Interactions Between Cells
  and Their Environment
Introduction
Cells don’t exist alone.
Cells interact with extracellular material
 to form defined tissues.
These interactions are crucial to the
 formation of epithelial tissue and
 connective tissue, which are crucial for
 various cellular activities.
Introduction (Cont.)
Cell migration, cell growth, cell
 differentiation, 3-D organization of
 tissues and organs that emerges during
 embryonic development.
Overview of cell organization into
             tissues
     • Click to edit Master text styles
       – Second level
       – Third level
          • Fourth level
              – Fifth level
7.1 The Extracellular Space (1)
The glycocalyx (cell
 coat) is formed from
 carbohydrate
 projections form the
 plasma membrane.
Outer surface of the
 plasma membrane
7.1 The Extracellular Space (cont.)
Gycocalyx
  Mediate cell-cell and cell-substratum
   interactions
  Provide mechanical protection to cells
  Barrier to particles moving toward
   plasma membrane
  Bind important regulatory factors
The Extracellular Space (cont.)
The extracellular matrix (ECM) is an
 organized network of proteins and
 polysaccharides beyond the plasma
 membrane.
 “Glue” that holds cells together
 It often plays a regulatory role in
   determining shape and activities of
   the cell.
Organization of the ECM
The Extracellular Space (cont.)
 ECM (continued)
   The basement membrane (basal lamina) is
    a continuous sheet that underlies epithelial
    tissue and surrounds blood vessels.
   Helps maintain cells attached.
   Serves as substratum for cell migration.
   Forms a barrier to macromolecules.
The basement membrane
Extracellular matrix
Gel-like “ground substance”
Primarily made of polysaccharides
  Gylycosaminoglycans (GAGs)
  proteoglycans
Fibrous proteins
  Collagen, laminin, elastin, fibronectin
  Structure and adhesive functions
The Extracellular Space (cont.)
 Collagens – fibrous glycoproteins found only
  in the ECM.
   Collagen is the most abundant protein in
     the human body.
   Provide high tensile strength.
   Each collagen is restricted to particular
     locations in the body.
   All collagens are a trimer of polypeptide
     chains (α chains) and 3 polypeptide chains
     are wound around each other.
The structure of collagen I
Major types of collagen
 Type I collagen
   The chief component of tendons,
   ligaments, and bones.
 Type II collagen
  Represents more than 50% of the protein in
   cartilage and is the major component of the
   vitreous body of the eye.
   It is also used to build the notochord of
   vertebrate embryos.
 Type III collagen
   Strengthens the walls of hollow structures like
   arteries, the intestine, and the uterus.
 Type IV collagen
   Forms the basal lamina of epithelia. (The basal
   lamina is often called the basement membrane.)A
   meshwork of Type IV collagens provides the filter
   for the blood capillaries and the glomeruli of the
   kidneys.
The Extracellular Space (cont.)
 Collagens (continued)
   Provide the insoluble
    framework that
    determines
    mechanical
    properties of the
    matrix.
   Abnormalities in
    collagen formation
    lead to serious
    disorders.
The Extracellular Space (cont.)
Collagens type I, II, III are fibrillar
 collagens
  Assemble into rigid, cable-like fibrils
   (assembles like fibers)
  Example: tendon – collagens are
   parallel to tendons thus parallel to
   pulling actions
The Extracellular Space (cont.)
Abnormalities in
 fibrillar collagens
 formation can lead to
 serious disorders
Mutation in in genes
 encoding type I
 collagen can produce
 osteogenesis imperfecta
  Extremely fragile bones,
The Extracellular Space (cont.)
 Mutation in genes encoding
  type II alter the properties of
  cartilage tissue causing
  dwarfism and skeletal
  deformities
 Mutations in other collagens
  genes that are related in
  collagen matrix structure
  can lead to Ehler-Danlos
  sydromes
The Extracellular Space (cont.)
Not all collagens form
 fibrils.
Collagen type IV is
 non-fibrillar, and is
 restricted to the
 basement membrane.
The Extracellular Space (cont.)
 Mutations in type IV
  collagen genes causes
  Alport syndrome
  A kidney disease in
   which glomerular
   basement
   membrane is
   disrupted
The Extracellular Space (cont.)
Proteoglycans – protein-polysaccharide
 complex, with a core protein attached to
 glycosaminoglycans (GAGs).
GAGs
  Have a repeating disaccharide
   structure.
  Negatively charged
The Extracellular Space (cont.)
Negatively charged GAGs attract lots of
 cations, which in turn attract water
 forming a porous, hydrated gel.
Function:
to be able to withstand compressional
 forces through hydration and swelling
 pressure (turgor) to the tissue
• Click to edit Master text styles
  – Second level
  – Third level
     • Fourth level
         – Fifth level
Structure of a proteoglycan complex
Structure of a proteoglycan complex
The Extracellular Space (cont.)
Forms complement to collagen molecule
Together, they give cartilage and other
 extracellular matrices strength and
 resistance to deformation
Example: ECM of bones
  Collagen + Proteoglycans + calcium
   sulfate ions = bones
GAG chains of proteoglycans also act as
The Extracellular Space (cont.)
 Fibronectin (Fn)
 Multiple binding domains
  Complex proteins that binds to multiple
   substrates
 Helps cells attach to matrix
 Fn has binding sites for other components of
  the ECM.
 RGD
Structure of fibronectin
The Extracellular Space (cont.)
 Fibronectin (FN) is involved in many cellular
  processes, including tissue repair,
  embryogenesis, blood clotting, and cell
  migration/adhesion.
 Fibronectin sometimes serves as a general cell
  adhesion molecule
 FN also can serve to organize cellular
The Extracellular Space (cont.)
 Laminins – extracellular
  glycoproteins consisting
  of three polypeptide
  chains linked by disulfide
  bonds.
   Help cell migration
     during development.
   Components of
     basement membranes.
The Extracellular Space (cont.)
 Dynamic Properties
  The ECM can be stretched during tension.
  ECM materials degraded by matrix
    metalloproteinases (MMPs).
  MMPs possibly involved in tissue remodeling,
    embryonic cell migration, wound healing , and
    formation of blood vessels.
  Excessive MMPs causes arthritis, hepatitis,
    atherosclerosis, tooth and gum disease and
    tumor progression
7.2 Interactions of Cells with
         Extracellular Materials
 Integrins – family of membrane proteins
  composed of heterodimers with α and ß
  subunits.
   Have a major role in integrating
     extracellular and intracellular
     environments.
   Another role is adhesion of cells to their
     substratum or other cells.
Model of integrin activation
Interactions of Cells with Extracellular
              Materials (cont.)
 Integrins (continued)
   Linkage between
     integrins and their
     ligands mediates
     adhesion between
     cells and their
     environment.
   Binding of proteins to
     integrins is facilitated
     by tripeptide RGD.
Interactions of Cells with Extracellular
           Materials (cont.)
Integrins (continued)
  Cytoplasmic domains of integrins
   contain binding sites for a variety of
   cytoplasmic proteins.
  Integrins make the connection
   between the ECM and the
   cytoskeleton.
Blood clotting
 Injury conformational
  change in platelets’
  integrin activation
     inc. fibrinogen
  affinity aggregation of
  platelets


