Presentation on theme: "From where do cells originate? Why? How?"— Presentation transcript:
1From where do cells originate? Why? How? In This Lesson:Mitosis and the Cell CycleFrom where do cells originate?Why? How?
2Today’s Agenda Chromosome basics. The Cell Cycle. Mitosis. Where division = multiplication.
3By the end of this lesson… You should be able to describe a normally-functioning somatic cell cycle and analyze what would happen if it no longer functioned properly.You should be able to identify several chromosomal diseases using karyotypes.You should be able to contrast mitosis and binary fission.
4The Cell Theory Think back to the cell theory… All living things are made of cells.Cells are the basic units of structure and function.All cells come from preexisting cells.That last one is the big one for us right now.
5You again.You started as a microscopic single cell – a zygote, the cell that resulted from the fusion of gametes – far smaller than the period at the end of this sentence.
6Since then…From that point forward, you’ve been dividing and dividing your cells.Remember, that’s all you are. Just a bunch of overgrown zygotes.Now you’re a trillion-celled living, breathing, thinking emoting human being with a cell phone addiction.
7Why Divide? Growth is just one reason. Cells also divide for Reproduction if they’re unicellular (asexual) or sexual reproduction (gametes – egg or sperm).
8If they’re part of a multicellular organism, they may divide for: Repair or renewal, such as when a cut heals or new skin cells to replace shedding ones.Differentiation, since they need to grow up and get jobs.Not to mention, cells also have to divide because they really can’t get bigger without ruining that whole surface area-to-volume ratio.
11Why do we age? Eventually cells stop being replaced “Apoptosis” Cell death“We die because ourcells die.”William R. Clark
12So what do we need to know? To fully understand the cellular division process, which itself is mostly review of what you’ve already learned, we need to understand the following:ChromosomesThe Cell Cycle
13From females to…bacteria? For most of the rest of this PowerPoint we’re going to be discussing eukaryotic somatic cell division (mitosis), but we do need to get something out of the way first:Binary fission.Binary fission is prokaryotic cell division and it’s pretty simple:Copy DNA.They only have a single, circular, folded-up DNA molecule.Divide.
15Back to Chromosomes [Review] Chromosomes are only visible during mitosis.During other parts of the cell cycle, they’re invisible to a light microscope in a form known as chromatin.Chromatin is simply DNA wrapped around spherical proteins known as histones.The histone/DNA complex is known as a nucleosome.https://www.broadinstitute.org/files/news/images/2010/chromatin_states_2a.png
16“C” Terms Chromosomes Chromatid Long threads of genetic material Found in nucleusChromatidOne side of aduplicated chromosome
17“C” Terms Centromere NOTE Structures that hold sister chromatids togetherNOTE2 sister chromatids = 1 duplicated chromosome
18“C” Terms Chromatin DNA tnagled around a histone (a protein) Condensed chromatin = chromosome
19Terminology [Review] Chromatid Sister Chromatids Centromere Half of a duplicated (X-shaped) chromosome.Sister ChromatidsThe two identical chromatid copies that make up an X-shaped chromosome.CentromereThe site at which the two sister chromatids join.
24And speaking of the cell cycle… The Cell Cycle consists of these stages:G1Gap 1 (growth phase).SSynthesis (DNA is copied).G2Gap 2 (growth phase).New organelles are made.MMitosis (nucleus divides).CytokinesisCytoplasm divides.
25The Cell Cycle [Review] There’s also a bonus stage called G0.That’s pronounced “G naught.”Cells in G0 do not divide by mitosis, like brain cells and some muscle cells.G0 is thus not part of the cell cycle.
26The Cell Cycle [Review] G1, S, and G2 together make up interphase, the collective name for the “resting phase.”“Resting phase” is a bad name.The nucleus is present and easy to spot.DNA is in the form of chromatin.
27The Cell Cycle [Review] During S phase, all six feet of DNA needs to be copied.Error rate in copying? 1 in 100 million DNA bases.With ~30 billion bases in the mammalian genome, that’s around 30 errors each cycle.
