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CELL JUNCTIONS I-Occluding junctions II-Anchoring junctions III-Channel-forming junctions IV-Signal-relaying junctions Plasma membrane specializations, called cell junctions, mediate between neighbouring cells and between cells and the basal lamina. Cell junctions are particularly abundant in epithelia. Cell junctions form barriers that inhibit the movement of water and solutes. Microvillus Tight junction Adherens junctions Desmosomes Gap junction Hemidesmosome Cell-cell and cell-matrix junctions Basal Lamina I-Tight junction=Zonula occludens =Occluding junction Tight junctions prevent diffusion of plasma membrane proteins and glycolipids. Tight junctions form a barrier that seals off body cavities from the blood. Freeze-fracture images revealed that tight junction consist of integral membrane proteins : Occludin and Claudins Endothelial cells in most regions of the brain and spinal cord are joined by tight junctions. The blood-brain barrier separates the blood from the interstitial fluid. II. ANCHORING JUNCTIONS 1.ADHERENS JUNCTIONS and DESMOSOMES hold cells and are formed by adhesion proteins of the cadherin family. 2.FOCAL ADHESIONS(Actin-linked cell- matrix adhesion) and HEMIDESMOSOMES bind cells to the extracellular matrix and are formed by adhesion proteins of the integrin family. Actin filament attachment sites 1.Cell-cell junction (ADHERENS JUNCTIONS) 2.Cell-matrix junctions (FOCAL ADHESIONS) Intermediate filament attachment sites 1.Cell-cell junctions (DESMOSOMES) 2.Cell-matrix junctions (HEMIDESMOSOMES) Adherens junction maintains the physical integrity of the epithelium. These junctions form adhesion belts between epithelial cells. 1. Cell membrane α-catenin 2. Cell membrane Cadherin p120 β-catenin Vinculin α-Actinin Actin filament Outside of cell Adherens junctions Focal adhesions bind cells on the extracellular matrix through integrins that link to actin filaments. Actin-linked cell-matrix adhesion forms by integrins. Focal contacts faciliate certain types of cellular movement. Desmosomes are button like points between adjacent cells The particular type of intermediate filaments attached to the desmosomes: keratin filaments in most epithelial cells, desmin filaments in heart and muscle cells Desmosomes are found in many tissues especially abundant in skin, heart, muscle, the neck of the uterus. Desmosomes prevent mechanical stress Desmosome 1. Cell membrane 2. Cell Membrane Desmoglein Desmoplakin Intermediate filaments Plakoglobulin Desmocollin Plakophilin Outside of cell Two types of cadherins(desmoglein and desmocolin) bind via anchor protein to intermediate filaments. Cytoplasmic plaque (desmoplakin,plakoglobin and plakophilin) link the cadherins. The importance of desmosome is demonstrated by some forms of the fatal skin autoimmune disease PEMPHİGUS. Desmoglein 1------Pemphigus foliaceus Desmoglein 3------Pemphigus vulgaris Hemidesmosomes Hemidesmosomes connect an epithelial cell to the basal lamina. They act as rivets to distribute tensile. Hemidesmosomes have a dense plaque on the cytoplasmic surface that anchors of intermediate filaments. Integrin (α6β4) and type XVII collagen (also called BPAG2) attach to the basal lamina. A disease of hemidesmosomal molecules: Bullous pemphigoid autoantibodies attack type XVII collagen. III-Channel-forming junctions 1-Gap junctions 2-Plasmodesmata (plants only) 1- Gap junctions Most cells are in communication with their neighbours via gap junction. Gap junctions serve as direct connections between adjacent cells. Each gap junction can contain a cluster of many thousands of connexons. Connexins are transmembrane proteins, six of which assemble to form a channel, a connexon. Gap junction channels allow to pass ions, second messengers and metabolites. The sharing of metabolites and ions provides a mechanism for coordinating the activities of cells. The permeability of gap junctions is regulated by the cytosolic pH or the cytosolic concentration of free Ca2+ Gap junction communication can be regulated by extracellular signals. Gap junctions are usually present low density in most adult epithelia, but are found in large numbers during embryogenesis. Electrical synapses depend on gap junction channels. In the neocortex and thalamus and some other parts of the brain electrical synapses are common. Mutations in connexin genes cause disease Recessive mutations in the connexin-26 gene are the most common causes of inherited human deafness. Mutation in the connexin-32 cause CharcotMarie-Tooth disease, which is marked by progressive degeneration of peripheral nerves. 2-Plasmodesmata Adjacent plant cells communicate with each other through cytoplasmic connections called plasmodesmata (singular plasmodesma). A plasmodesma contains a fine tubular structure, the desmotubule, derived from smooth endoplasmic reticulum. IV-Signal-relaying junctions Chemical synapses (in the nervous system) A chemical synapse The arrival of an impulse at the terminus of a neuron triggers synaptic vesicles to fuse with membrane, releasing neurotransmitter. The released neurotransmitter in the synaptic cleft binds to a receptor on the postsynaptic membrane to pass information. a- Resting Mitochondrion Presynaptic terminal of the cell Transmittergated ion channel :: :: Neurorotransmitter Synaptic cleft b- Active chemical synapse :: :: :: :: : : Postsynaptic cell Chemical synapses :: KAYNAKLAR 1-Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P. : Molecular Biology of The Cell. Fifth Edition Garland Science Taylor & Francis Group New York 2008. 2-Pollard T.D. and Earnshaw W.C. : Cell Biology. Second Edition. Saunders Elsevier USA 2008. 3-Lodish H, Berk A, Kaiser C A, Krieger M, Scott M P, Bretscher A, Ploegh H, Matsudaira P: Molecular Cell Biology. Sixth Edition. W.H. Freeman and Company New York 2008. 4-Weaver R.F. Molecular Biology. Third EditionMcGraw-Hill Higher Education, New York 2005. 5-Cooper G.M. and Hausman R.E. : The Cell: A molecular Approach 5th Edition. ASM Press Sinauer Associates Inc. USA 2009. 6-Epstein R.J. : Human Molecular Biology. Cambridge University Press UK 2003. 7-Kierszenbaum A. L. and Tres L.L.: Histology and Cell Biology: An Introduction to Pathology. Third Edition. Mosby Elsevier USA 2012.