Independent development of presynaptic specializations in olfactory cortex of the fetal rat

Summary Electron microscopy was used to study synaptogenesis in prepyriform cortex of fetal rat pups during early stages of synapse formation. Of special interest is the frequent occurrence of unapposed, developing synaptic specializations in axon and growth cone profiles. The location and morphology of the unapposed specializations suggests that thay are presynaptic in nature. These presumably immature presynaptic specializations are found in the lateral olfactory tract and subjacent cortex. Intermediate forms between uncontacted presynaptic specializations and definitive synapses suggest a synaptogenic sequence in which initial development of an immature presynaptic specialization begins without apposition of a postsynaptic element at that location. This implies that initiation of presynaptic development is not dependent upon postsynaptic contact and also raises the question of whether synaptic contacts could be established via presynaptic induction of postsynaptic formation.Dr. Westrum is an Affiliate of the CDMRC at the University of Washington. The research was supported in part by NIH Grants NS09678, NS17111 (NINCDS), and DE04942 (NIDR), DHHS     

Synaptic organisation and neuron microtubule distribution

Summary The microtubules in different parts of the neuron and synaptosomes were examined with respect to their stability, structure and orientation. On the basis of distribution, different labilities and differences in protofilament substructure seen by tannic acid staining, we have classified microtubules into eight major categories. Functional involvements in vesicle translocation, cytoskeletal support and the regulation of assembly/disassembly are considered.Dr. L.E. Westrum is an affiliate of the CDMRC at the University of Washington and a recipient of a Wellcome Research Travel Grant from the Burroughs-Wellcome Fund. The research was also supported in part by NIH Grants NS 09678, NS 04053 (NINCDS) and DE 04942 (NIDR), DHHS     

Activity manifestations of Hassall's corpuscles in vitro as revealed by cinematography

Summary Thymic explants from newborn rats were cultivated in Rose chambers under dialysis membranes. With the use of phase contrast, time-lapse cinematography, the following activity manifestations were observed: 1. Several corpuscles showed rotatory movements; 2. nuclear rotation was observed in some cells of the corpuscles; 3. some individual cells in the 15-day culture showed pulsatile activity which might be involved in the mechanism of the rotatory movements of the cellular aggregates; 4. the corpuscles increased in size by the addition of cells and/or by mitosis; 5. the elements at the periphery of the more mature corpuscles (7- and 9-day cultures) were viable, while the central area appeared to be composed of necrotic tissue or hyalinized material.Grateful acknowledgement is made to Dr. C. M. Pomerat for encouragement in the course of this study. Mr. Charles Raiborn aided in the preparation of cultures and Messrs. C. G. Lefeber and Robert Olson rendered indispensable assistance with the photographic work.Aided by an American Cancer Society Student Fellowship (USC-IDC) and in part by Grant No. G-14091 from the National Science Foundation administered by C. M. Pomerat.     

Marginal bundles of axoplasmic microtubules at nodes of Ranvier within muscle

Summary Using a special albumin technique, nodes of Ranvier have been examined within frog skeletal muscle, sciatic nerve and rat and frog cerebrum. Initial segments have been examined in cerebrum of frog and rat. Microtubules usually run longitudinally through these regions, but within the bare area of the intramuscular node of Ranvier, annular or helical bundles of microtubules run in a marginal band at right angles to the more centrally placed longitudinal microtubules. These nodal bare areas show a pronounced convexity and it is suggested that the annular microtubules serve to maintain this convexity during muscle contraction.Dr. Westrum is an affiliate of the CDMRC, University of Washington and a recipient of a Wellcome Trust (U.K.) Burroughs Wellcome Fund (U.SA.) Research Travel Grant. This research was also supported, in part, by NIH research Grants NS 09678 and NS 04053 from the NINCDS and DE 04942 from the NIDR, USPHS/DHEW. The authors also wish to thank Julie Barron for excellent technical assistance     

