Tissue variability of the phosphotransferases adenylate kinase (EC: 2.7.4.3.) and pyruvate kinase (EC: 2.7.1.40.)

Summary Studies of the tissue variability of human AK and PK are reported. Homozygous probands of phenotype AK 1, show five electrophoretic positions with AK activity in different tissues and six positions with PK activity. In one of the 20 probands studied the brain, not however any other tissue, revealed a different zymogram. It can be followed therefore that different isozymes can be present in different tissues.Head: Prof. Dr. Dr. H. BaitschSupported by the Deutsche Forschungsgemeinschaft.     

Evolution of bioengineering at UCSD: opening new vistas

Before this, the field of bioengineering refers to biomedical engineering of prosthetic devices in physiology. In addition to exciting applications of engineering principles, UCSD Department of Bioengineering began to extend the notion of engineering models of physiological systems to physiological processes. This led to a conceptual shift in the discipline and contributed to the areas of tissue and physiological process engineering. In 1988, Dr. Shu Chien and Richard Skalak joined UCSD to begin research and education on cellular and molecular bioengineering, especially, mechanobiology. Dr. Fung and Dr. Skalak initiated the new field of tissue engineering. These two decades of evolution of bioengineering and its growth across the country was spearheaded by the Whitaker Foundation, whose leitmotif was the building of bioand biomedical engineering across the country. We have garnered other accomplishments in the following fields: regenerative medicine; bioinspired artificial extracellular matrices; flexible bioelectronics and tatoos; cells show how to synchronize biological clocks; and systems medicine.     

Meeting report: Human fetal tissue transplantation research panel

Summary On September 14 through 16, 1988, a meeting on the use of human fetal tissue in transplantation was held at the National Institutes of Health, Bethesda Maryland, USA. The meeting sponsored by NIH for the Human Fetal Tissue Transplantation Research Panel, a consultant group to the Advisory Committee to the Director. The consultant group was convened to deal with the scientific, judicial and moral questions associated with research involving transplantation of human fetal tissue obtained after induced abortions. The first day of the meeting was devoted to presentations addressing scientific issues. Included among the speakers was Dr. Lars Olson, Professor of Neurobiology, Karolinska Institute, Stockholm, who described the use of transplanted human fetal tissue in the treatment of patients with Parkinkson's disease and Dr. Eugene Redmond, Professor of Psychiatry, Yale University School of Medicine, who showed results of work with transplantation of tissue to correct induced Parkinson-like disease in monkeys. Other speakers addressed the present, past or potential use of fetal tissue in the treatment of diabetes, immune disorders, and other diseases, as well as the use of fetal cells in the production of biologicals. At the conclusion of the meeting the panel did not recommend that research be halted on fetal tissue within the context discussed, although the recommendation of the committee is not binding, and an additional assembly of the panel will probably occur before the final recommendation to an NIH advisory committee is made in November. Other meetings on this subject include a meeting on the use of fetal tissue sponsored by the American Association of Tissue Banks, March 6–7, 1989, in Washington D. C. (Crystal City) and a meeting June 10, 1989, the day before the annual meeting of the Tissue Culture Association, USA, in Orlando, Florida, on fetal cells and ownership of cultured cells and products derived from clinical specimens. Following are statements to the Human Fetal Tissue Transplantation Research Panel presented September 14, 1988, by Dr. David Barnes, Associate Professor of Biochemistry and Biophysics in the Environmental Health Sciences Center at Oregon State University, USA, who was asked to address for the panel recent advances in cell culture related to fetal tissue, and Dr. Robert E. Stevenson, Director of the American Type Culture Collection, President of the Tissue Culture Association, USA, and Chairman of the Committee on Cells and Tumors of the American Association of Tissue Banks.     

Occurrence of Falcarinol and Falcarindiol In Tomato Plants after Infection with Verticillium albo-atrum and Characterization of Four Phytoalexins by Capillary Gas Chromatography-Mass Spectrometry

Falcarinol and falcarindiol were isolated from tomato vascular tissue infected with Verticillium albo-atrum and identified. Separation and characterization of trimethylsilyl derivatives of four tomato phytoalexins could be obtained by capillary gas chromatographymass spectrometry. We are most grateful to Dr. P. J. G. M. de Wit , Agricultural University, Wageningen, to Dr. D. T. Coxon , Food Research Institute, Norwich and to Dr. M. S. Kemp , Long Ashton Research Station, Bristol for making their analytical data available for us. Also thanks are due to Miss J. I. Liem , Mr. G. Verweij and C. Loriaux for their assistance.     

