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DR. NUR FARIESHA MD HASHIM MSc Radiation Biology (UCL), PhD Cancer Cell Biology (KCL)
PHYSIOLOGY UNIT, DEPT. OF BIOMEDICAL SCIENCE, FACULTY OF MEDICINE & HEALTH SCIENCES UPM
All new cells and new life arise only from preexisting cells
The functional activities of each cell depend on the specific structural properties of the cell
Because of this continuity of life, the cells of all organisms are fundamentally similar in structure and function
An organisms structure and function ultimately depend on the collective structural characteristics and functional capabilities of its cells
PART 1
Cell Structure
Different cells share many common features. Most cells have 3 major subdivisions:
Plasma membrane
Encloses the cells Contains the cells genetic material The portion of the cells interior not occupied by the nucleus
Nucleus
Cytoplasm
Plasma membrane
It keeps the intracellular fluid (ICF) within cells from mingling with the extracellular fluid (ECF) outside the cells
Like gated walls that enclosed ancient cities, the cell controls the entry of nutrients and other needed supplies and the export of products manufactured within
1-Typically the largest single organized cell component located near the center of the cell
2-Surrounded by nuclear envelope- separates the nucleus from the rest of the cell
Nucleus
4-DNA has 2 major functions: directing protein synthesis and serves as genetic blueprint during cell replication
Cytoplasm
Organelles
Cytoskeleton
Cytosol
PART 2
Rough ER
Consists of stacks of relatively flattened interconnected sacs Synthesizes glycoproteins and phospholipids that are transferred into cellular organelles, inserted into the plasma membrane, or secreted during exocytosis
Smooth ER
Is a meshwork of tiny interconnected tubules Synthesizes fatty acids and steroids, such as estrogens and testosterone; inactivates or detoxifies drugs and other potentially harmful substances; removes the phosphate group from glucose-6-phosphate; and stores and releases calcium ions that trigger contraction in muscle cells
The outer surface of RER membrane is studded with small particles called ribosomes- the workbenches where protein synthesis takes place
The rough endoplasmic reticulum synthesizes proteins for secretion and membrane construction
The RER synthesizes and releases a variety of new proteins which serve one of 2 purposes : 1-some proteins are destined for export to the cells exterior as secretory products, like protein hormones or enzymes 2- other proteins are transported to sites within the cell for constructing new cellular membrane
The RER is most abundant in cells specialized for protein secretion (i.e. cells that secrete digestive enzymes) or in cells that require extensive membrane synthesis (i.e. rapidly growing cells like immature egg cells)
No ribosomes. SER is rather sparse and primarily serves as a central packaging and discharge site for molecules to be transported from the ER
The smooth endoplasmic reticulum packages new proteins in transport vesicles
Portions of the SER then bud off (balloon outward on the surface, then are pinched off), forming transport vesicles that enclose the new molecules in a spherical capsule derived from SER membrane Vesicle= fluid-filled, membrane enclosed intracellular cargo container
1-The RER synthesizes proteins to be secreted to the exterior or to be incorporated into cellular membrane
6-On appropriate stimulation, the secretory vesicles fuse with the plasma membrane, open, and empty their contents to the cells exterior. Secretion has occurred by exocytosis, with the secretory products never having come in contact with the cytosol
2-The SER packages the secretory product into transport vesicles, which bud off and move to the Golgi complex
5-Secretory vesicles containing the finished protein products bud off the Golgi complex and remain in the cytosol, storing the products until signaled to empty
3-The transport vesicles fuse with the Golgi complex , open up, and empty their contents into the closest Golgi sac
4-The newly synthesized proteins from the ER travel by vesicular transport through the layers of the Golgi complex, which modifies the raw proteins into final form and sorts and directs the finished products to their final destination by varying their wrappers
PART 3
Golgi Complex
Consists of a stack of slightly curved, membrane-enclosed sacs. The vesicles at the dilated edges of the sacs contain finished protein products packaged for distribution to their final destination
Processing and packaging of proteins by the Golgi complex. All proteins exported from the cell are processed in the Golgi complex
(b) Endocytosis: Materials from the cell exterior are enclosed in a segment of the plasma membrane that pockets inward and pinches off as an endocytic vesicle
PART 4
4- Lysosome fuses with vesicle, releasing enzymes that attack material inside vesicle
1- Solute molecules and water molecules are outside the plasma membrane
A highly selective process that enables cells to import specific large molecules that it needs from its environment
To be continued in CELL II
PART 5
The bilayer arrangement occurs because the lipids are amphipathic molecules = they have both polar and nonpolar parts
In phospholipids, the polar part is the phosphatecontaining head, which is hydrophilic water-loving
The non-polar parts are the 2 long fatty acid tails, which are hydrophobic water-fearing hydrocarbon chains
Because like seeks like, the phospholipid molecules orient themselves in the bilayer with their hydrophilic heads facing outward
In this way, the heads face a watery fluid on either side- cytosol on the inside and ECF on the outside
The hydrophobic fatty acid tails in each half of the bilayer point toward one another, forming a nonpolar, hydrophobic region in the membranes interior
Passive processes
Simple diffusion
Facilitated diffusion
Facilitated diffusion
Principle of osmosis
PART 6
In other words, they produce and decompose hydrogen peroxide (H2O2) in the process of degrading toxic molecules (peroxi = H2O2)
The major byproduct of oxidation is H2O2. Hydrogen peroxide is potentially destructive if allowed to accumulate or escape from peroxisomes
Peroxisomes are abundant in the liver, where detox of alcohol and other damaging substances occurs
This helps detoxify various wastes produced within the cell or foreign toxic compounds that entered the cell, like alcohol in beverages
So basically, peroxisomes protect other parts of the cell from the toxic effects of H2O2
The electron transport proteins embedded in the cristae are responsible for converting the energy of food into a usable form
Are referred to as the powerhouses of the cell, becoz they generate most of the ATP through aerobic respiration
Active cells, like those found in the muscles, liver and kidneys, use ATP at high rate have plenty mitochondria
Cells must extract energy from food nutrients and convert it into a usable formATP which consists of adenosine with 3 phosphate groups
Synthesis of some proteins needed for mitochondria functions occurs on the ribosomes present in the mitochondria matrix
In most cells, ATP is generated from the sequential dismantling of absorbed nutrient molecules in 3stages: glycolysis in the cytosol, citric acid cycle in the mitochondrial matrix and oxidative phosphorylation in the mitochondrial inner membrane
The elaborate folds of the cristae provide an enormous surface area for the chemical reactions that are part of the aerobic phase of cell respirationthe reactions that produce most of a cells ATP
Like peroxisomes, mitochondria selfreplicate that occurs during times of increased cellular energy demand
Centrioles
Are a pair of short cylindrical structures that lie at right angles to each other at the centrosome center. It is the cells main microtubule organizing center
Microtubules
Anchor many of the membranous organelles and serve as highways along which vesicles are transported within the cell by molecular motors
Centrosomes: Located near the nucleus, the centrosome consists of a pair of centrioles and pericentriolar material
A cilium contains a core of microtubules with one pair in the center surrounded by 9 clusters of doublet microtubules