REVIEWS

Book reviewed in this article:
Vegetatio: Acta Geobotanica: International Review of Plant Sociology, Ecology and Plant Geography. Dr W. Junk
Die Pilze. BY ERNST GAUMANN
Hydrobiologia: Acta Hydrobiologica Limnologica et Protistologica. Dr W. Junk
Physiologia Comparata et Oecologia: an International Journal of Comparative Physiology and Ecology. Dr W. Junk
The Avian Egg. By ALEXIS L. ROMANOFF and ANASTASIA J. ROMANOFF     

Besprechungen

Book review in this article
Handbuch der Pflanzenkrankheiten. Begründet von Paul Sorauer. III. Band: Pilzliche Krankheiten und Unkräuter. 6., vollständig neugestaltete Auflage in 6 Lieferungen. Herausgegeben von Prof. Dr. H. Richter. Verlag Paul Parey, Berlin und Hamburg. 4. Lieferung: Basidiomycetes. Bearbeitet von Prof. Dr. K. Hassebrauk, Dr. E. Niemann, Dr. G. Schuhmann, Prof. Dr. H. Zycha.
Dünnschicht-Chromatographie. Ein Laboratoriumshandbuch. Bearbeitet von verschiedenen Fachgelehrten. Herausgegeben von E. STAHL.
Siegel, S. M., The Plant Cell Wall. (Int. Series of Monographs on Pure and Applied Biology, Division: Plant Physiology, Bd. 2).     

The IUPS Physiome Project: a framework for computational physiology

The IUPS Physiome Project is an internationally collaborative open-source project to provide a public domain framework for computational physiology, including the development of modelling standards, computational tools and web-accessible databases of models of structure and function at all spatial scales. A number of papers in this volume deal with the development of specific mathematical models of physiological processes. This paper stands back from the detail of individual models and reviews the current state of the IUPS Physiome Project including organ and organ system continuum models, the interpretation of constitutive law parameters in terms of micro-structural models, and markup languages for standardizing cellular processes. Some current practical applications of the physiome models are given and some of the challenges for the next 5 years of the Physiome Project at the level of organs, cells and proteins are proposed.     

Teaching and learning in the interactive classroom

The Claude Bernard Distinguished Lectureship of the Teaching of Physiology Section is presented annually at the Experimental Biology meeting. The lectureship is named for Prof. Claude Bernard, the experimental physiologist who is credited with introducing the concept of homeostasis. The 2006 Claude Bernard Distinguished Lecture was given by Dr. Dee U. Silverthorn from the University of Texas at Austin, TX.     

Buchbesprechung

Abstract

Herausgegeben von Prof. Dr. Dr. h.c. mult. Manfred Kirchgessner Freising-Weihenstephan

Unter Mitwirkung zahlreicher Wissenschaftler

Heft 22 der “Fortschritte in der Tierphysiologie und Tierernährung”; Beihefte zur “Zeitschrift für Tierphysiologie, Tierernährung und Futtermittelkunde” (“Advances in Animal Physiology and Animal Nutrition”; Supplements to “Journal of Animal Physiology and Animal Nutrition”)

1991. 120 Seiten. Mit 41 Abbildungen und 58 Tabellen.

25 × 17 cm. Kartoniert 62, — DM. ISBN 3-490-42215-5-. Verlag Paul Parey. Hamburg und Berlin Reviewed by A. Püschner. Reviwed by A. Püschner.     