Effects of potassium,lanthanum and black widow spider venom on miniature synaptic potentials in theTorpedo electroplax

Summary Using a method of focal drug application it is demonstrated that high potassium concentration, lanthanum, and black widow spider venom accelerate spontaneous transmitter release inTorpedo electric tissue.This investigation was supported by the Deutsche Forschungsgemeinschaft (Sonderforschungsbereich 138). Thanks are due to Dr. R. Martin and the staff of the Stazione Zoologica, Naples, for supplyingTorpedo, and Dr. N. Frontali, Rome, for a gift of frozen black widow spiders.     

A tribute to Dr. Gordon Hisashi Sato (December 24, 1927–March 31, 2017)

Gordon H. Sato, an innovator in mammalian tissue culture and integrated cellular physiology, passed away in 2017. In tribute to Dr. Sato, In Vitro Cellular and Developmental Biology—Animal presents a collection of invited remembrances from six colleagues whose associations with Dr. Sato spanned more than 40 years. Dr. Sato was a past president of the Tissue Culture Association (now the Society for In Vitro Biology), editor-in-chief of In Vitro Cellular and Developmental Biology (1987–1991), and the recipient of the lifetime achievement award from the Society for In Vitro Biology (2002). He was elected to the US National Academy of Sciences in 1984.     

Quantitative electron microscopic studies on the innervation of the human thymus

Summary Quantitative electron microscopic studies have been carried out on the human thymus. According to the equation L _v =(2n)/F (Hennig, 1963) we have calculated that there is less than 0.204 mm nerve per 1 mm³ thymus tissue inside the blood-thymus-barrier (level of significance of 0.95). This result is compared to the degree of innervation in brown adipose tissue, which contains more than 160 mm nerve per 1 mm³ tissue. The biological significance of the paucity of neuronal elements in the thymus is undetermined.We are much obliged to Dipl. Ing. Dr. A. Hennig for his advice in the mathematical evaluation of our results.We are also indebted to Dr. med. A. Krug (Chir. Universitätsklinik Kiel) for human thymus material.This investigation was supported by the Deutsche Forschungsgemeinschaft.     

Lactation physiology: A ruminant animal perspective

Summary Importance of peripubertal mammary development as a foundation for subsequent mammary growth and milk production was discussed. Morphological differences in peripubertal mammary growth in rodents and ruminants were described. The relevance of tissue interactions and association with hormones and growth factors in mammary development were delineated. Data from specific studies with ruminant mammary parenchyma were outlined for comparison with rodent studies. It is concluded that the wholesale extrapolation of data from rodent studies to explain udder development is inappropriate. Lastly, recent data from experiments with culture of mammary explants from bulls is described. Pragmatically, these data suggest that responses of mammary tissue from bulls might provide a means for early selection of superior sires or provide a unique model to study tissue interactions in udder development.It has been a pleasure for me to have the opportunity to prepare this paper in honor of Dr. Stuart Patton on his 70th birthday. Dr. Patton, one of the founders of the Gordon Conference on Mammary Gland Biology, had the vision to bring together the variety of workers interested in the mammary gland and drive to foster wide ranging collaborations.     

Elimination of Mycoplasma from various cell cultures

Elimination ofMycoplasma orale-I from chronically infected cell lines was achieved either by treatment with a mixture of antibiotics in a hypotonic solution, or with 10 vol % of anti -M.orale rabbit serum in tissue culture medium. The latter treatment was preferable in most cases, as it was practically harmless to the cells. Inactivation of this antiserum had no effect on its potency. The antibiotic-hypotonic treatment was rather destructive, but to a different degree for the various cell cultures. Both methods were equally useful for the treatment of a monkey kidney cell line contaminated with a mycoplasma strain related toM.hyorhinis. The available anti -M.hyorhinis rabbit serum was toxic for the monkey cells when not inactivated. The potency of the antiserum was rather low and even lower after inactivation. However, prolonged treatment successfully eliminated the mycoplasma. Pre-incubation of the inactivated anti -M.hyorhinis serum with tissue culture medium to which 10% non-inactivated calf serum had been added, favoured the elimination of the mycoplasma.During the treatment of contaminated cell cultures with single antibiotics a strain related toM.hyorhinis became resistant to chlortetracyclin.M.orale- I was found to be resistant to various single antibiotics.We are grateful to Professor Dr. A. Ch. Ruys (University of Amsterdam) and Dr. R. H. Leach (Mycoplasma Reference Laboratory, London) for helpful discussions and for identifying some of our mycoplasma strains; Dr. Leach also for kindly supplying us with his G. D. L.-strain. We thank Dr. H. Cohen and Dr. A. C. Hekker for their criticism and Mr. N. L. M. van Zwetselaar for his accurate technical assistance.     

