Social interactions of monkeys reared in a nuclear family environment versus monkeys reared with mothers and peers

Four-year-old laboratory-born rhesus monkeys that had been reared in a nuclear family social environment consisting of mothers, fathers, siblings, peers, and other adults of both sexes were permitted to interact in various combinations with equal-aged monkeys that had been reared in an environment consisting of only mothers and peers. It was found that in most interaction sessions nuclear family subjects exhibited significantly higher levels of dominance and activity behaviors and significantly lower levels of submissive and passive behaviors than the mother-peer-reared subjects. These differences were not evident when subjects were tested within their own rearing groups. The significance of the results with respect to previous and future studies of social development in differential social environments is discussed.This research was supported by grant No. MH-11894 from the National Institute of Mental Health to the University of Wisconsin Primate Laboratory, by the Grant Foundation, and by grant No. RR-0167 from the National Institutes of Health to the University of Wisconsin Primate Research Center.     

Structure and development of sieve areas in leaf veins ofWelwitschia

Summary The sieve areas inWelwitschia are essentially similar to those of coniferous sieve cells, consisting of groups of plasmalemma-lined pores, which are joined in the middle of the wall by a median cavity. The median cavity contains membranes which apparently are connected with aggregates of endoplasmic reticulum bordering the sieve areas. The median cavity is formed through union of smaller median enlargements, the median nodules, each initially associated with a plasmodesma, during perforation of the young sieve area. Callose platelets are not associated with developing pores. All fully-developed pores were lined with callose. The sieve cells are connected with only one other cell type, the albuminous cell. On the sieve-cell side of the wall these connections are similar to sievearea pores, on the albuminous-cell side to plasmodesmata. These connections are also characterized by median enlargements.This work was supported in part by a grant from the South African Council for Scientific and Industrial Research and in part by the U.S. National Science Foundation (GB 31417).     

Use of commercial serum replacements for the culture of insect cells

Summary Two commercially available serum replacements developed for use in the culture of hybridoma and other mammalian cells were tested for their suitability as replacements for fetal bovine serum in insect cell culture medium. CPSR-1 and CPSR-3 both supported growth of the insect cell line IPLB-SF-21AE. CPSR-3 supported adequate growth, but cells in medium supplemented with CPSR-1 grew much slower and achieved only about half the final cell density of either FBS or CPSR-3 supplemented medium. This work was supported in part by grant 187159 from the Juvenile Diabetes Foundation and BRSG RR05876 from the National Institutes of Health, Bethesda, MD.     

Global stability in a chemostat with multiple nutrients

We study a single species in a chemostat, limited by two nutrients, and separate nutrient uptake from growth. For a broad class of uptake and growth functions it is proved that a nontrivial equilibrium may exist. Moreover, if it exists it is unique and globally stable, generalizing a result in [15]. supported in part by NSF grant DMS 0342153. supported in part by NSF grant DEB-0083566 and the Andrew W. Mellon Foundation. supported in part by USAF grant F49620-01-1-0063 and NSF grant CCR-0206789. Part of this work was carried out when P. De Leenheer was a post-doctoral fellow at DIMACS, Rutgers University, supported in part by NSF grant EIA03-331486 and USAF grant F49620-01-1-0063.     

Ovulation and the mechanism of follicle rupture

Summary The effects of penicillin and chlortetracyline HCl on the fine structure of the intracellular symbiotes of the pea aphid were studied in an attempt to remove the symbiote population. High penicillin concentrations, 1% and 0.1%, caused symbiote breakdown but were toxic and/or repellent to the aphids; at 0.1% specific effects were observed on the symbiotes' cell walls. After the use of 0.01% penicillin in the aphid diet, the symbiotes had abnormal cell walls and were abnormally dilated; however, symbiote division and transmission from one aphid generation to the next seemed unaffected and the aphids appeared normal. Aphids fed 0.1% chlortetracycline failed to reproduce. After 7 days, their symbiotes were found to break down at a high rate but aphid mitochondria were also adversely affected at this stage. Following 0.002% chlortetracycline, the aphids produced aposymbiotic progeny with apparently normal mitochondrial populations; these larvae failed to develop.Research supported by the College of Agricultural and Life Sciences, University of Wisconsin, and by a research grant (GB 31904 X) from the National Science Foundation.     

The stem and leaf lectin of Dolichos biflorus L., previously thought to be cell wall associated,is sequestered in vacuoles

Post-embedding immunogold labeling has shown that the DB58 lectin is sequestered in vacuoles. Previous evidence indicating that a significant fraction of the DB58 lectin is cell wall associated is shown to be in error.Abbreviations PBS 10 mM sodium phosphate, pH 7.1, 154 mM sodium chloride - TBS 20 mM Tris base, pH 7.6, 137 mM sodium chloride We thank Dr. Mary Alice Webb for sharing her electron-microscopy expertise. This work was supported by National Science Foundation grant DCB-9004967 (M.E.E.) and a University of California, Davis, Jastro-Shields fellowship (T.W.B.).     