Phosphoglucose isomerase gene duplication in the bony fishes: An evolutionary history

Electrophoretic patterns of phosphoglucose isomerase (PGI) in bony fishes provide strong evidence for a model of genetic control by two independent structural gene loci, most likely resulting from a gene duplication. This model is confirmed by a comparison of certain kinetic and molecular properties of the PGI homodimers (PGI-1 and PGI-2) isolated from extracts of the teleost Astyanax mexicanus. In addition, in most higher teleosts examined, the PGI enzymes show a regular pattern of tissue distribution, with PGI-2 predominant in muscle, the heterodimer often strongest in the heart, and PGI-1 predominant in liver and other organs. An examination of 53 species of bony fishes belonging to 38 families indicates a widespread occurrence of duplicate PGI loci and an early origin of the gene duplication, perhaps in the Leptolepiformes. The apparent presence of three PGI loci in trout and goldfish exemplifies how new loci can be incorporated into the genome through polyploidization.This research was supported in part by a NSF graduate traineeship to J.C.A., by the Clayton Foundation for Research in Biochemistry (G.B.K.), by NSF Grant GB-15644 and NIH Grant GM-15769 to Robert K. Selander, and by contract AT(38-1)-310 between the University of Georgia and the U.S. Atomic Energy Commission.     

Distribution and tissue specificity of 4-aminobutyrate-2-oxoglutarate aminotransferase

A rapid and specific method for assaying 4-aminobutyrate-2-oxoglutarate aminotransferase was developed. The method was based on the selectivity of ion exchange resin and the speed of vacuum filtration. With this new method, the aminotransferase activity in various tissues has been determined as follows: brain, 10.2; spinal cord, 11.8; liver, 5.7; kidney, 4.6; heart, 0.5; lung, 0.4 nmol glutamate formed/min/mg. No activity could be detected in muscle preparations. When the aminotransferases were tested with the antibody, against the purified 4-aminobutyrate aminotransferase from brain, no difference could be detected among brain, spinal cord, and kidney preparations as judged from the results of immunodiffusion, inhibition of enzyme activity by antibody, and microcomplement fixation. It is concluded that 4-aminobutyrate aminotransferases from various tissues of the mouse are probably identical or closely related.This work was supported in part by Grant No. NS 13224 and P01 NS 12116 from the National Institutes of Health, U.S.A. and Grant from Huntington's Chorea Foundation.All correspondence should be addressed to Dr. Wu.     

Discharge and restitution of secretory material in the rat parotid gland in response to isoproterenol

Summary The sequence of morphological events occurring during discharge and restitution of secretory material in the rat parotid in response to isoproterenol administration has been studied using the electron microscope. With the dose used, discharge of secretory granules began within 5 min following injection and was complete by 40 mim. Intracellular accumulation of normal-appearing secretory material became evident at 6 hours, and restitution of resting quantities of secretory material was achieved between 12 and 18 hours after injection. Cellular events occurring during secretory discharge and restitution are discussed.This project was supported by Training Grant No. 5-Ti-GH-326 and by Predoctoral Research Grant No. 1-F1-GM-32, 528-01, National Institutes of Health. I wish to express my gratitude to Dr. Henry S. di Stefano under whose directorship this project was carried out.     

Directionally selective motion detecting units in the optic lobe of the honeybee

Summary We have found four classes of neurons in the honeybee optic lobe. These neurons respond to changes in light intensity and selectively to movement of objects within the entire acceptance angle of a compound eye. We suggest that these neurons are part of the neural system that controls flight, for example the optomotor response. Properties of these units are described in this paper. To our knowledge this is the first report of recording from interneurons of the honeybee.We thank Mrs. B. Hsei and Mrs. D. Hodgetts for technical assistance. Bees to establish the wild-type colony were given by Dr. P. Wells, Occidental College; bees to establish the white-eyed mutant colony were given by Dr. H. Laidlaw, University of California at Davis, California.This research was supported by National Institutes of Health, U.S.P.H.S. Grant NB03627 to Dr. G. D. McCann (CIT), and A.F.O.S.R. Grant 70-1869 to LGB.One of us (WK) is indebted to the Commitee on International Exchange of Persons, Washington D.C., for making available a Fulbright Travel Grant. WK also thanks Dr. G. D. McCann for the invitation to the California Institute of Technology.     

