic material of the cell. **Golgi Apparatus** - a stack of flattened, membrane-bound sacs that modify, package, and transport proteins and lipids. **Cell Membrane** - thin, pliable, elastic structure that surrounds the cell. **Nucleolus** - a small, dense body within the nucleus of a cell. It is involved in the production of ribosomes **Glycogen** - a complex carbohydrate that is stored as an energy reserve in the liver and muscles. **Ribosomes** - small, granular organelles that are involved in the synthesis of proteins. **Lysosome** - membrane-bound organelles that contain enzymes that break down waste material and cellular debris. **Mitochondrion** - a complex organelle that is responsible for the production of energy in the form of ATP. **Granular Endoplasmic Reticulum** - a network of interconnected membrane-bound sacs and tubules that are studded with ribosomes. It is involved in the synthesis of proteins and lipids, as well as in the folding of proteins. **Smooth Endoplasmic Reticulum** - a network of interconnected membrane-bound sacs and tubules without ribosomes. It is involved in the synthesis of lipids and steroids, as well as in the detoxification of drugs and toxins. **Microfilaments** -thin, threadlike structures that contribute to cell shape, muscle contraction, and cell division. ## Structure - **Membranous Structures:** - cell membrane, - nuclear membrane, - membrane of the endoplasmic reticulum, - Membranes of the mitochondria, - lysosomes, - Golgi apparatus ## Cell Membrane - is a thin, pliable, elastic structure - only 7.5 to 10 nanometers thick - It is composed almost entirely of proteins and lipids. ## Cytoplasm - The jelly-like fluid portion of the cytoplasm in which the particles are dispersed is called. - contains mainly dissolved proteins, electrolytes, and glucose ### Endoplasmic Reticulum - Network of tubular and flat vesicular structures - Membrane is similar to (and contiguous with) the plasma membrane - Space inside the tubules is called the endoplasmic matrix #### Rough or Granular ER - outer membrane surface covered with ribosomes - newly synthesized proteins are extruded into the ER matrix - proteins are "processed" inside the matrix - crosslinked - folded - glycosylated (N-linked) - cleaved #### Smooth ER - site of lipid synthesis - phospholipids - cholesterol - growing ER membrane, buds continuously forming transport vesicles, most of which migrate to the Golgi apparatus ### Golgi Apparatus - Membrane composition similar to that of the smooth ER and plasma membrane - Composed of 4 or more stacked layers of flat vesicular structures - Receives transport vesicles from smooth ER - Substances formed in the ER are "processed" - phosphorylated, glycosylated - Substances are concentrated, sorted and packaged for secretion. ### Exocytosis: - Secretory vesicles diffuse through the cytosol and fuse to the plasma membrane - Lysosomes fuse with internal endocytotic vesicles ### Secretion: - secretory vesicles containing proteins synthesized in the RER bud from the Golgi apparatus - fuse with plasma membrane to release contents. - constitutive secretion happens randomly - stimulated secretion requires trigger ### Lysosomes - vesicular organelle formed from budding Golgi - contain hydrolytic enzymes (acid hydrolases) - phosphatases - nucleases - proteases - lipid-degrading enzymes - lysozymes - digest bacteria ### Lysosomal Storage Diseases - Absence of one or more hydrolases. - not synthesized, inactive, or not properly sorted and packaged - Result: Lysosomes become engorged with undigested substrate - Examples: - Acid lipase A deficiency - I-cell disease (non-specific) - Tay-Sachs disease (HEX- ### Peroxisomes: - similar physically to lysosomes - two major differences: - formed by self-replication - they contain oxidases - Function: oxidize substances (e.g. alcohol) that may be otherwise poisonous. ### Secretory Granules - small, membrane-bound sacs that contain substances to be secreted from the cell. ### Mitochondria - Primary function: extraction of energy from nutrients - Outer membrane - Inner membrane - Crests - Matrix - Outer chamber - Oxidative phosphorylation enzymes ## The Cytoskeleton - **Intermediate Filaments:** - Comprised of cell-specific fibrillar monomers - (e.g. vimentin, neurofilament proteins, keratins, nuclear lamins) - **Microtubules:** - Heterodimers of alpha and beta tubulin - Make up spindle fibers, core of axoneme structure - **Thin Filaments:** - F-Actin - Make up "stress fibers" in non-muscle cells - **Thick Filaments:** - Myosin (types I and II) ## The Nuclear Membrane - The nuclear membrane is permeated by thousands of nuclear pores - 100 nm in diameter - functional diameter is 9 nm - (selectively) permeable to molecules of up to 44,000 MW - Nucleoplasm - Endoplasmic reticulum - Nucleolus - Nuclear envelope: outer and inner membranes - Chromatin material (DNA) - Cytoplasm ## The Nucleolus - Chromatin (condensed DNA) is found in the nucleoplasm. - one or more per nucleus - contains RNA and proteins - not membrane delimited - functions to form the granular subunits of ribosomes. ## Comparison of the Animal Cell with Precellular Forms of Life - 15 nm: Small virus - 150 nm: Large virus - 1 µm Bacterium - 350 mm: Rickettsia ## Receptor-mediated Endocytosis: - molecules attach to cell surface - receptors concentrated in clathrin-coated