Cell Compartmentalization

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    CELL

    COMPARTMENTALIZATION

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    COMPARTMENTALISATION IN EUKARYOTIC

    CELLS

    Cellular compartments in cell biology comprise allof the closed parts within the cytosol of a

    eukaryotic cell, usually surrounded by a singleor double lipid layer membrane.

    Major compartments in eukaryotic cellsare cytosol (gray), endoplasmic reticulum, Golgiapparatus, nucleus, mitochondrion, endosome,lysosome, and peroxisome. These are isolated fromrest of the cell by atleast one layer of membrane.

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    MAJOR CELLULAR COMPARTMENTS

    The nuclear compartment comprisingthe nucleus

    The intercisternal space Organelles

    The cytosol

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    LOCATION OF COMPARTMENTS

    Characteristic distributions depend on interactions of theorganelles with the cytoskeleton and with one another.

    Golgi apparatus is located close to the nucleus, whereas thenetwork of ER tubules extends from the nucleus throughoutthe entire cytosol.

    For protein synthesis, all the organs used for it are relativelynear one another, the nucleolus makes the ribosomes whichsynthesize the proteins, the rough endoplasmic

    reticulum (rough ER) is near the nucleus as well. The Golgibody is also near the rough ER for packaging andredistributing.

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    FUNCTIONS

    Isolation of important cell functions.

    Intracellular pH, different enzyme

    systems, and other differences areisolated. This enables the cell to carry outdifferent metabolic activities at the same

    time. Provides cell with functionally

    specialized aqueous spaces.

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    Continued.

    Increases surface area.

    Compartmentalization allows

    eukaryotic cells to perform otherwiseincompatible chemical reactionssimultaneously.

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    TOPOLOGICAL RELATIONSHIP

    BETWEEN ORGANELLES

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    SPECIALISATION OF MEMBRANE

    FUNCTIONS

    Development of thylakoid vesicles in proplastids.

    In the process of differentiating into chloroplasts,specialized membrane patches form and pinch offfrom the inner membrane of the proplastid.

    The vesicles that pinch off form a newspecialized compartment, the thylakoid, thatharbors all of the chloroplast's photosyntheticmachinery.

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    EVOLUTIONARY ORIGINS

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    DNA molecule is attached to an invagination of theplasma membrane.

    Such an invagination could have rearranged to form

    an envelope around the DNA.

    This envelope is presumed to have eventuallypinched off completely from the plasma membrane,producing a nuclear compartment surrounded by adouble membrane.

    The nuclear compartment is topologicallyequivalent to the cytosol

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    MEMBRANE TRAFFICKING

    Flow of membrane material betweenendomembrane compartments and theplasmalemma

    Trafficking mainly by 3 mechanism- SIMPLE DIFFUSION- FACILITATED DIFFUSION

    - ACTIVE TRANSPORT

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    SIMPLE DIFFUSION

    Unassisted movement down the gradient

    Limited to small or nonpolar molecules.

    Ex:02 ,CO2 & lipids

    Exception: water molecules

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    FACILITATED DIFFUSION

    Protein mediated movement down thegradient

    Transport of large, polar molecules mediatedby carrier proteins

    Ex: Na+ , K , Ca+2 , Cl- etc.

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    ACTIVE TRANSPORT

    Protein-mediated movement Up the gradient

    May be powered by ATP hydrolysis, light

    energy, electrochemical potential of an iongradient

    Ex: ATP powered Na+/K+ pump.

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    VESICULAR TRANSPORT

    RER to cis Golgi

    Modified in Golgi (glycosylation,

    phosphorylation)

    Sorted at trans Golgi network into

    Lysosomal (endocytosis)

    Regulated (exocytosis)

    constitutive (exocytosis)

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    Vesicle formation and

    transport Capturing cargo molecules

    Vesicle coat

    - clathrin- COPI- COPII

    Vesicle docking

    -Surface markers called SNAREs , attach withtarget molecule SNAREs and fusion of bothmembrane occurs.

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    EXOCYTOSIS

    Cell releases intracellular molecules

    Molecules transportation by vesicles

    Vesicles fuses with plasma membrane

    5 steps involved

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    EXOCYTOSIS STEPS

    Vesicle trafficking

    Vesicle tethering

    Vesicle docking

    Vesicle priming

    Vesicle fusion

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    Final secretion by two process:

    - Constitutive Secretion- continuous secretion

    - Regulated Secretion

    - secreted in response to a specific signal

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    ENDOCYTOSIS

    Endocytosis is a process bywhich cells absorb molecules (such as proteins) byengulfing them.

    It is used by all cells of the body because mostsubstances important to them arelarge polar molecules that cannot pass throughthe hydrophobic plasma or cell membrane

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    Pathways for endocytic

    processes

    Phagocytosis

    Pinocytosis

    Receptor-mediated endocytosis

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    Phagocytosis

    Phagocytosis is the process of taking in particles such asbacteria, parasites, dead host cells, and cellular andforeign debris by a cell.