28S Phase Chromosomes are copied Terminology [Review]S Phase Chromosomes are copiedSister ChromatidSister ChromatidChromosomeChromosomePre-S PhasePost-S Phase
29Cell Cycle ControlAs you saw in the game, throughout the cell cycle are several checkpoints.During G1 to ensure that S phase can begin.This is the most important signal.If the cell doesn’t get a “go,” it enters G0.After G2 to check that S phase went smoothly and division can occur safely.During M phase (spindle checkpoint) to be certain that spindles have attached to chromosomes correctly.
31Cell Cycle SignalsOkay, I’ve been mentioning “signals” a lot without being specific. Here’s the cast of characters.Internal SignalsCyclins – regulatory proteinsCdks – cyclin-dependent kinases that phosphorylate (activate) cellular proteins.MPF – a mitosis promoting factor.External SignalsDensity-dependent inhibition – cells are inhibited from growing if there are a ton of cells around them.Anchorage dependence – cells need to grow on a substrate.
32Cell Division Frequency First of all, how long does it take the average cell to divide?Embryonic cells = <20 minutesSkin cells = hoursLiver cells = 1-2 years (tend not to divide)Liver cells stay in G0 but can return to the cell cycle if signaled.Nerve and muscle cells = never (after maturity)
33Time for Mitosis. Key organelles in mitosis: Nucleus Centrioles Aid in cell division, remember?Something new: Centrioles are found in a region of the cell known as the centrosome.There is one centrosome for each of the two pairs of centrioles.
36Mitosis [Review] Mitosis (M phase) is the division of the nucleus. There are four main phases of mitosis:ProphaseSome people put an additional step here: Prometaphase.MetaphaseAnaphaseTelophase
37Prophase [Review] Chromatin condenses into chromosomes. Prophase [Review]Chromatin condenses into chromosomes.Chromosomes have been copied by now and look like little X’s.Nuclear membrane/nucleolus breaks down.Mitotic spindle fibers (the “ropes”) forms.The spindle fibers are made of microtubules (actin/myosin).
38PrometaphasePrometaphase is an intermediate step between Prophase and Metaphase (obvious).Starts when the nucleus breaks down and spindle fibers are forming and hooking onto the chromosomes.This centromere/spindle structure is called a kinetochore.Ends when the chromosomes are being moved into the center of the cell.
39http://student. ccbcmd Metaphase [Review]Chromosomes line up in the middle of the cell at the metaphase plate.Sometimes called the equator.
40Anaphase [Review] Centromeres divide. Anaphase [Review]Centromeres divide.Sister chromatids are pulled apart.Chromatids move toward the poles.
41Telophase [Review] Nuclear envelope re-forms. Telophase [Review]Nuclear envelope re-forms.For just a little while, there are two nuclei.These are the daughter nuclei.Chromosomes expand into chromatin.Cytokinesis begins.
42Cytokinesis in Animal Cells [Review] Cytokinesis in Animal Cells [Review]The cell divides into two daughter cells.A belt of actin microfilaments pinches the membrane together between nuclei – forms a cleavage furrow.Cell walls are a little different (next slide).
43Cytokinesis in Plant Cells [Review] Cytokinesis in Plant Cells [Review]Cell plate forms from vesicles, which themselves form a pair of cell membranes (sent from Golgi).Cell wall is inside the vesicle membrane.Cell wall forms on top of the cell plate, dividing the cell into two daughter cells.
49Mitosis SummaryThis really cool company called Hybrid Medical Animations put together an awesome CGI look at mitosis in a cell.
50Summary of MitosisStart with one diploid cell that has 46 chromosomes.46Mitosis4646End with two cells called?They each have how many chromosomes?Two diploid daughter cells each with 46 chromosomes
51Mitosis Fun Facts 300,000,000 cells die and are replaced every minute 50,000,000 cells are born in the time it takes me to read this.Nerve cells do not divide but are replaced from glial cells through neurogenesis.
52Aside: How Old Are You?While it’s true that cells divide relatively quickly, they also don’t last forever.Right now, the oldest cells in your body are 7-9 years old.That’ll stay the same throughout your life – always 7-9 years old, max, for your cells……which means that nothing living about you is actually as old as…you.