pits - receptor binding induces invagination - also ATP-dependent and involves recruitment of actin and myosin. ## Digestion of Substances in Pinocytotic or Phagocytic Vesicles - Lysosomes - Pinocytotic or phagocytic vesicle - Digestive vesicle - Residual body - Excretion ## Pinocytosis - begins when droplets of extracellular fluid containing dissolved solutes collect in a pit at the surface of the cell. - forming a vesicle that is drawn into the cytoplasm of the cell. - A lysosome, containing digestive enzymes, fuses with the vesicle. - Finally, the digestive enzymes break down the extracellular fluid, and the digested solutes are released into the cytoplasm. ## Phagocytosis: - begins when receptors on a phagocyte surface bind to large solid particles such as microbes, dead cells, and debris - binding action triggers the plasma membrane to extend finger-like projections, called pseudopods, around the bound particle, forming a vesicle, known as a phagosome. - The phagosome then fuses with a lysosome, which contains digestive enzymes. - The digestive enzymes break down the engulfed particles into smaller molecules, and any remaining undigested material is contained in a vesicle known as a residual body. ## Receptor-mediated Endocytosis: - binds to a specific receptor on the cell's plasma membrane, forming a ligand-receptor complex. - Each receptor is associated with a protein, known as a clathrin, on the membrane's cytoplasmic side. - The regions of the plasma membrane in which these receptors and their associated clathrin molecules collect are called clathrin-coated pits. - The clathrin-coated pit sinks into the cell, forming a vesicle that contains the ligand-receptor complexes. - The uncoated vesicle fuses with an endosome, and the ligands and receptors separate, collecting at opposite ends of the endosome. - Next, the endosome fuses with a lysosome containing digestive enzymes. ## Receptor-mediated endocytosis ### Lysosomes: - DIGEST PINOCYTOTIC AND PHAGOCYTIC FOREIGN SUBSTANCES INSIDE THE CELL - **Lysosomes:** Regression of Tissues and Autolysis of Damaged Cells. - If the damage is severe, the entire cell is digested, a process called autolysis. - The lysosomes also contain bactericidal agents that can kill phagocytized bacteria before they cause further damage. - These agents include the following: - **lysozyme,** which dissolves the bacterial cell wall; - **lysoferrin,** which binds iron and other substances before they can promote bacterial growth; and - **acid at pH 5.0,** which activates the hydrolases and inactivates bacterial metabolic systems. ## ATP Production - **Step 1.** - Carbohydrates are converted into glucose - Proteins are converted into amino acids - Fats are converted into fatty acids - **Step 2.** - Glucose, AA, and FA are processed into Acetyl CoA - **Step 3.** - Acetyl CoA reacts with O2 to produce ATP. - A maximum of 38 molecules of ATP are formed per molecule of glucose degraded. ## The Use of ATP for Cellular Function - under "standard" conditions ΔGo is only -7.3 kcal/mole - ATP concentration is ~10x that of ADP, the ΔG is -12 kcal/mole - Membrane transport - Synthesis of chemical compounds - Mechanical work ## Amoeboid Locomotion - continual endocytosis at the "tail" and exocytosis at the leading edge of the pseudopodium. - attachment of the pseudopodium is facilitated by receptor proteins carried by vesicles. - forward movement results through interaction of actin and myosin (ATP-dependent). ### Cell movement is influenced by - chemical substances... - Low concentration (negative) - Chemotaxis - High concentration (positive) ## Cilia and Ciliary Movements - Occurs only on the inside surfaces of the human airway and fallopian tubes - Each cilium is comprised of: - 11 microtubules - 9 double tubules - 2 single tubules - axoneme - Each cilium is an outgrowth of the basal body and is covered by an outcropping of the plasma membrane. - Ciliary movement is ATP-dependent. ## Amoeboid Locomotion: ## Mechanism of Ciliary Movement - Fourth, during forward movement on a cilia, the edge of the cilium slides those on the back edge - Fifth, multiple protein arms attach to the double tubule (adenosine triphosphate) - These structures are encircled by nine double fibers and a cellular membrane, a unique combination that enables motility. - Cilia and Flagella assist in fluid movement and in the locomotion of single cells. - In particular, single-celled organisms, such as paramecium and bacteria, move with the help of Cilia and Flagella, respectively. ## Non-motile Primary Cilia - Found on nearly every type of cell... (except RBC) - Primary cilia are non-motile and generally occur only as a single cilium on each cell. - Physiological functions of primary cilia are not fully understood. - current evidence indicates they function as cellular "sensory antennae," which coordinate: - cellular signaling pathways involved in chemical and mechanical sensation; - signal transduction, and - cell growth. - Prominent in retinal photoreceptors & renal epithelial cells (as mechanoreceptors) - **Motile Cili** - Solitary motile cilia (SMC) - Multiple motile cilia (MMC) - **Non-motile Cili** - Primary cilia - Pair of microtubules - Microtubule singlets - Radial spoke - Dynein arm - **Transversal View** ### "GOOD EVENING"

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