Dumangcas
   Durante
 Odchimar
    Roa, S.
 These   nonmuscle cells lies just beneath the
    plasma membrane

 Arrangements      are less ordered, more
    labile, and transient unlike muscle
    cells/tissues.

 typically    restricted to a thin cortex

    ‘cortex’ is an active region of the cell,
    responsible for many cellular processes
    (e.g. the constriction of a single animal cell into two
    cells during cell division.)
1) Nucleating proteins

2) Monomer-sequestering proteins
3) End-blocking (capping) proteins
4) Monomer-polymerizing proteins

5) Actin filament-depolymerizing proteins

6) Cross-linking proteins

7) Filament-severing proteins
8) Membrane-binding proteins
   nucleation



                 Nucleating
                  protein
- prevent polymerizing
by isolation

          Monomer-
         sequestering
           proteins
- regulate the length of actin filaments by
    binding on an end and blocking a loss or
    gain of subunits



Capping
proteins
- promote the growth of actin filaments
- fragment actin filaments and promote
   depolymerization at the pointed end.
 promote   the formation of loose networks of
  filaments
 promote the bundling of actin filaments into
  tightly knit, parallel arrays
   bind to the side of an existing filament and
    break it in two.
- Link the actin filaments to the plasma
membrane indirectly, by means of
attachment to a peripheral membrane
protein                          Membrane-
                                   binding
                                   proteins
 Actin Polymerization as a Force-
  Generating Mechanism
 Cell Locomotion
  • Cells that Crawl over the Substratum
 AxonalOutgrowth
 Changes in Cell Shape during Embryonic
  Development
 How  is the bacterial cell able to induce the
 formation of actin filaments at a particular
 site on its surface?

 • Because Listeria contains a surface protein called
   ‘ActA’, it recruits and activates a number of host
   proteins that work together to direct the process of
   actin polymerization. (without the participation of
   myosin motors)
 Cells that Crawl over the Substratum
  • Aided by lamellipodia, it extend out from the
    cell as a broad, flattened, veil-like protrusion.
    Found by examining its leading edge.
Scanning electron micrograph of a mouse fibroblast
crawling over the surface of a culture dish.
 Cells that Crawl over the Substratum
  • Aided by lamellipodia, it extend out from the
    cell as a broad, flattened, veil-like protrusion.
    Found by examining its leading edge.
  • With these cells can move or analogically can
    walk.
shows the protrusion of the leading
  edge of the cell in the form of a
          lamellipodium.


       shows the adhesion
   of the lamellipodium to the
     substratum, to grip the
           substratum.


          shows
the movement of the bulk of the
        cell forward


              shows
  the rear of the cell has been
         pulled forward.
 Cells that Crawl over the Substratum
  • Aided by lamellipodia, it extend out from the
    cell as a broad, flattened, veil-like protrusion.
    Found by examining its leading edge.
  • With these cells can move or analogically can
    walk.
  • The protrusion of a lamellipodium is
    associated with the nucleation and
    polymerization of actin filaments and their
    association with various types of actin-binding
    proteins.
A proposed mechanism
for the movement of a cell in a directed manner
 Cells   that Crawl over the Substratum
  • Lamellipodial movement is a dynamic process.
  • As actin filament polymerization and branching
    continue at the very front edge of the
    lamellipodium, actin filaments are depolymerizing
    toward the rear of the lamellipodium.
Fluorescence            Drawing of a filamentous actin
micrographs of a fish   network of the lamellipodium
keratocyte              and the actin–myosin
                        interactions
 theexperiment of Ross Harrison provided a
 strong evidence that axons develop by a process
 of active outgrowth and elongation.

 Thetip of an elongating axon consists of a
 growth cone, which resembles a highly motile,
 crawling fibroblast and contains several types of
 locomotor protrusions, including a lamellipodium,
 microspikes, and filopodia.
 Changes in cell shape are brought about largely
 by changes in the orientation of cytoskeletal
 elements within the cells.

 One of the best examples of this phenomenon is
 seen in the early stages of the development of
 the nervous system.
nonmuscle motility