Behavioural responses of the pine weevilHylobius abietis L. (Col.: Curculionidae) to odours activating different groups of receptor cells

Summary A method for measuring the attractive effect of odorous compounds on a population of pine weevilsHylobius abietis L. is described. Three substances, which strongly activated different groups of sensory cells (Mustaparta, 1975) were examined. Trans-verbenol, which excited selectively certain trichodeal cells had the highest attraction and dominated the attractive effect of -pinene. The latter activated a special group of basiconic cells which indicated its importance as food attractant. The third compound, 5-hexen-2-one, activated a large number of olfactory receptor cells, but had almost no attractive effect on the weevils.This work was financed by the Norwegian Research Council for Sciences and Humanities NAVF, and also supported by Deutsche Akademische Austauschdienst DAAD.I would like to thank Dr. S. Gothilf, Israel Institute for Biological Research, Tel Aviv, Dr. J. Jansen, Institute of Physiology, University of Oslo, and Dr. S. Grillner, Institute of Physiology, University of Gothenborg, for discussions. For constantly providing insects I am thankful to Oberforstmeister H. Niemeyer, Niedersächsische Forstliche Versuchsanstalt, Göttingen.     

Distribution of IAA and ABA in gravistimulated primary roots ofZea mays. L.

The transport of¹⁴C-IAA and¹⁴C-ABA applied exogenously to root cap toward the elongation zone was investigated in gravi- and light-stimulated primary roots ofZea mays L. cv. Golden Cross Bantam 70. No significant difference of either IAA or ABA in radioactivities was observed between upper and lower halves of elongation zones during the latent period (0–60 min after the stimulation) of gravitropic response. When quantitative analysis of endogenous IAA and ABA by an internal standard method was carried out 60 min after gravi- and/or light-stimulation, no asymmetric redistribution of either IAA or ABA was observed between upper and lower halves of elongation zones. Light irradiation increased by 20% the contents of ABA in elongation zones. These results suggest that although both IAA and ABA are basipetally transportable and can transmit their information to the elongation zone during a latent period we cannot explain the gravitropic curvature by their redistributions between the two (upper and lower) halves of primary roots ofZea. On the basis of results from the present work and previous papers, the distribution of IAA and ABA in gravistimulatedZea roots is discussed. A part of this study was reported at the Eighth Annual Meeting of the IUPS Commission on Gravitational Physiology at Tokyo 1986.     

Secondary sensory cells in the gravity receptor system of the statocyst of Octopus vulgaris

Summary The presence of secondary sensory cells in the Octopus gravity receptor system has been demonstrated. In serial thin sections of the receptor cells (hair cells) no axons were found leaving the cells. Instead, synapses were observed with synaptic vesicles lying inside the receptor cells. Both data clearly indicate that the receptor hair cells represent secondary sensory cells. In addition, efferent contacts to the receptor cells could be confirmed.This work was supported in part by grant Wo 160/5 of the Deutsche Forschungsgemeinschaft to Prof. Dr. H.G. WolffThe experimental work was done in part at the Zoological Station in Naples and at the Sechenov Institute of Evolutionary Physiology and Biochemistry of the USSR Academy of Sciences (Laboratory of Prof. Dr. Ya.A. Vinnikov), Leningrad, USSR. The authors thank Prof. Vinnikov and Dr. Tsirulis for stimulating discussions     

Selman A. Waksman,Winner of the 1952 Nobel Prize for Physiology or Medicine

The history of the discovery and development of streptomycin is reviewed here from the personal standpoint of a member of Dr. Selman Waksman''s antibiotic screening research team. The team approach of eight individuals illustrates how the gradual enhancement of the screening methodology was developed. I illustrate three study periods with key aspects in the development of streptomycin which led to a Nobel Prize being granted to Professor Waksman. One item not previously emphasized is the employment of a submerged culture technique for large-scale production of streptomycin, thus enabling rapid animal testing and human clinical trials with Mycobacterium tuberculosis. Another is that purified streptomycin was shown by Dr. Waksman to be distinctly different from the substances called natural products, which are no longer patentable in the United States; therefore, streptomycin was found to be patentable. A third item not previously emphasized is his emphasis on the screening of actinomycetes, including the newly named Streptomyces genus. All of these factors contributed to the success of streptomycin in the treatment of tuberculosis. In combination, their successes led to Dr. Waksman''s department becoming a new pharmacological research area, specializing in drug discovery. These unique accomplishments all burnish the prior rationales used by the Karolinska Institute in granting Dr. Waksman alone the 1952 Nobel Prize for Physiology or Medicine.     