Ultrastructural differentiation during embryonic Drosophila myogenesis in vitro

Summary Cultures of embryonicDrosophila melanogaster cells were examined by electron microscopy and events in myogenesis were recorded. Thick and thin myofilaments, T-tubules and sarcoplasmic reticulum all appeared at about the same time, 10.5 hr. This was about 5 hr after the final division of myoblasts and about the time that muscle cells were elongating, aligning and fusing. Sarcoplasm typical of insect muscle was detected by 18.5 hr, as were myotendonal and tendocuticular junctions. Two populations of myocytes were detected, the cytoplasm of one more electron-dense than the other. The only previous report of myofibrilogenesis in invertebrate embryos had described novel mechanisms. InDrosophila embryonic material, however, the sequence of myofibrilogenesis resembled that in post-embryonic insect or vertebrate material. Mrs. Pilar Toribio-Fiorio provided excellent technical assistance, and Patricia Minter, the secretarial expertise. This investigation was supported, in part, by NIH Grant NS9330 and the James Douglas Research Fund to Robert L. Seecof and NIH Grant No. 1 RO1 CA17223-01 to Raymond L. Teplitz.     

Synapses in the cerebral ganglion of adult Ciona intestinalis

Summary Electron microscopy of the synaptic morphology of synapses in the cerebral ganglion of the adult ascidian (sea squirt) Ciona intestinalis reveals that the synapses are restricted to the central neuropil of the ganglion. Many of the synapses show a polarity of structure such that pre and post synaptic parts can be identified. The vesicles in the presynaptic bag are of two main diameters 80 and 30 nm respectively. The large vesicles have electron dense contents that vary both in their capacity and dimensions.The pre and postsynaptic membranes are more electron dense than the surrounding membranes, but they are only slightly thicker. Both the pre and post synaptic membranes have electron dense dots some 10 nm in diameter associated with their cytoplasmic surfaces. Sometimes the presynaptic membrane has larger peg-like projections between the vesicles. Associated with the post synaptic membrane are tubules some 10 nm in diameter. These tubules may be the dots cut obliquely.The synaptic cleft material is more electron dense than the surrounding intercellular material, and in it there is a dense line made up of granules about 3–5 nm in diameter. This dense line is usually mid way between the pre and post synaptic membranes, but may be nearer the postsynaptic membrane.No tight junctions between adjacent nerve process profiles have been observed.I wish to thank Professors J. Z. Young, F. R. S. and E. G. Gray for much advice and encouragement, also Dr. R. Bellairs for the use of electron microscope facilities and Mr. R. Moss and Mrs. J. Hamilton for skillful technical assistance.     

The fine structure of sensory receptor processes in the auricular epithelium of the planarian,Dugesia tigrina

Summary The marginal epithelium of the lateral auricles of the planarian, Dugesia tigrina, includes a cell type with surface cilia and microvilli, a basal nucleus, and dense cytoplasm containing secretory vacuoles, Golgi elements, mitochondria and ribosomes. Through channels within the epithelial cytoplasm, cellular processes, interpreted as extensions of neurosensory receptor cells located in the subepidermis, project to the surface. The receptor processes, containing microtubules, mitochondria, vesicles and an agranular tubular reticulum, project beyond the epithelial cell surface; one or two cilia each emerge from a basal body in the apex of the projection. Close to the point of emergence to the epithelial surface, each cylindrical receptor process is surrounded by a collar-like septate junction between adjacent plasma membranes. The cilia of the projections differ from those of the epithelial cells in diameter, density of matrix and in the banding patterns of the rootlets. A few projections appear with the apex and basal body retracted below the epithelial surface. The possible function of these ciliated processes in sensory reception is discussed.This work was supported by Grant No. SO 1 FR 5369 from the U.S. Public Health Service to the University of Illinois at the Medical Center.I thank Dr. J. P. Marbarger, Director of the Research Resources Laboratory, for use of the electron microscope facilities, Miss Irena Kairys for technical help, Miss Marie Jaeger for assistance with photography, and Mr. Robert Parshall for the drawing.To Professor Arthur Wagg Pollister, I respectfully dedicate this article on the occasion of his retirement from Columbia University.     

