Chapter 6 a Tour of the Cell
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
A Tour of the Cell Overview
Unit 3: The Cell Name______________________ Chapter 6: A Tour of the Cell Overview 6.1 Biologists use microscopes and the tools of biochemistry to study cells The discovery and early study of cells progressed with the invention of microscopes in 1590 and their improvement in the 17th century. In a light microscope (LM), visible light passes through the specimen and then through glass lenses. ○ The lenses refract light so that the image is magnified into the eye or a camera. Microscopes vary in magnification, resolution, and contrast. ○ Magnification is the ratio of an object’s image to its real size. A light microscope can magnify effectively to about 1,000 times the real size of a specimen. ○ Resolution is a measure of image clarity. It is the minimum distance two points can be separated and still be distinguished as two separate points. The minimum resolution of an LM is about 200 nanometers (nm), the size of a small bacterium. ○ Contrast accentuates differences in parts of the sample. It can be improved by staining or labeling of cell components so they stand out. Although an LM can resolve individual cells, it cannot resolve much of the internal anatomy, especially the organelles, membrane-enclosed structures within eukaryotic cells. The size range of cells 1 To resolve smaller structures, scientists use an electron microscope (EM), which focuses a beam of electrons through the specimen or onto its surface. ○ Theoretically, the resolution of a modern EM could reach 0.002 nm, but the practical limit is closer to about 2 nm. Scanning electron microscopes (SEMs) are useful for studying the surface structure or topography of a specimen. -
The Endomembrane System and Proteins
Chapter 4 | Cell Structure 121 Endosymbiosis We have mentioned that both mitochondria and chloroplasts contain DNA and ribosomes. Have you wondered why? Strong evidence points to endosymbiosis as the explanation. Symbiosis is a relationship in which organisms from two separate species depend on each other for their survival. Endosymbiosis (endo- = “within”) is a mutually beneficial relationship in which one organism lives inside the other. Endosymbiotic relationships abound in nature. We have already mentioned that microbes that produce vitamin K live inside the human gut. This relationship is beneficial for us because we are unable to synthesize vitamin K. It is also beneficial for the microbes because they are protected from other organisms and from drying out, and they receive abundant food from the environment of the large intestine. Scientists have long noticed that bacteria, mitochondria, and chloroplasts are similar in size. We also know that bacteria have DNA and ribosomes, just like mitochondria and chloroplasts. Scientists believe that host cells and bacteria formed an endosymbiotic relationship when the host cells ingested both aerobic and autotrophic bacteria (cyanobacteria) but did not destroy them. Through many millions of years of evolution, these ingested bacteria became more specialized in their functions, with the aerobic bacteria becoming mitochondria and the autotrophic bacteria becoming chloroplasts. The Central Vacuole Previously, we mentioned vacuoles as essential components of plant cells. If you look at Figure 4.8b, you will see that plant cells each have a large central vacuole that occupies most of the cell's area. The central vacuole plays a key role in regulating the cell’s concentration of water in changing environmental conditions. -
Vesicle Traffic in the Endomembrane System: a Tale of Cops, Rabs and Snares Andreas Nebenführ
507 Vesicle traffic in the endomembrane system: a tale of COPs, Rabs and SNAREs Andreas Nebenführ Recent years have seen remarkable progress in our contrast, mammalian cells have an intermediate recycling understanding of the endomembrane system of plants. A large compartment between the ER and the Golgi, the vesiculo- number of genes and proteins that are involved in membrane tubular cluster (VTC), that does not exist in plants. exchange between the different compartments of this system have been identified on the basis of their similarity to animal The transport of proteins and membranes between the and yeast homologs. These proteins indicate that the different compartments of the endomembrane system is