REVIEWS

Book reviewed in this article:
Colour-changes in Animals. The Pigmentary Effector System: A Review of the Physiology of Colour Response . By Dr L ancelot H ogben .
Outlines of Fungi and Plant Diseases for Students and Practitioners of Agriculture and Horticulture . By F. T. B ennet .
The Evolution of Plants . By D uckenfield H enry S cott . Home University Library.
An Introduction to the Study of Heredity . By E. W. M acbride .
The Biological Foundations of Society . By A rthur D endy .     

Staphylococcus aureus alpha-toxin-induced pores: Channel-like behavior in lipid bilayers and patch clamped cells

The conductance of pores induced by Staphylococcus aureus -toxin in Lettre cells has been compared to that in bilayers composed of synthetic lipids or Lettre cell membrane constituents. Previously described characteristics of toxin-induced conductance changes in lipid bilayers, namely rectification, voltage-dependent closure, and closure at low pH or in the presence of divalent cations (Menestrina, 1986) are displayed also in bilayers prepared from Lettre cell membranes and in patch clamped Lettre cells. It is concluded that endogenous proteins do not affect the properties of -toxininduced channels significantly and that the relative lack of ion channels in Lettre cells makes them ideal for studies of pore-forming toxins by the patch clamp technique.Dr. Sviderskaya is on leave of absence from the Physiology Institute, University of St. Petersburg, RussiaWe are grateful to Dr. J.P. Arbuthnott and Dr. K. Hungerer for gifts of S. aureus -toxin, to Dr. T.B. Bolton for collaboration with patch clamped cells and to Dr. J.M. Graham for help with the preparation of Lettre cell plasma membranes. This study was supported by the Cell Surface Research Fund, Medical Research Council, Science and Engineering Research Council, UNESCO (Molecular and Cell Biology Network) and The Wellcome Trust.     

From fission to fusion: A perspective on the research that won the Nobel Prize in Physiology or Medicine, 2013

Secretion is widespread in all eukaryotic cells: all of us experience this in the course of daily life – saliva, mucus, sweat, tears, bile juice, adrenalin, etc. – the list is extremely long. How does a cell manage to repeatedly spit out some stuff without losing the rest? The answer is: through regulated vesicle trafficking within the cell. The Nobel Prize in Physiology or Medicine 2013 was awarded to Drs Randy Schekman, James E Rothman and Thomas C Südhof for their ‘discoveries of machinery regulating vesicle traffic, a major transport system in our cells’. Dr Randy Schekman and his colleagues discovered a number of genes required for vesicle trafficking from the endoplasmic reticulum (ER) and Golgi; the James E Rothman group unravelled the protein machinery that allows vesicles to bud off from the membrane and fuse to their targets; and Dr Thomas C Südhof along with his colleagues revealed how calcium ions could instruct vesicles to fuse and discharge their contents with precision. These enabled the biotechnology industry to produce a variety of pharmaceutical and industrial products like insulin and hepatitis B vaccines, in a cost-efficient manner, using yeast and tissue cultured cells.     

The Physiome Model Repository 2

MOTIVATION: The Physiome Model Repository 2 (PMR2) software was created as part of the IUPS Physiome Project (Hunter and Borg, 2003), and today it serves as the foundation for the CellML model repository. Key advantages brought to the end user by PMR2 include: facilities for model exchange, enhanced collaboration and a detailed change history for each model. AVAILABILITY: PMR2 is available under an open source license at http://www.cellml.org/tools/pmr/; a fully functional instance of this software can be accessed at http://models.physiomeproject.org/.     