Comparative evaluation of three in vacuo dessication procedures on bacterial cultures

The paper presents results obtained for the bacterial cultures preservation (E. coli ATCC 25 922 and S. aureus Wood) by three in vacuo desiccation procedures: freeze-drying (lyophilization or cryo-desiccation at eutectic zone), cryo-desiccation above eutectic zone and direct drying. It has been in view: the survival of liquid cultures as reported to the desiccation procedure per se, the loss of viability of desiccated cultures stored in refrigerator for at least one year and the residual moisture of desiccated cultures. For 3 batches there has been applied the accelerated thermal degradation test. Employing the same protective medium for both cultures, E. coli cultures prove to be more easily affected by lyophilization and cryo-desiccation above eutectic zone as compared to S. aureus cultures, fact that may be due to the differences between the wall structures of G--bacteria and G+ bacteria, respectively. During storage, E. coli and S. aureus cultures proved a quite similar loss of viability. The residual moisture content was quite similar for both E. coli and S. aureus cultures exposed to the same in vacuo desiccation procedure. The lyophilization and the cryo-desiccation above eutectic zone, as compared to direct drying, yielded superior results. The accelerated thermal degradation test provides only informative results, partially confirmed by viable counts determined at stated intervals of storage time in the refrigerator.     

Evaluation of methods for determining 6-hydroxydopamine cytotoxicity

Summary The toxic effects of 6-hydroxydopamine on the human neuroblastoma cell line SK-N-SH-SY5Y (SY5Y) and the Chinese hamster ovary (CHO) cell line were measured with five viability assays. Four of the assays (attachment efficiency, plating efficiency, amino acid incorporation into acid-precipitable proteins, and Trypan Blue dye exclusion) showed higher drug susceptibility in SY5Y cells than CHO cells. Only growth inhibition (proliferation index) gave results indicating greater sensitivity in CHO cells. Over a time span of 48 hr, injured cell populations lost vital functions in the following order: attachment ability, amino acid incorporation, proliferative capacity, and dye exclusion. Recovery of each of the functions occurred in sublethally injured populations. Monitoring the extinction and recovery of vital functions permitted the accurate determination of a drug concentration (30 μg/ml) selectively toxic for SY5Y cells. A strong correlation was noted between relative values for amino acid incorporation 3 hr after drug treatment, attachment efficiency at 24 hr, and dye exclusion at 24 and 48 hr. We concluded that Trypan Blue dye exclusion and amino acid incorporation were suitable methods for comparing the effects of cytotoxins on different cell lines, provided they were performed at the appropriate time after treatment with the toxin. The combined techniques yield both population and individual cell data, are simple to do, and are applicable to nondividing cell populations. This work was supported by an NIH National Research Service Award GM07204 to E. T. C., a gift from the Lola-Wright Foundation, NINCDS Grants NS14034 and NS15234, Robert Welch Grant H698, and an RCDA (NS00213) to J. R. P.     