endomembrane system in plants functions in essentially the mediated by small carriers, the transport vesicles. The same way as those in other eukaryotes. However, a growing basic mechanisms involved in membrane-exchange reactions number of examples demonstrate that the dynamic interplay appear to be the same, irrespective of the organelles between membrane-exchange proteins can be regulated involved [2]. The initial step involves the formation of a differently in plant cells. Novel tools and a better understanding proteinaceous membrane coat that plays a two-fold role. of the molecular effects of the inhibitor brefeldin A are helping First, coat proteins deform the membrane so as to form a to unravel these plant-specific adaptations. bud and eventually a vesicle, and second, they are involved in cargo selection. The assembly of the coat is Addresses controlled by a small GTPase of the Ras superfamily, University of Tennessee, Department of Botany and School of which in turn is activated by a specific guanidine-nucleotide Genome Science and Technology, 437 Hesler Biology, Knoxville, exchange factor (GEF). -
Endomembrane System
Cell Structure & Function Cell Theory Cells are fundamental to biology Cells are the basic living units within organisms (all chemical rxns. of life take place within cells) All organisms are made of cells Single-celled organisms (bacteria/protists) Multicellular organisms (plants/animals/fungi) Cell Structure & Function Basic Aspects of Cell Structure & Function Plasma membrane Lipid bilayer Proteins DNA-containing region Cytoplasm Eukaryotic v. Prokaryotic cells Prokaryotic v. Eukaryotic Cells Two major classes of cells Prokaryotic cells (pro-, “before”) Cell lacks a “true” nucleus DNA is coiled in a nucleoid region Cells lack nuclear membrane Prokaryotic v. Eukaryotic Cells [attachment structure] [DNA location] [organelles that synthesize proteins] [enclosing the cytoplasm] [rigid structure outside the p.m. ] [jelly-like outer coating] [locomotion organelle] Prokaryotic v. Eukaryotic Cells Eukaryotic cells (eu-, “true”) Nucleus contains most of the cells nuclear material, DNA usually the largest organelle Bordered by a membranous envelope Prokaryotic v. Eukaryotic Cells Plant v. Animal Cells Both contain Plasma membrane (functions as a selective barrier) Nucleus (gene-containing organelle) Cytoplasm (region between nucleus and p.m.) Consists of organelles in a fluid (cytosol) Prokaryotic v. Eukaryotic Cells Plant v. Animal Cells Organelles Bordered by internal membranes Compartmentalizes the functions of a cell Maintains organelle’s unique environment Most organelles are found in both plant and animal cells Plant v. Animal Cells -
Cell and Cell Division
Cell and Cell Division Chapter 2 Lecture Outline Cell Cell membrane Nucleus: Nuclear Envelope, Nucleoplasm and Chromatin (DNA + Histones) Cytoplasm: Cytosol and Cell Organelles Cell Division Cell Cycle Mitosis: division of nucleus Cytokinesis: division of cytoplasm Cell Theory 4 basic concepts of cell theory are: Cells are the units of structure (building blocks) of all organisms Cells are the smallest unit of function in all organisms Cells originate only from pre-existing cells by cell division. All cells maintain homeostasis (internal conditions within limits) Cell Membrane All cells are covered with a thin covering of a double layer of Phospholipids and associated Proteins present here and there. Each phospholipid has a polar (hydrophilic) head and non-polar (hydrophobic) tails. In the double layer the tails face each other forming a hydrophobic barrier which keeps water dissolved contents inside. Proteins may be Intrinsic – embedded in the lipid double layer and Extrinsic associated outside the lipid double layer. Cytoplasm Cytoplasm is the living fluid part between cell membrane and nucleus. It has special structures called Cell Organelles in it. Cytosol is the liquid part of cytoplasm formed of water having dissolved or suspended substances in it. Cell Organelles are organ like each performing specific function/s but formed of molecules and membranes only (sub-cellular). Double Membrane bound Organelles: Mitochondria, Chloroplasts, Endoplasmic Reticulum, Golgi Body, and Nucleus. Single Membrane bound Organelles: Lysosomes, Peroxisomes, Vacuoles Organelles lacking any membrane: Ribosomes, Centrioles, Nucleolus Nucleus and Ribosomes 1 Genetic Control of the Cell Nucleus: is the most distinct structure inside cell visible with light microscope. -