Brassinolide-Induced Elongation of Inner Tissues of Segments of Squash (Cucurbita maxima Duch.) Hypocotyls

Brassinolide (BR) stimulated elongation of etiolated squashhypocotyl segments with outer tissues removed, as well as thatof unpeeled segments, while IAA has no effect on peeled segments.BR changed the mechanical properties of cell walls of the innertissue. The inner tissue is probably the target tissue in BR-inducedelongation. ¹Dr. Susumu Kuraishi died in 1993.     

Identification and distribution of profilin in tomato (Lycopersicon esculentum Mill.)

Profilin is a G-actin monomer-binding protein which has been shown to participate in actin-based tipgrowth of animal cells. The abundance of profilin in pollen and its occurrence in several vegetable foods raises the question of the role of profilin in plants. First, its distribution throughout various parts of the plant needs to be determined. This paper describes observations on the presence of profilin in the tomato plant (Lycopersicon esculentum Mill.). The distribution of profilin in flower buds, stems, leaves, roots, and fruits of tomato was determined by immunoblotting and by tissue printing, showing that profilin is present in most if not all parts of the tomato plant.We gratefully acknowledge the help provided by Dr. A.T. Jagendorf and the donation of tomato seeds and maize pollen by N. Eanetta and Dr. M. Smith, respectively. The use of Dr. R. Wayne's SZH ILLD dissecting microscope is gratefully acknowledged. This work was aided by helpful discussions with C.S. Combs, Dr. C.A. Conley, and Dr. J. Andersland. This work was supported by a Hatch grant and NRI Competitive Grants Program/USDA 94-37304-1046 to MVP. This material is based upon work supported under a National Science Foundation Graduate Research Fellowship to DWD.     

Further Experimentation with A New Differential Staining Method for Connective Tissue Combined with the Ordinary Hematoxylin-Eosin Stain

There appeared recently in the University of Oklahoma Bulletin an article by Jos. M. Thuringer¹ describing a new differential staining method for connective tissue. Dr. W. J. Baumgartner suggested to the writer that she undertake to stain a series of sections using the method described by Mr. Thuringer. We wished especially to test this method in order to determine if it could be introduced into the course in technic as one of the routine stains for connective tissue.     

Dr. David Rimm is interviewed by Feras Akbik

Dr. David Rimm, MD PhD, is a professor of Pathology at the Yale University School of Medicine specializing in developing quantitative, diagnostic techniques. His lab recently engineered a fluorescence-based algorithm, Automated Quantitative Analysis (AQUA), to analyze tissue microarrays in the hope of moving toward personalized medicine and diagnoses.     

BUCHBESPRECHUNGEN

K oepcke , H.-W.: DieLebensformen(Grundlageneiner universellgültigenbiologischen Theorie) . Bd. 1. l. Teil: Grundbegriffe, 1971;
M athews , M. B.: Connective tissue. Macromolecular structure and evolution. Molecular biology, biochemistry and biophysics. Vol. 19. Ed. by A. K leinzeller , G. F. S pringer AND H. G. W ittmann .
Formen sozialen Verhaltens. Von Prof. Dr. N ikolaas T inbergen , Oxford. Übersetzt von Prof. Dr. O tto K oehler , Freiburg i. Br. 3. Auflage. 1975.     