Nuclear and cytoplasmic differentiation in developing sperm of the crayfish,Cambaroides japonicus

Summary In the present electron microscopic study of spermatogenesis in the crayfish, Cambaroides japonicus, it was possible to clarify several aspects of the unusual differentiation which leads to the production of an aflagellate sperm. The centriole is followed from the metaphase of the second spermatocyte division to the time at which, in the nearly mature sperm, it appears to disintegrate. It has no connection with the acrosome but in the late spermatid and maturing sperm it is found randomly oriented among the convoluted membranes of the filamentous endoplasmic reticulum.There appears to be a close association of mitochondria with the developing acrosomal vesicle. Typical mitochondria, however, are not present after the late spermatid stage of development. It is suggested that the complex lamellar bodies associated with the nuclear envelope in the late stages of spermatogenesis may be related to mitochondria for these lamellar bodies resemble the complex mitochondria found in the adjacent nutritive cells.The development of the acrosome has been traced from an aggregate of dense granules which first appear in the interzonal spindle region and are later segregated at one side of the cell after the second spermatocyte division. As differentiation proceeds, tubular elements appear and disappear within the acrosome, while somewhat later, fibrous elements appear in the matrix. In the mature acrosome, the fibrous elements remain only adjacent to the granular periphery of the acrosome and the core again becomes homogeneous.No typical Golgi complex is found in these cells at any time during their differentiation.In the maturing sperm the development of the arms of the nucleus was studied. Preceding the differentiation of the arms a coarse fibrous material develops in the periphery of the nucleus. It is shown that the fibrillar material in the matrix of the arms is in continuity with the fibrillar material in the matrix of the nucleus proper.Supported in part by Grant No. B 2314 of the National Institute of Neurological Diseases and Blindness, U.S. Public Health Service.Predoctoral Research Fellow of the National Institute of Neurological Diseases and Blindness, U.S. Public Health Service.     

Time of replication of ARS elements along yeast chromosome III.

The replication of putative replication origins (ARS elements) was examined for 200 kilobases of chromosome III of Saccharomyces cerevisiae. By using synchronous cultures and transfers from dense to light isotope medium, the temporal pattern of mitotic DNA replication of eight fragments that contain ARSs was determined. ARS elements near the telomeres replicated late in S phase, while internal ARS elements replicated in the first half of S phase. The results suggest that some ARS elements in the chromosome may be inactive as replication origins. The actively expressed mating type locus, MAT, replicated early in S phase, while the silent cassettes, HML and HMR, replicated late. Unexpectedly, chromosome III sequences were found to replicate late in G1 at the arrest induced by the temperature-sensitive cdc7 allele.     

Methods for the study ofin vitro immunization of mouse spleen cells

Conclusion We have reviewed some of our experiences in developing techniques for studying the functions of the cells of the immune system. It is quite clear that much remains to be done. Improvements in the culture system are needed to permit cells to be grown for longer durations and at lower cell concentrations. The important effects of fetal calf serum should be defined. More sophisticated methods for separating cells into distinct functional populations must be developed. New assays for identifying other functions of the cells, particularly a method for directly assaying the number of precursor cells in a population, are needed. When these techniques are applied to the study of immune cells, further facts should be learned which will permit the development of significant, testable hypotheses on the function and relationships of the cells of the immune system. This is publication No. 298 from the Department of Experimental Pathology, Scripps Clinic and Research Foundation, La Jolla, California 92037. This work was supported in part by U.S.P.H.S. Grant 7007 and in part by American Cancer Society Grant E-395. Dr. Mishell is supported by American Cancer Society Grant E-395. Dr. Dutton is supported by a Dernham Fellowship of the California Division, American Cancer Society (No. D-100). Dr. Raidt is supported by United States Public Health Service Postdoctoral Fellowship No. 7-F2-A1-31,590.     

