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I. Cytoplasm
A. Plasma membrane B. Mitochondria C. Ribosomes D. Endoplasmic reticulum 1. Rough 2. Smooth E. Golgi apparatus F. Lysosomes G. Cytoskeleton
II. Nucleus
A. Nuclear Envelope B. Chromatin C. Nucleolus D. Nuclear matrix
2002 by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter.
Figure 21. The ultrastructure and molecular organization (right) of the cell membrane. The dark lines at left represent the two dense layers observed in the electron microscope; these are caused by the deposit of osmium in the hydrophilic portions of the phospholipid molecules.
2002 by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter.
Figure 1114. Electron micrograph of a transverse section of a continuous capillary. Note the nucleus (N) and the junctions between neighboring cells (arrowheads). Numerous pinocytotic vesicles are evident (small arrows).
C. Ribosomes
Characteristics
Ribosomes
are very basophilic, stain with hematoxylin , toluidine blue Found in clusters called polyribosomes that are held together by a strand of RNA.
Polyribosomes
mRNA
Ribosome
Ribosome function
Translation of mRNA into protein Free polyribosomes- synthesize proteins used in the cytoplasm Polyribosomes attached to the ER- used to synthesize
Secreted proteins Integral membrane proteins Lysosomal proteins
2002 by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter.
Ribosome-two thirds RNA, one third protein Each ribosome has three binding sites for tRNA, and a binding site for mRNA
2002 by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter.
Endoplasmic Reticulum
Segregation of newly synthesized proteins from the cytoplasm Glycosylation of certain proteins Lipid synthesis
RER structure
RER
Contains
Functions
Synthesize
Figure 219. The ultrastructure of a cell that synthesizes (but does not secrete) proteins on free polyribosomes (A); a cell that synthesizes, segregates, and stores proteins in organelles (B); a cell that synthesizes, segregates, and directly exports proteins (C); and a cell that synthesizes, segregates, stores in supranuclear granules, and exports proteins (D).
SER
Structure
Lacks
Function
Detoxification
Golgi apparatus
Posttranslational processing including glycosylation, phosphorylation, proteolysis Packing and concentration of secretory granules
Apical
Basal
Lysosomes
Membrane bound vesicles that contain hydrolytic enzymes for digestion Heterophagy
Digestion
of extracellular material
Autophagy digestion of intracellular organelles Review Table 2-3 for clinical correlations
Eg.
Figure 227. Current concepts of the functions of lysosomes. Synthesis occurs in the rough endoplasmic reticulum (RER), and the enzymes are packaged in the Golgi complex. Note the heterophagosomes, in which bacteria are being destroyed, and the autophagosomes, with RER and mitochondria in the process of digestion. Heterophagosomes and autophagosomes are secondary lysosomes. The result of their digestion can be excreted, but sometimes the secondary lysosome creates a residual body, containing remnants of undigested molecules. In some cells, such as osteoclasts, the lysosomal enzymes are secreted to the extracellular environment. Nu, nucleolus.
Cytoskeleton
cell shape Cell movement (diapedesis) Cytoplasm movement (ie. transport of secretory granules)
Microtubules
microtubules triplets
Microfilaments
Eg. Actin, @ 6-8 nm thick Most cells have actin to some extent
Intermediate filaments
Table 2-4 @ 10 nm diameter Lamin, nuclear envelope protein GFAP, glial fibrillary acidic protein, glial cells (astrocytes)
10 nm
2002 by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter.
Nuclear envelope
Invisible with light microscope Nuclear pores- areas of fusion between two sheaths of nuclear envelope
<
RER
Nuclear pore
Nuclear envelope
Perinuclear space
Figure 35. Illustration to show the structure, the localization, and the relationship of the nuclear lamina with chromosomes. The drawing also shows that the nuclear pore complex is made of 2 protein rings in an octagonal organization. From the cytoplasmic ring, long filaments penetrate the cytosol, and from the intranuclear ring arise filaments that constitute a basketlike structure. The presence of the central cylindrical granule in the nuclear pore is not universally accepted.
Figure 36. Electron micrographs of nuclei showing their envelopes composed of 2 membranes and the nuclear pores (arrows). The two upper pictures are of transverse sections; the bottom is of a tangential section. Chromatin, frequently condensed below the nuclear envelope, is not usually seen in the pore regions. x80,000.
Figure 37. Electron micrograph obtained by cryofracture of a rat intestine cell, showing the two components of the nuclear envelope and the nuclear pores. (Courtesy of P Pinto da Silva.)
2002 by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter.
Nuclear lamina
Fibrous, between nuclear envelope and chromatin Composed of intermediate filamentslamins Pulls nucleus back together during telophase
Chromatin
Heterochromatin- very e- dense, basophilic Euchromatin- very light staining Can be used to determine cell activity
Light
Figure 39. Schematic representation of a nucleosome. This structure consists of a core of 4 types of histones (2 copies of each) H2A, H2B, H3, and H4and one molecule of H1 or H5 located outside the DNA filament.
Figure 310. The orders of chromatin packing believed to exist in the metaphase chromosome. Starting at the top, the 2-nm DNA double helix is shown; next is the association of DNA with histones to form filaments of nucleosomes of 11 nm and 30 nm. Through further condensation, filaments with diameters of 300 nm and 700 nm are formed. Finally, the bottom drawing shows a metaphase chromosome, which exhibits the maximum packing of DNA.
Nucleolus
Spherical, lots of RNA and protein Very basophilic Site of ribosome synthesis
2002 by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter.
Figure 312. Human karyotype preparation made by means of a banding technique. Each chromosome has a particular pattern of banding that facilitates its identification and also the relationship of the banding pattern to genetic anomalies. The chromosomes are grouped in numbered pairs according to their morphologic characteristics.
Figure 316. Photomicrograph of cultured cells to show cell division. Picrosirius-hematoxylin stain. Medium magnification. A: Interphase nuclei. Note the chromatin and nucleoli inside each nucleus. B: Prophase. No distinct nuclear envelope, no nucleoli. Condensed chromosomes. C: Metaphase. The chromosomes are located in a plate at the cell equator. D: Late anaphase. The chromosomes are located in both cell poles, to distribute the DNA equally between the daughter cells.
Figure 318. Electron micrograph of a section of a rooster spermatocyte in metaphase. The figure shows the two centrioles in each pole, the mitotic spindle formed by microtubules, and the chromosomes in the equatorial plane. The arrows show the insertion of microtubules in the centromeres. Reduced from x19,000. (Courtesy of R McIntosh.)
Interphase
G1- RNA, protein synthesis S- DNA synthesis G2-cell growth, synthesis of tubulin, energy substrates
Figure 321. The 4 phases of the cell cycle. In G1 the cell either continues the cycle or enters a quiescent phase called G0. From this phase, most cells can return to the cycle, but some stay in G0 for a long time or even for their entire lifetime. The checking or restriction point (R) in G1 stops the cycle under conditions unfavorable to the cell. When the cell passes this restriction point, it continues the cycle through the synthetic phase (S) and the G2 phase, originating 2 daughter cells in mitosis (M) except when interrupted by another restriction point (not shown) in G2.
Figure 320. Phases of the cell cycle in bone tissue. The G1 phase (presynthesis) varies in duration, which depends on many factors, including the rate of cell division in the tissue. In bone tissue, G1 lasts 25 h. The S phase (DNA synthesis) lasts about 8 h. The G2-plus-mitosis phase lasts 2.53 h. (The times indicated are courtesy of RW Young.)