Endomembrane System– Endoplasmic Reticulum, Golgi Apparatus, Lysosomes, Peroxisomes, Vacuoles, Vesicles
Chapter 7. The Cell: Endomembrane System– Endoplasmic Reticulum, Golgi Apparatus, Lysosomes, Peroxisomes, Vacuoles, Vesicles AP Biology 2005-2006 Overview . Play key role in synthesis (& hydrolysis) of macromolecules in cell . Various “players” modify macromolecules for various functions AP Biology 2005-2006 Endoplasmic Reticulum . Function manufactures membranes & performs many bio-synthesis functions . Structure membrane connected to nuclear envelope & extends throughout cell accounts for 50% membranes in eukaryotic cell . rough ER = bound ribosomes . smooth ER = no ribosomes AP Biology 2005-2006 Types of ER AP Biology 2005-2006 Smooth ER function . Factory processing operations many metabolic processes . synthesis & hydrolysis enzymes of smooth ER… . synthesize lipids, oils, phospholipids, steroids & sex hormones . hydrolysis (breakdown) of glycogen (in liver) into glucose . detoxify drugs & poisons (in liver) ex. alcohol & barbiturates AP Biology 2005-2006 Rough ER function . Produce proteins for export out of cell protein secreting cells packaged into transport vesicles for export which cells have a lot of rough ER? AP Biology 2005-2006 Membrane Factory . Synthesize membrane phospholipids build new membrane as ER membrane expands, bud off & transfer to other parts of cell that need membranes . Synthesize membrane proteins membrane bound proteins synthesized directly into membrane processing to make glycoproteins AP Biology 2005-2006 AP Biology 2005-2006 AP Biology 2005-2006 Golgi Apparatus . Function finishes, sorts, & ships cell products . “shipping & receiving department” center of manufacturing, warehousing, sorting & shipping extensive in cells specialized for secretion which cells have a lot AoP Bf iGoloogylgi? 2005-2006 Golgi Apparatus . Structure flattened membranous sacs = cisternae . look like stack of pita bread 2 sides = 2 functions . cis = receives material by fusing with vesicles = “receiving” . -
Cytoplasmic Membrane Systems
Cytoplasmic Membrane Systems Under the light microscope, the cytoplasm of living cells appears relatively devoid of structure. Yet, even before the beginning of the twentieth century, examination of stained sections of animal tissues hinted at the existence of an extensive membrane network within the cytoplasm. It became evident from the early electron microscopic studies and the biochemical investigations that followed that the cytoplasm of eukaryotic cells was subdivided into a variety of distinct compartments bounded by membrane barriers. Just as a house or restaurant is divided into specialized rooms where different activities can take place independent of one another, the cytoplasm of a cell is divided into specialized membranous compartments for analogous reasons. 1 2 The organelles of the endomembrane system are part of a dynamic, integrated network in which materials are shuttled back and forth from one part of the cell to another. For the most part, materials are shuttled between organelles—from the Golgi complex to the plasma membrane, for example—in small, membrane-bounded transport vesicles that bud from a donor membrane compartment. When they reach their destination, the vesicles fuse with the membrane of the acceptor compartment, which receives the vesicle’s soluble cargo as well as its membranous wrapper. Repeated cycles of budding and fusion shuttle a diverse array of materials along numerous pathways that traverse the cell. 3 A biosynthetic pathway can be discerned in which proteins are synthesized in the endoplasmic reticulum, modified during passage through the Golgi complex, and transported from the Golgi complex to various destinations, such as the plasma membrane, a lysosome, or the large vacuole of a plant cell. -
The Neuronal Endomembrane System III