Adenylate kinase deficiency and malignant hyperthermia

Summary In a report of two patients who died of malignant hyperthermia, muscle adenylate kinase deficiency was identified in the father and brother of the deceased. To determine if this enzyme deficiency was a biochemical marker for susceptibility to malignant hyperthermia, we measured adenylate kinase in muscle of three survivors of malignant hyperthermia (MH) and five relatives of survivors of MH attacks with positive caffeine contracture tests. Neither the activity nor the electrophoretic mobility of adenylate kinase differed from four control values. The results show that muscle adenylate kinase deficiency is not a biochemical abnormality shared by all individuals susceptible to malignant hyperthermia.This work has been supported by grants from Muscular Dystrophy Association of America, NIH (NS 11766)Dr. Cerri is recipient of a postdoctoral fellowship from Muscular Dystrophy association and Dr. Willner is recipient of a Teacher Investigator Award from NINCDS     

Adaptive cardiovascular modifications in the western chipmunks genusEutamias

Summary Although cutaneous type I and type II mechanoreceptors in the cat respond at progressively higher frequencies to increasingly rapid skin indentations of suprathreshold intensity, their thresholds are not lowered when these more rapid stimuli are applied. Since these receptors do not selectively detect rapid stimuli of small amplitude, even though they respond much more vigorously to a suprathreshold stimulus that is rapid, different parameters of the stimulus are signalled depending on whether it is near threshold or clearly suprathreshold.This work was supported by grant GB42643 from the National Science Foundation and by grants NS08769, NS07938 and NS05244 from the U.S. Public Health ServiceThe authors thank John Fisher, Gary Frederickson, Tom O'Leary, Robert Perry, and Jane Burgess for their valuable help.     

Sympodiomyces gen. n., a yeast-like organism from southern marine waters

Sympodiomyces gen. n. is described with the single speciesSympodiomyces parvus sp. n. The distinguishing characteristic of this yeast-like genus is the method of asexual reproduction: conidia are produced on a conidiophore that develops sympodially. A sexual stage has not been observed, therefore the genus is placed among the Fungi Imperfecti, family Cryptococcaceae.Contribution No. 1364 from the Rosenstiel School of Marine and Atmospheric Science, University of Miami, Florida.The authors gratefully acknowledge Dr. Jan Kohlmeyer, Univ. of North Carolina, Morehead City, North Carolina; Dr. R. T. Moore, North Carolina State Univ. at Raleigh; Dr. H. J. Phaff, Univ. of California at Davis; Miss W. Ch. Slooff and Mr. D. Yarrow, CBS, Delft, Netherlands; Dr. K.Tubaki, Institute for Fermentation, Osaka, Japan; and Dr. J. A. von Arx, C.B.S., Baarn, for examining cultures ofS. parvus. Dr. D. P. Rogers, Univ. of Illinois, Urbana, Ill, prepared the generic Latin diagnosis. Mr. Steven Y. Newell and Mr. A. Weiner, Univ. of Miami, assisted in obtainingEltanin collections. This study was supported by the National Science Foundation through the Office of Antarctic Programs Grant No. GA 13675.     

Formation,transport, and storage of ribonucleic acid containing structures in oocytes of Acheta domesticus (Orthoptera)

Summary Oocyte development of Acheta domesticus was investigated morphologically and cytochemically. The studies demonstrated a size decrease and final disappearance of a large extrachromosomal DNA body in the nuclei as the cells proceeded through the diplotene stage of meiosis. The body was surrounded by fascicles of RNA containing material. This material remained within the nuclei in individual packets after the DNA body was no longer detectable. An active nucleo-cytoplasmic migration of RNA was seen prior to the disappearance of the DNA body. After the disappearance of the body very little migration was detected. Evidence was presented to demonstrate the ribosomal nature of this migratory RNA. The RNA packets remaining in nuclei of cells arrested in the diplotene stage of oogenesis functioned as storage depots for ribosomal RNA.The authors acknowledge the technical assistance of Miss Agnes Cralley. Dr. D. Ammermann, Zoologisches Institut, Tübingen, W. Germany, provided the animals used in this study. — This work was supported in part by a Health Research Services Foundation Grant No. J-1 and in part by U.S.P.H.S. Grant No. 7-FZCA-23,971-O1A1.