Cells are needed to see this picture. TIFF (LZW) decompressor QuickTime™ and a Advanced Biology Organization of the Cell • Cells are dramatic examples of the underlying unity of all living things. • Idea first expressed by Matthias Schleiden and Theodor Schwann in 1839. They concluded that plants & animals are made of cells. • Rudolf Virchow saw cells dividing and making daughter cells in 1855. Proposed cells only come from other cells. • August Weismann added to Virchows theory that the cell can be traced from ancient cells. • CELL THEORY: • 1. Cells are the basic living units of organization & function in all organisms. • 2. Cells come from other cells. Cell Organization • A cell is the smallest unit that can carry out all activities associated with life. • But no part of an isolated cell can survive. • A cell hardly gets NRG in the form it needs it to be in. It must be converted. Advances in technology helps us to better understand cells, their function & structure. Cell Organization and Size • Cell organization & size helps them maintain HOMEOSTASIS, stable internal environment. • A.) The organization of all cells is basically similar. • The plasma membrane, which is a membrane that surrounds all cells, helps keep cells separate from their external environment. • Plasma menbrane also serves as a SELECTIVE barrier of what enters & exist the cell. • Cells have ORGANELLS which carry out specialized functions. Cell Size • B.) Cell size is limited. • Most cells are too microscopic to see with the naked eye. • The small micrometer is too small to see & count the organelles of the cell, a nanometer is used instead. • A human egg can be seen with the naked eye, as big as a period in a sentence. • A cell is small because it is much easier to maintain homeostasis and do daily functions. • When a cell gets bigger, the volume increases faster than the surface area also putting a restriction on size. Cell Size QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Cell Shape & Function • Not all cells are spherical or cuboid. • Fingerlike projections from the plasma membrane are called Microvilli, increase the surface area for absorption. • Some cells can change shape to accommodate a function. • Also small because molecules inside must travel distances. • This distance is smaller when the cell is small. • C.) Cell size & shape are related to function • Size & shape are related to the function of a cell. • Examples: sperm, epithelial cells, nerve cells. Methods for Studying Cells • One of the most important tools is the microscope. • In 1665, Robert Hook discovered cells when he observed dead cork and said they reminded him of the rooms monks lived in. • Anton von Leeuwenhoek designed a good lens for microscopes a few years later and improved microscopy. Cork cells QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. A.) Light microscopes are used to study stained cells • Light microscope has a tube with glass lenses at each end, also called a compound microscope. • Magnification is the ratio of size of image to actual size, usually no more than 1000X. • Resolution is the capacity to distinguish detail. • Minimum space where two individual points can be seen, not blurry. • Bright-field uses light. • Dark-field has scattered light. • Phase contrast & differential interference contrast uses density. • Fluorescence looks at molecular structure of cells. B.) Electron Microscope • Ultra-structure is fine detail. • Electron microscopes magnify up to 1/4 million times. • Transmission Electron Microscope (TEM) requires that the specimen is enbeded in plastic & cut into very thin strips to produce layered images. • Scanning Electron Microscope (SEM) requires that the specimen is coated in metal and an indirect beam of electrons creates a 3-D image of the surface. Microscopes QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. C.) Cell Fractionation enables study of cell organelles • Cell fractionation is purifying organelles. • Centrifuge spins broken cells to form a pellet. • Pellet forms at bottom and supernatant is at the top of solution. • The supernatant is spun again in differential centrifugation, at higher speeds. • Pellets are further purified in density gradient centrifugation. Cell Fractionation QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Prokaryotic & Eukaryotic cells • Prokaryotes do not have DNA in a nucleus but in a nuclear area or Nucleoid, no membrane. • Prokaryote means before the nucleus. • Many prokaryotes have cell walls and flagella & have ribosomes. • Eukaryotes are highly organized, advanced cells. • Eukaryote means true nucleus. • Cells are filled with a jelly-like substance called protoplasm. • Outside nucleus is called cytosol. • Inside nucleus is called nucleoplasm. • Organelles in cytosol = cytoplasm. Cell Membrane • Lets things in & out of cell, keeps certain things away from other parts of the cell. • Membranes are work surfaces that store energy. • Endomembrane systems are all internal membranes. • Some materials travel in vesicles. Anatomy of a Cell Membrane • A bi-phospholipid layer with integral proteins throughout. • Is Amphipathic due to hydrophobic & hydrophilic regions. • 2-D fluid, cannot move without channel. • Lots of saturated fatty tails, become more solid. • Unsaturated, bends where double bonds exist. • Cholesterol acts as a buffer, either keeps tails apart or brings them closer together. • Cholesterol makes the membrane more fluid at lower temperature. Types of membrane Proteins • • • • • • • Receptor- recieves materials Channel-lets things