Substrate dependence of cell migration from explanted neural tubes in vitro

Summary Embryonic chick neural tubes containing neural crest cells were cultured in vitro on tissue culture plastic and collagen. Two parameters, the time of onset of cell migration from the neural tube and the rate of movement of the cell front away from the neural tube explant, were determined. On collagen, cell migration consistently began after four to six h in vitro, about five h prior to the onset of cell migration on tissue culture plastic. The identity of the migrating cells as neural crest cells is established by their eventual differentiation into melanocytes. Ablation experiments reveal that collagen also causes the early onset of migration of cells not of neural crest origin. These results provide in vitro support for the idea that extracellular materials may alter cell migratory behaviour in morphogenesis.Supported by PHS grant HD-05395 to Dr. James A. Weston and NIH Predoctoral Research Fellowship GM-47392 to Gerald D. Maxwell. The author thanks John Pintar for his permission to quote unpublished observations on the neural crest films and for helpful discussion, and Dr. Peter H. von Hippel for the gift of icthyocol     

Tissue stabilisation during histochemical reactions: The use of collagen polypeptides

Summary The incorporation of polyvinyl alcohol into the incubation medium prevents the loss of material from unfixed tissue sections during incubation. Polypeptides, derived from the partial degradation of collagen, are equally effective in retaining this material; at the same time they offer certain advantages over polyvinyl alcohol as tissue stabilisers.I wish to thank Mr. G. Frost for providing the polypeptides and Dr. J. Chayen for his interest and advice. I am grateful to the Medical Research Council for a grant and the Arthritis and Rheumatism Council for Research for general support.     

Vaccine could not have been prepared in Stanleyville

In Stanleyville, at the time of vaccination campaigns, tissue cultures were primitive, experimental and used solely for diagnostic purposes. Production of vaccine was impossible to carry out. A few chimpanzee kidneys were minced and sent to Philadelphia as part of the hepatitis experiments of Dr Deinhardt. Vaccine was never handled in my laboratory and contamination with chimpanzee cells was not possible.     

Regeneration in the central nervous system of a pulmonate mollusc,Melampus

Summary The left cerebral ganglion was ablated from 72 anesthetized, adult Melampus bidentatus (Mollusca: Pulmonata). Skin incisions were well healed and normal feeding and locomotion observed four days after surgery. Dissections of animals sacrificed weekly showed that most nerves and connectives regrew within 30 days, attaching to the swollen end of the major labial nerve. The enlarged end of this nerve later developed into a distinctive bud; some of these buds contained cell bodies as soon as 42 days after surgery. As the first known report of central nervous tissue regeneration in molluscs, this study points to the need for controls in experiments involving section or ablation of nervous tissue in molluscs.I am grateful to Dr. W.D. Russell-Hunter for his guidance in the course of this work. Support was principally provided by a grant from the National Science Foundation to Dr. Russell-Hunter (Research Grant No. GB-36757 continued as BMS-72-02511-A01)and by two successive grants to the author from the Theodore Roosevelt Memorial Fund of the American Museum of Natural History, New York     

The antigenicity of regenerating tail tissue in the newt Diemictylus viridescens

Young adult male rabbits were inoculated with antigens prepared from regenerating (blastema stage) and nonregenerating tail tissues of the newtDiemictylus viridescens. Blood was collected from these rabbits after six weeks of semiweekly injection, two weeks of respite, and two more weeks of injections. A Freund adjuvant was added to the antigen preparations at the time of injection in order to elicit the anamnestic effect.Ouchterlony agar diffusions of the newt antigen preparations vs. the rabbit antisera were carried out. The resulting patterns of precipitation bands were compared and photographed.The strongest precipitation reactions of a given series were those between the antigen preparations made from nonregenerating tissue and their homologous antisera. The weakest reactions occurred between regenerating tissue antigens and regenerating tissue antisera. The strength of the antigen-antibody reactions was judged by the number of bands appearing in the diffusion plate and by the distinctness of these bands. Reactions of intermediate strength occurred between regenerating antigens and nonregenerating antisera, between nonregenerating antigens and regenerating antisera, and between antigens and antisera of different series.The loss of antigenicity during the blastemal period was considered to be related to the destruction of tissue in the wound areas at this time, and to indicate a quantitative rather than a qualitative loss of protein in regenerating tissue.This work is taken from data submitted to the Department of Biology of Fordham University in partial fulfillment of the requirements for the degree of Doctor of Philosophy, and was supported in part by a grant from the New York City Cancer Committee of the American Cancer Society.The author acknowledges his indebtedness to Dr.Alexander Wolsky of Fordham University, under whose direction this investigation was carried out, and Dr.John J. Corbett of Manhattan College and Lederle Laboratories.