Synthetic RGD peptides
-> inhibit blood clot
Interactions of Cells with Extracellular
           Materials (cont.)
Focal adhesions are found at the cell
 membrane where the cytoskeleton
 interacts with proteins of the
 extracellular matrix
Focal adhesions – scattered, discrete
 sites for cell adhesion to their
 substratum in vitro.
  They may act as a type of sensory
    structure.
 The clustering of integrins at these sites
  attracts a large complex of proteins and
  initiates intracellular regulatory processes, by
  which such events as cell migration and
  anchorage-dependent differentiation are
  controlled.
 Focal adhesion kinase (FAK) is a protein
  tyrosine kinase which is recruited at an early
  stage to focal adhesions and which mediates
  many of the downstream responses.
Focal adhesions
Focal adhesions
Interactions of Cells with
   Extracellular Materials (cont.)
Hemidesmosomes are cell-substratum
 adhesion sites that connect the
 extracellular matrix to the keratin
 cytoskeleton
 basal attachments of epithelial cells to
 the basement membrane in vivo.
  Contain a dense plaque with filaments
   consisting of keratin.
form rivet-like links between cytoskeleton and
extracellular matrix components such as the basal
          lamina that underlie epithelia
Hemidesmosomes
7.3 Interaction of Cells with Other
               Cells
 Cells have surface-
  recognition sites that
  maintain
  organization
Interaction of Cells with Other Cells
               (cont.)
Selectins – family
 of integral
 membrane
 glycoproteins that
 bind to sugars on
 the surface of
 cells.
Interaction of Cells with Other Cells
               (cont.)
 Selectins (continued)
  Contain a small cytoplasmic domain, a
   single membrane-spanning domain, and a
   large extracellular segment.
  Three types:
  E-selectin – on endothelial cells.
  P-selectin – on platelets and endothelial
   cells.
Interaction of Cells with Other Cells
                 (cont.)
 Immunoglobulin
  superfamily (IgSF) –
  most proteins are
  involved in immune
  functions.
  Most IgSF molecules
   mediate interaction
   of lymphocytes with
   cells required or
   immune response.
TIGHT JUNCTIONS