nonmuscle motility

  • 1.
    Dumangcas Durante Odchimar Roa, S.
  • 2.
     These nonmuscle cells lies just beneath the plasma membrane  Arrangements are less ordered, more labile, and transient unlike muscle cells/tissues.  typically restricted to a thin cortex  ‘cortex’ is an active region of the cell, responsible for many cellular processes (e.g. the constriction of a single animal cell into two cells during cell division.)
  • 3.
    1) Nucleating proteins 2)Monomer-sequestering proteins 3) End-blocking (capping) proteins 4) Monomer-polymerizing proteins 5) Actin filament-depolymerizing proteins 6) Cross-linking proteins 7) Filament-severing proteins 8) Membrane-binding proteins
  • 4.
    nucleation Nucleating protein
  • 5.
    - prevent polymerizing byisolation Monomer- sequestering proteins
  • 6.
    - regulate thelength of actin filaments by binding on an end and blocking a loss or gain of subunits Capping proteins
  • 7.
    - promote thegrowth of actin filaments
  • 8.
    - fragment actinfilaments and promote depolymerization at the pointed end.
  • 9.
     promote the formation of loose networks of filaments  promote the bundling of actin filaments into tightly knit, parallel arrays
  • 10.
    bind to the side of an existing filament and break it in two.
  • 11.
    - Link theactin filaments to the plasma membrane indirectly, by means of attachment to a peripheral membrane protein Membrane- binding proteins
  • 15.
     Actin Polymerizationas a Force- Generating Mechanism  Cell Locomotion • Cells that Crawl over the Substratum  AxonalOutgrowth  Changes in Cell Shape during Embryonic Development
  • 16.
     How is the bacterial cell able to induce the formation of actin filaments at a particular site on its surface? • Because Listeria contains a surface protein called ‘ActA’, it recruits and activates a number of host proteins that work together to direct the process of actin polymerization. (without the participation of myosin motors)
  • 18.
     Cells thatCrawl over the Substratum • Aided by lamellipodia, it extend out from the cell as a broad, flattened, veil-like protrusion. Found by examining its leading edge.
  • 19.
    Scanning electron micrographof a mouse fibroblast crawling over the surface of a culture dish.
  • 22.
     Cells thatCrawl over the Substratum • Aided by lamellipodia, it extend out from the cell as a broad, flattened, veil-like protrusion. Found by examining its leading edge. • With these cells can move or analogically can walk.
  • 23.
    shows the protrusionof the leading edge of the cell in the form of a lamellipodium. shows the adhesion of the lamellipodium to the substratum, to grip the substratum. shows the movement of the bulk of the cell forward shows the rear of the cell has been pulled forward.
  • 24.
     Cells thatCrawl over the Substratum • Aided by lamellipodia, it extend out from the cell as a broad, flattened, veil-like protrusion. Found by examining its leading edge. • With these cells can move or analogically can walk. • The protrusion of a lamellipodium is associated with the nucleation and polymerization of actin filaments and their association with various types of actin-binding proteins.
  • 25.
    A proposed mechanism forthe movement of a cell in a directed manner
  • 26.
     Cells that Crawl over the Substratum • Lamellipodial movement is a dynamic process. • As actin filament polymerization and branching continue at the very front edge of the lamellipodium, actin filaments are depolymerizing toward the rear of the lamellipodium.
  • 29.
    Fluorescence Drawing of a filamentous actin micrographs of a fish network of the lamellipodium keratocyte and the actin–myosin interactions
  • 31.
     theexperiment ofRoss Harrison provided a strong evidence that axons develop by a process of active outgrowth and elongation.  Thetip of an elongating axon consists of a growth cone, which resembles a highly motile, crawling fibroblast and contains several types of locomotor protrusions, including a lamellipodium, microspikes, and filopodia.
  • 34.
     Changes incell shape are brought about largely by changes in the orientation of cytoskeletal elements within the cells.  One of the best examples of this phenomenon is seen in the early stages of the development of the nervous system.

Editor's Notes

  • #3 Nonmusclemotility depends on actin,
  • #4  ACTIN BINDING PROTEINS ARE THE factorsthat govern the rates of assembly, numbers, lengths, and spatial patterns of actin filaments.
  • #18 (a) Fluorescence micrograph of a portion of a cell infected with the bacteriumL. monocytogenes. The bacteria appear as red-stained objects justin front of the green-stained filamentous actin tails. (b) Electron micrographof a cell infected with the same bacterium as in a, showing theactin filaments that form behind the bacterial cell and push it throughthe cytoplasm. The actin filaments have a bristly appearance becausethey have been decorated with myosin heads. Bar at the upper left,0.1 m.
  • #20 Figure 9.68 shows a single fibroblast that was in theprocess of moving toward the lower right corner of the field when it was prepared for microscopy.Cell locomotion, as exhibited by the fibroblast in Figure 9.68, shares properties with other types of locomotion, for example, walking animals (with legs).
  • #24 The repetitive sequence of activities that occurs as a cellcrawls over the substratum
  • #29 Distribution of traction forces within a migratingfibroblast.
  • #30 Left photo - Fluorescence micrographs of a fish keratocyte moving over a culture dish by means of a broad, flattened lamellipodium.Right- A schematic drawing depicting the filamentous actin network of the lamellipodium and the actin–myosin interactions toward the rear of the lamellipodium.