Identification of two populations of biogenic amine-containing cells in the mouse lung

Summary Two distinct populations of fluorogenic amine-containing cells were observed in the lungs of nine-week old mice: one with an intense yellow emission, which possibly indicates the presence of serotonin; and one emitting a yellow-green fluorescence, which probably indicates the presence of a catecholamine such as dopamine or norepinephrine. Simultaneous identification of two different fluorogenic amine-containing cells, without pre-administration of a precursor to that amine, has not previously been reported. Such evidence of amine-containing cells demonstrated the success of the perfusion-freezing technique and established that cellular storage of fluorogenic amines does occur in vivo under normal physiological conditions. The function of such amine-containing cells has not been established; however, their location and the known physiological effects of amines would suggest regional control of ventilation/perfusion of the lung.The authors wish to thank Dr. Harry Anthony for the use of the fluorescence microscope and Dr. Robert Klemm for use of the photographic facilities. This study was supported by a grant-in-aid from the Kansas Heart Association. Contribution no. 182j, Department of Anatomy and Physiology, KAES, Kansas State University, Manhattan, Kansas 66506     

Inhibition in branched afferent neurons of the bullfrog tongue

Summary Single fibers of the bullfrog glossopharyngeal nerve give rise to several peripheral branches, each innervating separate fungiform papillae on the dorsal surface of the tongue. Extracellular electrodes were used to stimulate and record simultaneously from several papillae and from the central branch.Minor changes in centrally recorded neural output were caused by collision of action potentials originating in separate branches of a common fiber.Following an antidromic or orthodromic action potential in any branch, a series of excitability changes occured in that branch. Normal excitability was regained within 5 msec of an action potential, but was followed by a secondary decrease in excitability, which reached a minimum approximately 50 msec after the spike, and returned to normal within 200–400 msec after the spike. Subthreshold stimuli caused no depression, while doubling the stimulus strength above threshold did not enhance depression. After several spikes, both amplitude and duration of depression increased. Depression could be evoked even after the gustatory receptors were surgically removed.Post-stimulus depression in fiber branches is suggested as one source of gustatory adaptation, and may also contribute to interference between stimulating substances.The authors are particularly grateful for assistance and advice from Dr. Douglas Junge, of the School of Dentistry and Department of Physiology at the University of California, Los Angeles. The reported work was supported by NIDR Contract No. 69-2227 to Dr. Junge, and was carried out while one of the authors (JAM) held a PHS postdoctoral traineeship with the Department of Zoology, U.C.L.A., and the other (MSB) held a NIH predoctoral traineeship with the Department of Anatomy, U.C.L.A. Draughts of the paper have been read and criticized by Dr. Junge and Dr. J. P. Leader, of Auckland University.     

Atomic force microscopy of peritoneal macrophages after particle phagocytosis

The atomic force microscope was used to image peritoneal macrophages after phagocytosis of latex beads with 0.45 m in diameter and of zymosan particles. The rigidity of the phagocytosed material allowed to image the live membrane at forces below 2 nn. Repeated scanning of the membrane unavoidably caused the protrusion of the beads and increased their virtual height. The influence of fixation by glutaraldehyde on the image and the corresponding force vs. distance curves were analyzed and compared. Short treatment with Triton X-100 enabled us to identify intracellular components, such as embedded latex beads, cell nucleus and cytoskeletal strands. The data demonstrate that it is possible to image living cells if they are bolstered by stiff material.The authors wish to thank Dr. H. Oberleithner for his generous support, helpful discussions and the suggestion of Triton treatment. The authors gratefully acknowledge Dr. I. Jahns for establishing the AFM technique at the Institute of Physiology. The work was supported by the Deutsche Forschungsgemeinschaft Projekt No. La 315/4-1.     

Increased phosphorylation of tyrosine in vinculin does not occur upon transformation by some avian sarcoma viruses.

