Apoptosis in Immunology PDF – Current Topics in Microbiology and Immunology



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Preface

In any movement of their life, immune cells, especially T and B lymphocytes, are confronted with an essential choice: to continue their existence or to commit a sort of metabolic suicide that is referred to as apoptosis or programmed cell death. In contrast to most philosophers, lymphocytes and their precursors are constantly susceptible to suicide, and it even appears that the usual cause of T or B cell elimination is suicide rather than death from natural causes, accidents or murder. This book provides a vast overview of lymphocytes suicide: external triggers and internal motives leading to suicidal impulses, accomplices in self-destruction, weapons implicated in self-execution, removal of dead bodies and pharmacological prevention of suicide.
Most of the chapters in this book are devoted to the physiology of apoptosis. The goal is to unmask the external triggers of apoptosis, unravel the signal transduction processes involved therein and describe the role of oncogenes, “death genes” and effector molecules in the apoptotic cascade. The remaining chapters deal with the pathophysiological aspects of lymphocyte apoptosis, namely, as a host contribution to HIV-induced lymphopenia, and therapeutic strategies for the avoidance of lymphocyte death.
We are confident that this compendium will contribute to the exploration of cellular suicide, not only from a basic scientist’s viewpoint but also with regard to the possible clinical implications of apoptosis (dys)regulation. Far from having a depressing effect on the reader, cellular suicide may thus provide a source of both intellectual excitement and therapeutic inspiration.


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Antigen Presentation PDF – Current Topics in Microbiology and Immunology



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Preface

Antigen presentation is a subject most often considered at the molecular level, but its results are, of course, also relevant to the whole organism. This compilation of chapters from experts is aimed at reviewing the broad spectrum from molecular, biochemical and pharmacological considerations through to the effects on host immunity and the diseases which result from defects in these pathways. We begin with the class I MHC pathway. Drs. Nandi, Marusina and Monaco review how the endogenous peptides are generated within the cell and how they are transported into the endoplasmic reticulum. There, the story is taken up by Drs. Fourie and Yang, who relate how the complexes are assembled and transported to the cell membrane. Drs. Hudrisier and Gairin then describe the structure ofthe mature class I complex and reflect upon the pharmacology and possible therapeutic use of peptide antagonists. The following two chapters illustrate the consequences of low class I MHC expression. The defects in immune responsiveness which result from globally defective class I presentation are reviewed by Drs. Frelinger and Serody, who describe the resultant defects in the ability to control challenge by different microbial pathogens, while Dr. RaIl argues that the restricted class I expression, seen in certain tissues of normal animals, is most probably beneficial to the host, preventing immunopathologically mediated cell death. Then, the interface between the host and several viral pathogens is addressed in Chaps. 7 and 8; Drs. Sparer and Gooding describe how adenoviruses interfere with antigen presentation and, thus, with the host’s ability to respond appropriately to the virus challenge. Drs. Johnson and Hill show how, even in a single virus family (the herpes viruses), many different approaches to immune evasion have been taken. In Chap. 9, Drs. Nordeng, Gorvel and Bakke provide an excellent review of the MHC class II pathway, demonstrating that the invariant chain has many and varied functions. In the final chapter, Drs. Eibl and Wolff discuss the consequences of a defective MHC class II pathway in transgenic mouse models and in humans.


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ADP-Ribosylating Toxins PDF – Current Topics in Microbiology and Immunology



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Preface

ADP-ribosylating toxins have been the focus of intensive research for more than 30 years. Researchers from diverse fields of science have taken an interest in these bacterial toxins; they are studied, for example, by microbiologists, biochemists, cell biologists, and pharmacologists. There are two principal reasons for the broad and still growing interest in ADPribosylating toxins. First, insights into the structure and functions of the toxins might be the key to prevention and treatment of diseases caused by the toxin-producing infectious microorganisms. Second, the ADP-ribosylating toxins provide potent and often unique pharmacological tools for the study of the physiological functions of their target proteins. The latter is especially the case with cholera and pertussis toxins, which both modify the IX-subunits of heterotrimeric G-proteins involved in signal transduction pathways. These toxins have proved invaluable in extending our basic understanding of the regulation of hormone-controlled signal transduction.
This volume provides a review and an update of recent studies on the basic properties of bacterial ADP-ribosylating tbxins and/or exoenzymes. Our current knowledge of the cellular entry mechanisms of ADP-ribosylating toxins is reviewed by MADSHUS and STENMARK. WILSON and COLLIER then deal with recent insights into the enzyme mechanism and active site structure of diphtheria toxin and Pseudomonas aeruginosa exotoxin A, which modify elongation factor 2. Toxins which ADP-ribosylate heterotrimeric G-proteins involved in transmembrane signal transduction are the subject of the next two chapters. SERVEN11, Moss and VAUGHAN describe the regulation of adenylate cyclase by cholera toxin and the enhancement of the cholera toxin-induced ADP-ribosylation by guanine nucleotide-binding proteins, the so-called ADP-ribosylation factors, and the review of pertussis toxin by GIERSCHIK lays emphasis on toxin structure-function relationship, toxin-Gprotein interactions and the functional consequences.of G-protein ADP-ribosylation. A chapter by AKTORIES, WILLE, and JUST discusses recently described actin-ADP-ribosylating toxins such as Clostridium botulinum C2 toxin, C. perfringens iota toxin, and other iota-like toxins. Together with the mycotoxins cytochalasin and phalloidin, these ADP-ribosylating toxins appear to be important new tools with which to study the role of actin in various physiological processes. AKTORIES, MOHR, and KOCH deal with clostridial exoenzymes which modify small GTP-binding proteins. C. botulinum C3 ADP-ribosyltransferase, C. limosum exoenzyme, and their eukaryotic protein substrates Rho and Rac are discussed in detail. Last but not least, COBURN briefly reviews P. aeruginosa exoenzyme S. Much less is known about this ADP-ribosyltransferase and its eukaryotic substrates. Recent studies indicate that, again, small GTP-binding proteins (Ras proteins) are the preferred substrates of the enzyme.
This book offers an exciting and comprehensive account of recent developments in the field of ADP-ribosylating toxins and should inspire both further research in this area and the use of these toxins as tools in biological science.


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