    located at the apical end of the
    junctional complex between adjacent
    epithelial cells

    sites where integral proteins of two
    adjacent membranes meet

    block the diffusion of solutes and
    water

    “fences”
 Interactions Between Cells and Their Environment

    claudin – major structural component

    claudin – 16
    − expressed in TAL

    claudin – 1
    − prevents water loss

    blood-brain barrier
    − prevents drugs from entering CNS
GAP JUNCTIONS

    sites for intercellular communication

    plasma membranes come very close,
    but no contact

    composed of connexin subunit:
    connexon

    allow molecules less than 1000
    daltons

    relatively nonselective

    channel closure is triggered by
    phosphorylation of connexin

    have a potential to integrate individual
    cells into functional unit

    allow cells to share metabolites

    connexons
     − differ in conductance, permeability,
       and regulation
     − promote or prevent communication
     − mutation resulting to disorder might
       cause defects

    tunneling nanotubules
     − conducting cell surface proteins
 Interactions Between Cells and Their Environment
PLASMODESMATA

    cytoplasmic channels that pass
    through cell walls

    desmotubule

    sites of cell to cell communication

    capable of dilation
 Interactions Between Cells and Their Environment
CELL WALLS


    bacteria, fungi, plants

    gives polyhedral shape

    “skeleton”

    source of signal

    cellulose
     − fibrous component of cell wall

    protiens and pectin
     − provide matrix

    cellulose
    −   cellulose synthase
    −   organized into rod-like microfibrils
        
            provide rigidity
        
            resistance to tensile forces
    −   polymerized at cell surface

    matrix
    −   synthesized in the cytoplasm
    −   three types of macromolecules

    hemicelluloses
    − bind to the surfaces of cellulose
      microfibrils

    pectins
    − holds water

    proteins
    − expansins – cell growth
    − elongation
CELL WALLS

    thin cell plate

    provide suporrt

    primary walls

    secondary walls

    lignin
     − structural support
     − in xylem, move water through the
       plant
 Interactions Between Cells and Their Environment
 Interactions Between Cells and Their Environment
 Interactions Between Cells and Their Environment
 Interactions Between Cells and Their Environment
 Interactions Between Cells and Their Environment
 Interactions Between Cells and Their Environment

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Interactions Between Cells and Their Environment