travel from one protein to another. Enzymes- breaks down unwanted materials Carrier- allows specific materials& ions to pass in & out Recognition- identifies Signal- gives signal for what is needed. Aquaporins- gated water channels Anatomy of a Cell Membrane QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Methods of Movement across Membranes with no NRG • Passive Transport- no NRG needed • Diffusion- particles randomly move from high concentrations to low concentrations • Osmosis- diffusion of water through a membrane • Facilitated Diffusion- carrier protein facilitates the movement of certain ions or other polar molecules from high concentration to low. • A Concentration Gradient is created when there is different concentration of a substance on each side of a membrane. Diffusion & Osmosis QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Isotonic, Hypertonic, & Hypotonic Solutions QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. • Isotonic- same concentration of solutes on both sides of membrane, Equal movement of water. • Hypertonic- more solute on outside of cell membrane. Movement of water is out of cell. • Hypotonic- less solute on outside of cell. Movement of water is into cell Plasmolysis QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. • Loss of turgor pressure • Water potential is from inside cell to outside • Caused by putting cells in a hypertonic solution. • Causes plant to wilt Facilitated Diffusion QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Methods of Movement across Membranes with NRG required • Active Transport- ATP energy required • Sodium-Potassium Pump- a carrier mediated active transport system that imports 2 potassium cations into the cell and exports 3 sodium cations. • This creates an unequal charge (Electrical gradient) due to more positive charge on outside cell membrane. • This also creates a Membrane Potential because of the concentration difference and charge difference. • Important in nerve impulses. • Endocytosis- taking in large particles by fusion to the cell memnbrane to create a vacuole. (phago & pinocytosis) • Exocytosis- ridding large particles by fusion of a vesicle to the cell membrane. Sodium-Potassium Pump QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Types of Endocytosis • Phagocytosis- cell eating (WBC & bacteria) • Once inside, the large substance is digested by lysosome enzymes. • Pinocytosis- cell drinking • Tiny droplets are taken in by folds in the membrane that trap & pinch off inside. • Receptor- mediated endocytosis- special receptor molecule called ligands combind with specific molecules on a coated pit & forms a coating around it before it pinches off inside the cell. Exocytosis, Phagocytosis, & Pinocytosis QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Receptor-Mediated Endocytosis QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Cell Signaling • Mechanisms by which cells communicate with one another. • Most often use chemicals. • Signaling molecule from one cell will combine with a receptor on another cell. • Example: cAMP,&neurotransmitters are signaling molecules, GTP is a receptor molecule. • Enzymes are also used to catalyze the production on secondary messenger molecules. See fig. 5-21 • Signal Transduction is a process where cells convert and amplify an extracellular signal into an intracellular signal Cell Junctions • Special intercellular connections • Allow neighboring cells to do one or more of the following: • form strong connections • prevent passage of materials • communicate with each other. Types of Cell Junctions • • • • • • • • 1.) Anchoring Junctions Tightly bound to each other. Example: epithelial cells in the outer skin. Cadherins are transmembrane proteins that play an important role in these junctions. Two types of anchoring junctions: Desmosomes & Adhering junctions. Adhering junctions cement cells together. Cadherins form a continuous adhesion belt around each cell connecting the microfilaments of the cytoplasm Create a path for signaling from outside to inside cell. Desmosomes QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. • Form points of attachment between cells like rivets. • Substances still pass freely through the space between the membranes. • Anchor to intermediate filaments inside the cell. Cell Junctions cont. • 2.) Tight Junctions • Seal off intercellular spaces between some animal cells. • No space remains between cells. • Substances cannot leak between them. • Seal off body cavities. • Example: lining of intestine, blood-brain barriers Cell Junctions cont. • 3.) Gap Junctions • Bridges the space between cell but leaves very narrow spaces. • Are communicating junctions. • Contain channels that connect the cytoplasms of adjacent cells. • Composed of connexin, an integral membrane protein. • Groups of 6 connexin molecules cluster to form a cylinder that spans the plasma membrane. • Small organic molecules, ions, and cAMP pass through the channels. • Allow for rapid chemical & electrical communication. Tight junctions & Gap Junctions Gap Junction QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Tight Junction QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. Cell Junctions cont. QuickTime™ and a TIFF (LZW) decompressor are needed to see this picture. • • • • • 4.) Plasmodesmata Formed between plant cells. Form between cell walls. Connect the cytoplams. Form cylindrical membranous structures called desmotubule that connect the ER of ajacent cells. • Allow molecule & ions to pass, not organelles. • Can dilate their diameters.