The level of phosphotyrosine in vinculin was determined in chicken embryo fibroblasts transformed by various strains of avian sarcoma virus. As previously reported (Sefton et al., Cell 24:165-174, 1981), vinculin was phosphorylated at tyrosine residues in most cultures examined, but the level varied greatly and no detectable change was found in cultures infected with Fujinami sarcoma virus or UR2 sarcoma virus. Regardless of the level of vinculin phosphorylation, the number of organized microfilament bundles was found to be decreased in all transformed cells. These results strongly suggest that tyrosine phosphorylation of vinculin is not an obligatory step in cell transformation by this class of oncogenes, nor is it correlated with the associated cytoskeletal disarray.     

Book reviews

Book reviews in this article. Encyclopaedia of Plant Physiology, New Series, Vol. 12, Part C, Physiological Plant Ecology III. Responses to the Chemical and Biological Environment Edited by O. L. Lange, P. S. Nobel, C. B. Osmond and H. Ziegler The Ethics of Environmental Concern Robin Attfield The Evolutionary Biology of Colonizing Species P. A. Parsons Ecological Genetics D. J. Merrell Phytotelmata: Terrestrial Plants as Hosts for Aquatic Insect Communities Edited by J. H. Frank and L. P. Lounibos Lake Chad — Ecology and Productivity of a Shallow Tropical Ecosystem. Monographiae Biologicae 53 Edited by J. P. Carmouze, J. R. Durand and C. Lévèque, Dr. W. Junk Guidelines for the Management of Large Mammals in African Conservation Areas Edited by A. A. Ferrar     

The Claude Bernard Distinguished Lecture. In pursuit of meaningful learning

The Bernard Distinguished Lecturers are individuals who have a history of experience and expertise in teaching that impacts multiple levels of health science education. Dr. Joel Michael more than meets these criteria. Joel earned a BS in biology from CalTech and a PhD in physiology from MIT following which he vigorously pursued his fascination with the mammalian central nervous system under continuous National Institutes of Health funding for a 15-yr period. At the same time, he became increasingly involved in teaching physiology, with the computer being his bridge between laboratory science and classroom teaching. Soon after incorporating computers into his laboratory, he began developing computer-based learning resources for his students. Observing students using these resources to solve problems led to an interest in the learning process itself. This in turn led to a research and development program, funded by the Office of Naval Research (ONR), that applied artificial intelligence to develop smart computer tutors. The impact of problem solving on student learning became the defining theme of National Science Foundation (NSF)-supported research in health science education that gradually moved all of Dr. Michael's academic efforts from neurophysiology to physiology education by the early 1980's. More recently, Joel has been instrumental in developing and maintaining the Physiology Education Research Consortium, a group of physiology teachers from around the nation who collaborate on diverse projects designed to enhance learning of the life sciences. In addition to research in education and learning science, Dr. Michael has devoted much of his time to helping physiology teachers adopt modern approaches to helping students learn. He has organized and presented faculty development workshops at many national and international venues. The topics for these workshops have included computer-based education, active learning, problem-based learning, and the use of general models in teaching physiology.     

A personal view from a long-lasting collaborator on the research strategies of Marshall Nirenberg

In this review, I summarized transition in Dr. Marshall Nirenberg’s research interests during 1970s, from a view of a long-lasting collaborator. Nirenberg switched his research filed to neurobiology after his success in deciphering genetic code and being honored with the Nobel Prize in Physiology or Medicine in 1968. His targets were to obtain genetically pure population of neurons, i.e. neuroblastoma clones, to make somatic hydrid cells, to culture neuronal and muscle cells, and to produce monoclonal antibodies against whole retinal or neuroblastoma cells. He studied neurotransmitters, receptors, cyclic nucleotides, cell differentiation, secretion, synapse formation, and chemical recognition. Especially he liked his hypothesis for opiate tolerance and dependency as a model of cellular memory. Through these studies, he seemed to devote all his time of about 50 years from 1960s to decoding brain memory processes.