  • 1. Interactions Between Cells and Their Environment
  • 2. Introduction Cells don’t exist alone. Cells interact with extracellular material to form defined tissues. These interactions are crucial to the formation of epithelial tissue and connective tissue, which are crucial for various cellular activities.
  • 3. Introduction (Cont.) Cell migration, cell growth, cell differentiation, 3-D organization of tissues and organs that emerges during embryonic development.
  • 4. Overview of cell organization into tissues • Click to edit Master text styles – Second level – Third level • Fourth level – Fifth level
  • 5. 7.1 The Extracellular Space (1) The glycocalyx (cell coat) is formed from carbohydrate projections form the plasma membrane. Outer surface of the plasma membrane
  • 6. 7.1 The Extracellular Space (cont.) Gycocalyx Mediate cell-cell and cell-substratum interactions Provide mechanical protection to cells Barrier to particles moving toward plasma membrane Bind important regulatory factors
  • 7. The Extracellular Space (cont.) The extracellular matrix (ECM) is an organized network of proteins and polysaccharides beyond the plasma membrane. “Glue” that holds cells together It often plays a regulatory role in determining shape and activities of the cell.
  • 9. The Extracellular Space (cont.)  ECM (continued) The basement membrane (basal lamina) is a continuous sheet that underlies epithelial tissue and surrounds blood vessels. Helps maintain cells attached. Serves as substratum for cell migration. Forms a barrier to macromolecules.
  • 11. Extracellular matrix Gel-like “ground substance” Primarily made of polysaccharides Gylycosaminoglycans (GAGs) proteoglycans Fibrous proteins Collagen, laminin, elastin, fibronectin Structure and adhesive functions
  • 12. The Extracellular Space (cont.)  Collagens – fibrous glycoproteins found only in the ECM. Collagen is the most abundant protein in the human body. Provide high tensile strength. Each collagen is restricted to particular locations in the body. All collagens are a trimer of polypeptide chains (α chains) and 3 polypeptide chains are wound around each other.
  • 13. The structure of collagen I
  • 14. Major types of collagen  Type I collagen  The chief component of tendons, ligaments, and bones.  Type II collagen Represents more than 50% of the protein in cartilage and is the major component of the vitreous body of the eye.  It is also used to build the notochord of vertebrate embryos.
  • 15.  Type III collagen  Strengthens the walls of hollow structures like arteries, the intestine, and the uterus.  Type IV collagen  Forms the basal lamina of epithelia. (The basal lamina is often called the basement membrane.)A meshwork of Type IV collagens provides the filter for the blood capillaries and the glomeruli of the kidneys.
  • 16. The Extracellular Space (cont.)  Collagens (continued) Provide the insoluble framework that determines mechanical properties of the matrix. Abnormalities in collagen formation lead to serious disorders.
  • 17. The Extracellular Space (cont.) Collagens type I, II, III are fibrillar collagens Assemble into rigid, cable-like fibrils (assembles like fibers) Example: tendon – collagens are parallel to tendons thus parallel to pulling actions
  • 18. The Extracellular Space (cont.) Abnormalities in fibrillar collagens formation can lead to serious disorders Mutation in in genes encoding type I collagen can produce osteogenesis imperfecta Extremely fragile bones,
  • 19. The Extracellular Space (cont.)  Mutation in genes encoding type II alter the properties of cartilage tissue causing dwarfism and skeletal deformities  Mutations in other collagens genes that are related in collagen matrix structure can lead to Ehler-Danlos sydromes
  • 20. The Extracellular Space (cont.) Not all collagens form fibrils. Collagen type IV is non-fibrillar, and is restricted to the basement membrane.
  • 21. The Extracellular Space (cont.)  Mutations in type IV collagen genes causes Alport syndrome A kidney disease in which glomerular basement membrane is disrupted
  • 22. The Extracellular Space (cont.) Proteoglycans – protein-polysaccharide complex, with a core protein attached to glycosaminoglycans (GAGs). GAGs Have a repeating disaccharide structure. Negatively charged
  • 23. The Extracellular Space (cont.) Negatively charged GAGs attract lots of cations, which in turn attract water forming a porous, hydrated gel. Function: to be able to withstand compressional forces through hydration and swelling pressure (turgor) to the tissue
  • 24. • Click to edit Master text styles – Second level – Third level • Fourth level – Fifth level
  • 25. Structure of a proteoglycan complex
  • 26. Structure of a proteoglycan complex
  • 27. The Extracellular Space (cont.) Forms complement to collagen molecule Together, they give cartilage and other extracellular matrices strength and resistance to deformation Example: ECM of bones Collagen + Proteoglycans + calcium sulfate ions = bones GAG chains of proteoglycans also act as
  • 28. The Extracellular Space (cont.)  Fibronectin (Fn)  Multiple binding domains Complex proteins that binds to multiple substrates  Helps cells attach to matrix  Fn has binding sites for other components of the ECM.  RGD
  • 30. The Extracellular Space (cont.)  Fibronectin (FN) is involved in many cellular processes, including tissue repair, embryogenesis, blood clotting, and cell migration/adhesion.  Fibronectin sometimes serves as a general cell adhesion molecule  FN also can serve to organize cellular