0270.6474/85/0512-3135$02.00/O The Journal of Neuroscience Copyright 0 Society for Neuroscience Vol. 5, No. 12. pp. 3135-3144 Pnnted in U.S.A. December 1985 The Neuronal Endomembrane System III. The Origins of Axoplasmic Reticulum Discrete Axonal Cisternae the Axon Hillock’ JAMES D. LINDSEY2 AND MARK H. ELLISMAN Department of Neurosciences, University of California, San Diego, School of Medicine, La Jolla, California 92093 Abstract The axoplasmic reticulum (AR) and the discrete element vesicles were usually found in close association with the (e.g., vesicles, vesiculotubular bodies, multivesicular bodies, trans face of the Golgi apparatus. These results indirectly etc.) constitute the endomembrane system of the axon. It is support the hypothesis that vectors of fast axonal transport, reported here that the AR of bullfrog sciatic nerve readily fills namely the discrete elements, form directly at the trans face with osmium deposits during osmium impregnation. In con- of the Golgi apparatus. From here they move toward and trast, the discrete elements and mitochondria are highly subsequently down the axon without any membrane fission- resistant to impregnation. Hence this preparation is well fusion events with either RER or AR. AR, although it forms suited to address the nature of possible interactions between continuities with RER, retains a distinctly different chemical AR and rough endoplasmic reticulum (RER) in the axon composition from RER as evidenced by its much higher hillock. It is also ideal to study the origin of the axonal discrete affinity for osmium. Thus, it should be considered as an elements within the cell body as well as their interaction with endomembrane component separate from, although inti- other somal endomembrane system components. -
Growth Cone-Localized Microtubule Organizing Center Establishes
RESEARCH ARTICLE Growth cone-localized microtubule organizing center establishes microtubule orientation in dendrites Xing Liang1,2†, Marcela Kokes1,2†, Richard D Fetter2, Maria Danielle Sallee1, Adrian W Moore3, Jessica L Feldman1*, Kang Shen1,2* 1Department of Biology, Stanford University, Stanford, United States; 2Howard Hughes Medical Institute, Stanford University, Stanford, United States; 3RIKEN Center for Brain Science, Wako, Japan Abstract A polarized arrangement of neuronal microtubule arrays is the foundation of membrane trafficking and subcellular compartmentalization. Conserved among both invertebrates and vertebrates, axons contain exclusively ‘plus-end-out’ microtubules while dendrites contain a high percentage of ‘minus-end-out’ microtubules, the origins of which have been a mystery. Here we show that in Caenorhabditis elegans the dendritic growth cone contains a non-centrosomal microtubule organizing center (MTOC), which generates minus-end-out microtubules along outgrowing dendrites and plus-end-out microtubules in the growth cone. RAB-11-positive endosomes accumulate in this region and co-migrate with the microtubule nucleation complex g- TuRC. The MTOC tracks the extending growth cone by kinesin-1/UNC-116-mediated endosome movements on distal plus-end-out microtubules and dynein clusters this advancing MTOC. Critically, perturbation of the function or localization of the MTOC causes reversed microtubule polarity in dendrites. These findings unveil the endosome-localized dendritic MTOC as a critical organelle for establishing axon-dendrite polarity. *For correspondence: [email protected] (JLF); [email protected] (KS) †These authors contributed Introduction equally to this work The ability of our nervous system to function rests on polarized transport within the axons and den- drites of neurons, a task performed by molecular motors running on a polarized microtubule (MT) Competing interest: See network. -
Cell and Cell Division
Cell and Cell Division Chapter 2 Lecture Outline Cell Cell membrane Nucleus: Nuclear Envelope, Nucleoplasm and Chromatin (DNA + Histones) Cytoplasm: Cytosol and Cell Organelles Cell Division Cell Cycle Mitosis: division of nucleus Cytokinesis: division of cytoplasm Cell Theory 4 basic concepts of cell theory are: Cells are the units of structure (building blocks) of all organisms Cells are the smallest unit of function in all organisms Cells originate only from pre-existing cells by cell division. All cells maintain homeostasis (internal conditions within limits) Cell Membrane All cells are covered with a thin covering of a double layer of Phospholipids and associated Proteins present here and there. Each phospholipid has a polar (hydrophilic) head and non-polar (hydrophobic) tails. In the double layer the tails face each other forming a hydrophobic barrier which keeps water dissolved contents inside. Proteins may be Intrinsic – embedded in the lipid double layer and Extrinsic associated outside the lipid double layer. Cytoplasm Cytoplasm