56Back to the Cell CycleYou’ve now reviewed all of the cell cycle, from interphase through mitosis and cytokinesis.That’s the “what,” as in, “what is the cell cycle?”We now need to talk about the regulation of the cell cycle.This is the “how,” as in, “how does the cell manage this whole process and keep it from getting out of control?
57Cell Cycle RegulationNormal growth and maintenance of a multicellular creature thus requires careful coordination of cell division.
58Cyclins and Cdk A cyclin is a protein molecule. That’s it. It can’t do anything on its own.There are cyclins for just about every stage in the cell cycle. For example:G1-phase cyclinG1/S-phase cyclinS-phase cyclinM-phase cyclinKey: Their concentration varies throughout the cell cycle.
59Cyclins and Cdk A Cdk is a cyclin-dependent kinase. It’s a kinase, so it phosphorylates stuff to activate it.As you might guess, it needs cyclin to work.Key: Cdk concentration is stable throughout the cell cycle.Cdks bind to cyclins as they are produced.Key: Once Cdk activity passes a certain threshold, the entire cell is driven into the next phase of the cell cycle.
60Cyclins and CdkHey…wait a second. Does something about cyclins and Cdk sound vaguely familiar?Like…maybe…this?
61From Cyclin to Cdk to…Since Cdks, which are themselves just enzymes, play a VERY important role once complexed to a cyclin, the Cdk/cyclin complex is known as an MPF (for mitosis promoting factor).
62MPFs and APCIn addition to the general MPF (mitosis promoting factor), there is also an APC – anaphase promoting complex.Anaphase promoting complex surges in concentration during metaphase…promoting anaphase as the next step.By now you’re probably getting the idea that there are lots of signals in play. In general:The main control mechanism is phosphorylation as carried out by kinases.Internal signals are promoting factors.External signals are growth factors.
63External Signals (Growth Factors) External signals, are released by cells and have effects on others. What kind of effects?Density-dependent inhibition is when crowded cells don’t divide anymore. Why?Growth factors released by cells are bound by so many other cells that no one can get enough growth factor to divide.
64External Signals (Growth Factors) It’s like this:Suppose we are feeding two people with a pizza. Fine. Each person will probably get enough to be full.AKA each cell gets enough growth factor to divide.Now suppose we’re feeding two thousand people with a pizza. People simply aren’t going to get enough to be full.AKA each cell doesn’t get enough growth factor to divide.
65Anchorage DependenceCells have touch receptors that need to be on a proper substrate to grow.Substrate as in “growing surface,” This is called anchorage dependence.Cue the video: NOVA – Artificial Organ Growth
66Case in Point: Growth Factor Let’s take an in-depth look at a growth factor and related processes.This is a fantastic review of a lot of stuff we’ve learned so far.Anything important that we’ve reviewed will be underlined.Anything new and important will be bold and underlined.The growth factor?Platelet-Derived Growth Factor (PDGF)
67Case in Point: Growth Factor The story starts with erythropoietin (EPO), which is a glycoprotein hormone made by the kidney.When renal (kidney) oxygen levels drop too low, kidneys release EPO which stimulates bone marrow to make more red blood cells.Thus the blood can now carry more oxygen, thus enabling greater ATP production through aerobic respiration.This is a negative feedback loop.
68Case in Point: Growth Factor In that way, EPO is a GF of red blood cells.Ever hear about EPO in the news?Coughlancearmstrongcough…Coughblooddopingcough…Armstrong_%28Tour_Down_Under_2009%29.jpg and Lance_Armstrong_MidiLibre_2002.jpg/800px-Lance_Armstrong_MidiLibre_2002.jpg
69Case in Point: Growth Factor EPO has been used as a performance-enhancing drug (PED) (in this case known as “blood doping”) because it increases the oxygen-carrying capacity of the blood by making it extra rich with blood cells.The downside?All those extra blood cells makes your blood considerably thicker/more viscous.Dehydration also makes your blood thicker/more viscous.Thick/viscous blood = increased risk of stroke/heart attack/death.Just say no to EPO.
70Case in Point: Growth Factor But there’s another growth factor involved here.“Another GF? Scandalous!”Forget EPO for a second.Suppose you get a paper cut.