    Phagocytosis occurs after the foreign body or a bacterialcell comes near a plasma membrane of the cell

    For example, it has bound to molecules called"receptors" that are on the surface of the phagocyte.

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    Cells that uses

    PhagocytosisSeveral types of cells in the immune system engulf microorganismsvia phagocytosis.

    Neutrophils. Neutrophils are abundant in the blood, quicklyenter tissues, and phagocytize pathogens in acute inflammation.

    Macrophages. Macrophages are closely related to monocytes inthe blood. These longer-lived cells predominate in chronicinflammation. They also release some important inflammatoryparacrines. (See below.)

    Dendritic Cells. Phagocytosis in these cells is important for theelaboration of a specific immune response rather than for directly

    destroying the pathogens. B Lymphocytes. A small amount of phagocytosis in these cells is

    often necessary in order for them to develop into cells thatrelease antibodies

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    Phagocytosis in steps

    Phagocytosis begins with the neutrophil or macrophageflowing around the pathogen and engulfing it so that itwinds up enclosed in a phagosome (phagocytic vesicle).

    The next step is the fusion oflysosomes with thephagosome. The result is called a phagolysosome.

    Killing of microbes within a phagolysosome.

    oxygen radicles in membrane of phagolysosome

    antimicrobial proteins in lysosomes

    Hydrogen ion transport

    The final step is release of molecules and unwantedmolecules that comes insides the cell during ingestion

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    Pinocytosis

    It is the process of engulfing the liquid food.

    It requires energy in the form of ATP

    It is primarily used for absorption ofExtracellular Fluids.

    In contrast to phagocytosis, generates verysmall vesicles.

    It is non- specific

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    Pinocytosis

    In this, smallparticles arebrought into thecell, forming aninvagination, and

    then suspendedwithinsmall vesicles (pinocytotic vesicles) thatsubsequently fuse

    with lysosomes tohydrolyze, or tobreak down, theparticles

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    Receptor mediated

    endocytosis Also called clathrin-dependent endocytosis, It is a process by which cells internalize molecules

    (endocytosis) by the inward budding of plasmamembrane vesicles containing proteins with receptor sites

    specific to the molecules being internalized. Mechanism-After the binding of a ligand to plasma

    membrane-spanning receptors, a signal is sent through themembrane, leading to membrane coating, and formation of amembrane invagination. The receptor and its ligand are

    then opsonized in clathrin-coated vesicles. Once opsonized,the clathrin-coated vesicle uncoats (a pre-requisite for thevesicle to fuse with other membranes) and individual vesiclesfuse to form the early endosome

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    Function of RME

    Used for the specific uptake of certainsubstances required by the cell (examplesinclude LDL(low density lipo-proteins viathe LDL receptor or iron via transferrin).

    in the downregulation of transmembranesignal transduction. The activated receptor

    becomes internalised and is transported tolate endosomes and lysosomes fordegradation.

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    Transcytosis

    Transcytosis occurs as membrane-bound carriers

    selectively transport materials between one part

    of the cell and another in order to maintain

    unique environments on either side of the cell.

    Epithelial cells use transcytosis for immune

    defense, nutrient absorption, and plasma

    membrane biogenesis There are two types of transcytosis differing in

    mechanisms of vesicle formation and majorproteins

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    Clathrin-Mediated Transcytosis

    Clathrin, a protein located onboth apical and basal surfaces ofthe epithelial cells, lines thesevesicles. Clathrin-mediatedtranscytosis is a way for thesecells to sort through the cargoof molecules entering the cell asone of the destinations of thesevesicles is the Golgi. On thesurface of the cell membrane, apit forms from specific cell

    receptors that are coated byclathrin. The protein clathrinspurpose is to stabilize theforming vesicle after thereceptors have bound and beginto invaginate. Clathrin achievesthis by forming a rigid matrix ofan assembling of clathrinproteins, which can laterdisassemble after the vesicle has

    disassociated from the cellmembrane. Vesicles attach to theendoplasmic reticulum beforebeing "sorted" to either theapical or basal side of the cell.

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    Caveolae-Mediated Transcytosis

    Endothelial cells, specializedepithelium that line bloodvessels, utilize caveolae-mediated transcytosis.Caveolae are pits in theapical and basal membranesof all endothelial cells,named for their small caveshape. The major structural

    component of caveolae,shown in Figure 1, iscaveolin. These vesiclestransport cargo, usuallyfluid, from the apical tobasal or basal to apicalsurfaces of the cells. Thecaveolae can merge tocreate arrangements shown

    above (Figure 3), including atunnel or channel, in order tomove cargo to other side ofcell