is the living fluid part between cell membrane and nucleus. It has special structures called Cell Organelles in it. Cytosol is the liquid part of cytoplasm formed of water having dissolved or suspended substances in it. Cell Organelles are organ like each performing specific function/s but formed of molecules and membranes only (sub-cellular). Double Membrane bound Organelles: Mitochondria, Chloroplasts, Endoplasmic Reticulum, Golgi Body, and Nucleus. Single Membrane bound Organelles: Lysosomes, Peroxisomes, Vacuoles Organelles lacking any membrane: Ribosomes, Centrioles, Nucleolus Nucleus and Ribosomes 1 Genetic Control of the Cell Nucleus: is the most distinct structure inside cell visible with light microscope. -
The Nuclear Envelope During Mitosis
Available online at www.sciencedirect.com ScienceDirect § Breaking down the wall: the nuclear envelope during mitosis 1 1,2 Christine J Smoyer and Sue L Jaspersen A defining feature of eukaryotic cells is the nucleus, which assemble an intranuclear spindle. As we discuss below, houses the genome inside the nuclear envelope (NE): a double eukaryotic cells utilize both strategies, as well as vari- lipid bilayer that separates the nuclear and cytoplasmic ations in between (Figure 1), offering glimpses into how materials. Although the NE is commonly viewed as a barrier that the nucleus evolved as an organelle to organize and is overcome only by embedded nuclear pore complexes protect the genome and why mutations in NE proteins (NPCs) that facilitate nuclear-cytoplasmic trafficking, recent result in a broad spectrum of human diseases, including work in a wide range of eukaryotes reveals that the NE is a cancer [1,2]. dynamic organelle that is modified each time the cell divides to ultimately establish two functional daughter nuclei. Here, we The nuclear envelope review how studies of divergent mitotic strategies have helped Although multiple theories exist on how the eukaryotic elucidate common properties of NE biology that allow it to nucleus arose during evolution, most share the idea that function throughout the cell cycle. the NE and its associated proteins have ancient roots in Addresses division of the genome [1,3]. The nucleus likely co- 1 Stowers Institute for Medical Research, Kansas City, MO 64110, United evolved with other parts of the endomembrane system. States 2 However, unlike other cellular membranes, the NE is a Department of Molecular and Integrative Physiology, University of double lipid bilayer composed of an outer (ONM) and Kansas Medical Center, Kansas City, KS 66160, United States inner membrane (INM) separated by a perinuclear space. -
The Neuronal Endomembrane System I
0270.6474/65/0512-3111$02.00/0 The Journal of Neuroscience Copyright 0 Soctety for Neuroscience Vol. 5, No. 12, pp. 3111-3123 Prlnted in U.S.A. December 1985 The Neuronal Endomembrane System I. Direct Links between Rough Endoplasmic Reticulum and the cis Element of the Golgi Apparatus’ JAMES D. LINDSEY* AND MARK H. ELLISMAN Department of Neurosciences, University of California, San Diego, School of Medicine, La Jolla, California 92093 Abstract This is the first of three papers describing new components formed confluent bridges between the cis element and RER. and structural relationships within the neuronal endomem- In addition, the varicose tubules were found to bridge widely brane system. This system includes: the nuclear envelope, separated elements of RER. Finally, numerous examples of rough endoplasmic reticulum, the Golgi apparatus, lyso- varicose and smooth tubules were seen to extend from RER somes, axoplasmic reticulum, and discrete cytoplasmic com- and from cis elements to eventually form blind endings. partments such as vesicles, multivesicular bodies, and so These findings raise the possibility that the tubules form on. Previous high voltage electron microscope studies of highly dynamic transitory connections between RER and the osmium-impregnated Golgi apparatus have shown that small Golgi apparatus as well as between separated elements of varicose tubules often arise from the cis element. In bullfrog RER. Those between RER and Golgi apparatus are ideally spinal ganglia, these tubules have been seen to extend into positioned to play a major role in the transfer of protein or cytoplasmic domains occupied by rough endoplasmic retic- lipid components first assembled in RER to the Golgi appa- ulum (RER).