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Chapter 3 Cells Copyright  The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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Presentation on theme: "Chapter 3 Cells Copyright  The McGraw-Hill Companies, Inc. Permission required for reproduction or display."— Presentation transcript:

1 Chapter 3 Cells Copyright  The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

2 The Cell Cycle Series of changes a cell undergoes from the time it forms until the time it divide Stages: Interphase Mitosis Cytokinesis The cell cycle is highly regulated. Most cells do not divide continually. Cells have a maximum number of times they can divide because of built-in “clocks” (telomeres) on the tips of chromosomes. G2 phase Interphase Prophase Mitosis S phase: genetic material replicates Metaphase Anaphase Telophase G1 phase cell growth Cytokinesis Proceed to division Remain specialized Restriction checkpoint Apoptosis

3 Interphase Very active period Cell grows
Cell maintains routine functions Cell replicates genetic material to prepare for nuclear division Cell synthesizes new organelles to prepare for cytoplasmic division Phases: G phases – cell grows and synthesizes structures other than DNA S phase – cell replicates DNA

4 Mitotic Cell Division Produces two daughter cells from an original somatic cell Nucleus divides – mitosis Cytoplasm divides – cytokinesis Phases of mitosis (the process is actually continuous): Prophase – the first stage of mitosis, results in the DNA condensing into chromosomes, centrioles migrating to the poles, microtubules of the cytoskeleton reorganizing into spindle fibers, and the disappearance of the nuclear membrane.

5 Mitotic Cell Division Metaphase – occurs as spindle fibers attach to centromeres on the chromosomes and the chromosomes align midway between centrioles. Anaphase – occurs as the spindle fibers contract and pull the sister chromatids toward the centrioles. Telophase – the final stage of mitosis, begins when the chromosomes have completed their migrations, the nuclear envelope reappears, and the chromosomes begin to unwind.

6 Mitosis Late Interphase Cell has passed the restriction checkpoint
and completed DNA replication, as well as replication of centrioles and mitochondria, and synthesis of extra membrane. Early Interphase of daughter cells— a time of normal cell growth and function. (a) Restriction checkpoint Nuclear envelope Chromatin fibers Centrioles Cleavage furrow Aster Prophase Chromosomes condense and become visible. Nuclear envelope and nucleolus disperse. Spindle apparatus forms. Microtubules (e) (b) Centromere Spindle fiber Late prophase Chromosomes Sister chromatids Nuclear envelopes Telophase and Cytokinesis Nuclear envelopes begin to reassemble around two daughter nuclei. Chromosomes decondense. Spindle disappears. Division of the cytoplasm into two cells. (d) (c) Mitosis Cytokinesis G1 phase Anaphase Sister chromatids separate to opposite poles of cell. Events begin which lead to cytokinesis. Metaphase Chromosomes align along equator, or metaphase plate of cell. S phase Interphase G2 phase © Ed Reschke

7 Cytoplasmic Division Also known as cytokinesis Begins during anaphase
Continues through telophase Contractile ring pinches cytoplasm in half The two daughter cells may have varying amounts of cytoplasm and organelles, but they share identical genetic information.

8 Cell Differentiation 1. The process by which cells develop into different types of cells with specialized functions is called differentiation. 2. Cell differentiation reflects genetic control of the nucleus as certain genes are turned on while others are turned off.

9 Animation: Mitosis and Cytokinesis
Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at

10 Animation: Control of the Cell Cycle
Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at

11 Control of Cell Division
Cell division capacities vary greatly among cell types Skin and blood cells divide often and continually Neuron cells divide a specific number of times then cease Chromosome tips (telomeres) that shorten with each mitosis provide a mitotic clock Cells divide to provide a more favorable surface area to volume relationship Growth factors and hormones stimulate cell division Hormones stimulate mitosis of smooth muscle cells in uterus Epidermal growth factor stimulates growth of new skin Contact (density dependent) inhibition Tumors are the consequence of a loss of cell cycle control

12 Tumors Two types of tumors: Benign – usually remains localized
Malignant – invasive and can metastasize; cancerous Normal cells (with hairlike cilia) Two major types of genes cause cancer: Oncogenes – activate other genes that increase cell division Tumor suppressor genes – normally regulate mitosis; if inactivated they are unable to regulate mitosis Cells are now known as “immortal” Cancer cells

13 Animation: How Tumor Suppressor Genes Block Cell Division
Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at

14 Stem and Progenitor Cells
Differentiation: specialization of cells Stem cell: Can divide to form two new stem cells Self-renewal Can divide to form a stem cell and a progenitor cell Totipotent – can give rise to every cell type Pluripotent – can give rise to a restricted number of cell types Progenitor cell: Committed cell Can divide to become any of a restricted number of cells Pluripotent

15 Stem and Progenitor Cells
Sperm Egg Sebaceous gland cell Progenitor cell Fertilized egg Progenitor cell Skin cell Stem cell Progenitor cell Progenitor cell Stem cell Neuron Progenitor cell Progenitor cell Progenitor cell Astrocyte Progenitor cell Progenitor cell Progenitor cell Bone cells one or more steps Fibroblasts (a connective tissue cells) produces another stem cell (self-renewal) Blood cells and platelets

16 Cell Death Apoptosis: Programmed cell death
Acts as a protective mechanism Is a continuous process Normal part of development Death receptor on doomed cell binds signal molecule. Caspases are activated within. Caspases destroy various proteins and other cell components. Cell becomes deformed. Blebs Cell fragments Phagocyte attacks and engulfs cell remnants. Cell components are degraded.


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