  • 31. The Extracellular Space (cont.)  Laminins – extracellular glycoproteins consisting of three polypeptide chains linked by disulfide bonds. Help cell migration during development. Components of basement membranes.
  • 32. The Extracellular Space (cont.)  Dynamic Properties The ECM can be stretched during tension. ECM materials degraded by matrix metalloproteinases (MMPs). MMPs possibly involved in tissue remodeling, embryonic cell migration, wound healing , and formation of blood vessels. Excessive MMPs causes arthritis, hepatitis, atherosclerosis, tooth and gum disease and tumor progression
  • 33. 7.2 Interactions of Cells with Extracellular Materials  Integrins – family of membrane proteins composed of heterodimers with α and ß subunits. Have a major role in integrating extracellular and intracellular environments. Another role is adhesion of cells to their substratum or other cells.
  • 34. Model of integrin activation
  • 35. Interactions of Cells with Extracellular Materials (cont.)  Integrins (continued) Linkage between integrins and their ligands mediates adhesion between cells and their environment. Binding of proteins to integrins is facilitated by tripeptide RGD.
  • 36. Interactions of Cells with Extracellular Materials (cont.) Integrins (continued) Cytoplasmic domains of integrins contain binding sites for a variety of cytoplasmic proteins. Integrins make the connection between the ECM and the cytoskeleton.
  • 37. Blood clotting  Injury conformational change in platelets’ integrin activation inc. fibrinogen affinity aggregation of platelets Synthetic RGD peptides -> inhibit blood clot
  • 38. Interactions of Cells with Extracellular Materials (cont.) Focal adhesions are found at the cell membrane where the cytoskeleton interacts with proteins of the extracellular matrix Focal adhesions – scattered, discrete sites for cell adhesion to their substratum in vitro. They may act as a type of sensory structure.
  • 39.  The clustering of integrins at these sites attracts a large complex of proteins and initiates intracellular regulatory processes, by which such events as cell migration and anchorage-dependent differentiation are controlled.  Focal adhesion kinase (FAK) is a protein tyrosine kinase which is recruited at an early stage to focal adhesions and which mediates many of the downstream responses.
  • 42. Interactions of Cells with Extracellular Materials (cont.) Hemidesmosomes are cell-substratum adhesion sites that connect the extracellular matrix to the keratin cytoskeleton  basal attachments of epithelial cells to the basement membrane in vivo. Contain a dense plaque with filaments consisting of keratin.
  • 43. form rivet-like links between cytoskeleton and extracellular matrix components such as the basal lamina that underlie epithelia
  • 45. 7.3 Interaction of Cells with Other Cells  Cells have surface- recognition sites that maintain organization
  • 46. Interaction of Cells with Other Cells (cont.) Selectins – family of integral membrane glycoproteins that bind to sugars on the surface of cells.
  • 47. Interaction of Cells with Other Cells (cont.)  Selectins (continued) Contain a small cytoplasmic domain, a single membrane-spanning domain, and a large extracellular segment. Three types: E-selectin – on endothelial cells. P-selectin – on platelets and endothelial cells.
  • 48. Interaction of Cells with Other Cells (cont.)  Immunoglobulin superfamily (IgSF) – most proteins are involved in immune functions. Most IgSF molecules mediate interaction of lymphocytes with cells required or immune response.
  • 49. TIGHT JUNCTIONS  located at the apical end of the junctional complex between adjacent epithelial cells  sites where integral proteins of two adjacent membranes meet  block the diffusion of solutes and water  “fences”
  • 51. claudin – major structural component  claudin – 16 − expressed in TAL  claudin – 1 − prevents water loss  blood-brain barrier − prevents drugs from entering CNS
  • 52. GAP JUNCTIONS  sites for intercellular communication  plasma membranes come very close, but no contact  composed of connexin subunit: connexon  allow molecules less than 1000 daltons  relatively nonselective
  • 53. channel closure is triggered by phosphorylation of connexin  have a potential to integrate individual cells into functional unit  allow cells to share metabolites
  • 54. connexons − differ in conductance, permeability, and regulation − promote or prevent communication − mutation resulting to disorder might cause defects  tunneling nanotubules − conducting cell surface proteins
  • 56. PLASMODESMATA  cytoplasmic channels that pass through cell walls  desmotubule  sites of cell to cell communication  capable of dilation
  • 58. CELL WALLS  bacteria, fungi, plants  gives polyhedral shape  “skeleton”  source of signal  cellulose − fibrous component of cell wall  protiens and pectin − provide matrix
  • 59. cellulose − cellulose synthase − organized into rod-like microfibrils  provide rigidity  resistance to tensile forces − polymerized at cell surface  matrix − synthesized in the cytoplasm − three types of macromolecules
  • 60. hemicelluloses − bind to the surfaces of cellulose microfibrils  pectins − holds water  proteins − expansins – cell growth − elongation
  • 61. CELL WALLS  thin cell plate  provide suporrt  primary walls  secondary walls  lignin − structural support − in xylem, move water through the plant