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The cytosol is a clear, viscous, watery colloid that bathes the cytoskeleton and organelles. It contains enzymes, other proteins, amino acids, ATP, electrolytes, other diverse organic and inorganic ions, oxygen, carbon dioxide, and metabolic wastes. It is the site of glycolysis, anaerobic fermentation, and most protein synthesis.
The cytoskeleton is a network of protein filaments and cylinders that structurally support a cell, determine its shape, organize its contents, direct the movement of materials within the cell, and contribute to movements of the cell as a whole. It is connected to transmembrane proteins of the plasma membrane, and they in turn are connected to protein fibers external to the cell, creating a strong structural continuity from extracellular material to the cytoplasm.
Cytoskeletal elements even connect to chromosomes in the nucleus, enabling physical tension on a cell to move nuclear contents, mechanically stimulate genetic function, and influence the timing of cell division relative to cell size.
The cytoskeleton is composed of microfilaments, intermediate filaments, and microtubules. If you think of intermediate filaments as being like the stiff rods of uncooked spaghetti, you could, by comparison, think of microfilaments as being like fine angel-hair pasta and microtubules like tubular penne pasta.
Microfilaments (thin filaments) are about 6 nm thick and are made of the protein actin. They are widespread throughout the cell but especially concentrated in a fibrous mat called the terminal web (membrane skeleton) on the cytoplasmic side of the plasma membrane.
The phospholipids of the plasma membrane spread out over the terminal web like butter on a slice of bread. The web, like the bread, provides physical support, whereas the lipids, like butter, provide a permeability barrier.
It is thought that without the support of the terminal web, the phospholipids would break up into little droplets and the plasma membrane wouldn't hold together. As described earlier, actin microfilaments also form the supportive cores of the microvilli and play a role in cell movement.
Through its role in -----, actin plays a crucial role in embryonic development, muscle contraction, immune function, wound healing, cancer metastasis, and other processes that involve cell migration. cell motility
Intermediate filaments (8-10 nm thick) are thicker and stiffer than microfilaments. They give the cell its shape, resist stress, and form junctions that attach cells to their neighbors. In epidermal cells, they are made of the tough protein keratin and occupy most of the cytoplasm. They are responsible for the strength of hair and fingernails.
Microtubules (25 nm in diameter) are cylinders made of 13 parallel strands called protofilaments. Each protofilament is a long chain of globular proteins called tubulin
Microtubules radiate from an area of the cell called the centrosome. They hold organelles in place, form bundles that maintain cell shape and rigidity, and act like monorail tracks for motor proteins carrying organelles and macromolecules to specific destinations in the cell.
Microtubules form the axonemes of cilia and flagella and are responsible for their beating movements, and form the mitotic spindle that guides chromosome movement during cell division. Microtubules aren't permanent structures. They come and go moment by moment as tubulin molecules assemble into a tubule and then break apart again to be used somewhere else in the cell. The microtubules in cilia, flagella, basal bodies, and centrioles, however, are more stable.
Organelles (literally, "little organs") are to the cell what organs are to the body-structures that play individual physiological roles in the survival of the whole.
There is no universally agreed definition of the word organelle. Some authorities include cilia, microvilli, and even the plasma membrane in this concept, whereas others exclude intracellular structures such as ribosomes and centrioles because they're not enclosed in membranes.
This book, however, regards organelles as the intracellular structures, above the molecular level of complexity, that play indispensable roles in cellular metabolism. Some organelles are surrounded by membranes and are therefore referred to as membranous organelles.
membranous organelles. These are the nucleus, mitochondria, lysosomes, peroxisomes, endoplasmic reticulum, and Golgi complex.
Organelles without membranes include ribosomes, proteasomes, centrosomes, centrioles, and basal bodies.
The nucleus (fig. 3.26) is usually the largest organelle and the only one clearly visible with the light microscope. It contains the cell's chromosomes and is therefore the genetic control center of cellular activity.
It is typically spheroidal to elliptical in shape and about 5 µm in diameter. Most cells have a single nucleus, but there are exceptions
Mature red blood cells have none; they are anuclear. A few cell types are multinuclear.
Many cells of the liver, urinary bladder, and heart have two nuclei; bone-dissolving cells called osteoclasts have as many as 50; and a single skeletal muscle cell can have many thousands.
The Nucleus as Seen by Electron Microscopy. These photomicrographs were made by different TEM methods to show the internal structure of the nucleus and surface of the nuclear envelope. (a) Interior of the nucleus. (b) Surface of the nucleus, showing clusters of nuclear pores
The nucleus is enclosed in a double membrane, the nuclear envelope. The envelope is perforated with nuclear pores formed by a ring of proteins called the nuclear pore complex.
Nuclear Pore Complex These proteins regulate molecular traffic through the envelope and act like a rivet to hold the two membrane layers together. Hundreds of molecules pass through the nuclear pores every minute
Coming into the nucleus are raw materials for DNA and RNA synthesis, enzymes that are made in the cytoplasm but function in the nucleus, and hormones and other chemical messengers that activate certain genes. Going the other way, RNA is made in the nucleus but leaves to perform its job in the cytoplasm.
Why do these nuclear pores have to be larger in diameter than the channels in the cell's plasma membrane? Large molecules such as enzymes and RNA must pass through the nuclear pores, but pores in the plasma membrane must be small enough to prevent such large molecules from escaping the cell.
Immediately inside the ------ is a narrow but densely fibrous zone called the nuclear lamina, composed of a web of intermediate filaments. nuclear envelope
It supports the nuclear envelope and pores, provides points of attachment and organization for the chromosomes inside the nucleus, and plays a role in regulating DNA replication and the cell life cycle. nuclear lamina
Abnormalities of its structure or function are associated with certain nuclear lamina
The material in the nucleus is called nucleoplasm. This includes chromatin [3, 4] -fine threadlike matter composed of DNA and protein- and one or more dark-staining masses called nucleoli (singular, nucleolus, where ribosomes are produced.
Created by: Russells3709
 

 



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