71Case in Point: Growth Factor Platelets in the blood near your cut bind to the neighboring skin cells.They release PDGF (platelet-derived growth factor, remember?).PDGF stimulates neighboring skin cells to divide, healing your wound.Also, platelets stimulate more platelets to arrive and release more PDGF, making this an example of a positive feedback loop.
72So the logical question… We have all these checkpoints.What happens if something goes wrong.In a word?Cancer.Many cancers are caused by cells that escape from the normal cell cycle.The brakes on cell division have been removed.Normal cells divide up to 60 times or so (more on this in a little bit).Cancer cells? A lot more.TED: George Zaidan – How Cancer Cells Behave Differently from Healthy Ones
73Case in Point: HeLa Cells Many cancer cells used in research are called HeLa cells.Named for Henrietta Lacks, a poor African-American woman from the South.In 1951, Lacks sought treatment for cervical cancer. Her doctor(s) took a tissue sample from a tumor and cultured it.“Cultured” meaning “grew in a lab.”Lacks died later in the year, with her family not knowing that her cells had been cultured.Today, her cells are still living and dividing endlessly and are used in research all over the world.Read that book!
74Cancer Terminology Tumor Carcinogen A mass of cancer cells. Remember, cancer cells divide A LOT.Benign tumors are sitting in their original spot.Metastatic or malignant tumors are spreading throughout the body.CarcinogenSomething that causes cancer.Like smoking, chewing tobacco, or other things CB students do in bathrooms.
75Cancerous Growth Factors Proto-oncogenes are genes that cause cancer if switched “on” and mutated.Ras is a group of genes like this and are involved in 30% of human cancers.Tumor-suppressor genes cause cancer if switched “off.”p53 is a tumor-suppressor gene and is involved in 50% of human cancers.So it follows that mutagens are things that cause mutations and may also be carcinogens.
76Cancerous Growth Factors Another factor in play is the degradation of telomeres.Telomeres are “caps” on the ends of the chromosomes that are made of junk DNA.With each cell division, however, telomeres get smaller.
77Aside: The Hayflick Limit In the 1960s, Leonard Hayflick discovered that there was a limit to how many times cells could divide before their telomeres were eroded completely away.That number is somewhere between 52 and 60 times, and it’s now called the Hayflick Limit.After that point, the cells may either be told to die (apoptosis – programmed cell death) or simply won’t divide anymore.
79How does cancer work?Cancerous genes or cells are often found to be activating lots of cyclins, thus pushing the cell through the cell cycle too rapidly.Tumor suppressor genes prevent errant DNA from being copied in mitosis.p53, for example, stops cell division if bad DNA is found, but if p53 isn’t working…you get the idea.Subsequent growth and spread of tumors can begin to block blood vessels, clog body systems, prevent other cells from functioning…the list goes on…
80Case in Point: p53 Step 1 Step 2 Step 3 Step 1 Step 2 Step 3 NORMAL p53p53 allows cellswith repairedDNA to divide.p53proteinDNA repair enzymep53proteinStep 1Step 2Step 3DNA damage is causedby heat, radiation, orchemicals.Cell division stops, and p53 triggers enzymes to repair damaged region.p53 triggers the destruction of cells damaged beyond repair.ABNORMAL p53abnormalp53 proteincancercellStep 1Step 2DNA damage iscaused by heat,radiation, orchemicals.The p53 protein fails to stopcell division and repair DNA.Cell divides without repair todamaged DNA.Step 3Damaged cells continue to divide.If other damage accumulates, thecell can turn cancerous.
81Cancer MutationsThere are six key mutations that must happen for cancer to occur:Unlimited growthGrowth promoter genes turned on.Ignore checkpointsTumor suppressor genes turned off.Escape apoptosisSuicide genes turned off.ImmortalityChromosome maintenance genes turned on.Blood vessel growthBlood vessel growth genes turned on.Anchorage/density-independenceTouch sensor genes turned off.
82Cancer Treatments High-Energy Radiation Chemotherapy Gleevec Kill rapidly-dividing cells.ChemotherapyStop DNA replication, mitosis/cytokinesis, and blood vessel growth.GleevecA relatively new anti-cancer drug that targets enzymes found only in cancer cells.