Autoradiographic and microspectrophotometric studies of DNA synthesis in excised tobacco pith tissue

Summary Pith tissue was cultured on modified White’s nutrient medium supplemented, except for controls, with 2 mg/l of IAA and/or 0,5 mg/l of kinetin. For autoradiographs sections were used from tissue grown on medium containing tritiated thymidine. Nuclear DNA contents (Feulgen) were measured by the microspectrophotometric two-wavelengths method. No fading of Feulgen dye in nuclei was found in 11 weeks, in contrast to considerable fading observed in earlier work when a different batch of basic fuchsin had been employed. Counts of radioactive nuclei in autoradiographs agreed well with microspectrophotometric results on the occurrance of DNA synthesis. In control cultures, with or without tritiated thymidine, DNA doubling took place in about 20% of the nuclei during the first two days but in few, if any, thereafter. It was confirmed that kinetin, as well as IAA, increases the frequency of nuclei undergoing DNA synthesis. However, IAA, in contrast with kinetin, still induced considerable DNA doubling after two days. Continued cell reproduction was maintained only in the presence of both substances. This work has been supported in part by research grants toK. Patau from the US Public Health Service (grant No. C-3313) and the American Cancer Society; and by grants toF. Skoog from the American Cancer Society and the Research Committee of the University of Wisconsin Graduate School with funds from the Wisconsin Alumni Research Foundation.     

Effect of malformin on the major constituents of Phaseolus vulgaris

Malformin inhibits wet and dry weight, nitrogen accumulation,and cell wall, RNA, DNA and protein synthesis in Phaseolus vulgaris.The relative proportion of dry matter and nitrogen in malformedtissues is increased in the ethanol soluble fraction and decreasedin the residue remaining after hydrolysis with 0.5 N HCl. Inhibitionof cell wall and protein synthesis was generally greater thaninhibition of nitrogen accumulation and RNA and DNA synthesis.The effects of malformin on the composition of P. vulgaris aresimilar to alterations in composition reported for ethylene,and opposite to those reported for gibberellic acid. ¹This research was supported by grant GB-7158 from the NationalScience Foundation and grant E-146-F from the American CancerSociety. ²Journal Paper No. 3509 of the Purdue Agricultural ExperimentStation. (Received October 23, 1968; )     

Intracellular development of a large DNA bacteriophage lytic for Caulobacter crescentus

Summary The cytological alterations accompanying Cb 13 infection of Caulobacter crescentus CB13 cells were followed by electron microscopic examination of sections of cells fixed at various stages of the infection. During the first half of the latent period, the cells appear unaltered. In the second half, the nucleoplasm migrates to the cell periphery and becomes more discrete than the nucleoplasm of uninfected cells. Phage particles appear within the migrated nucleoplasm. The only further alteration apparent in the sections is the absence of the lysozyme-versenesoluble layer of the cell wall of phage-lysed cells.This work was supported by National Science Foundation grant GB-2872.Dedicated to Professor C. B. van Niel on the occasion of his 70th birthday.     

Detection of anaerobic mycoplasmas in cell cultures

Summary A commercially available anaerobic generator and incubation system that develops a low oxidation-reduction potential was used for the assay of cell cultures for mycoplasmal contamination. Mycoplasma broth and agar media supplemented with dextrose, yeast extract, and horse serum were used. This system supported growth of some mycoplasmas that failed to grow in incubators with 5% CO₂ in nitrogen previously used in culture of mycoplasmas in this laboratory. This work was supported by a grant from the John A. Hartford Foundation General Research Support Grant No. 5 SO1 RR05582-4 from the National Institutes of Health, and by a Grant-in-Aid Contract from the State of New Jersey.     

Pattern recognition in several sequences: Consensus and alignment

The comparison of several sequences is central to many problems of molecular biology. Finding consensus patterns that define genetic control regions or that determine structural or functional themes are examples of these problems. Previously proposed methods, such as dynamic programming, are not adequate for solving problems of realistic size. This paper gives a new and practical solution for finding unknown patterns that occur imperfectly above a preset frequency. Algorithms for finding the patterns are given as well as estimates of statistical significance. This author supported by a grant from the System Development Foundation. This author supported by NSF grant MCS-8301960 and by a grant from the System Development Foundation. This author supported by NIH grant GM19036.     

Microtubule-kinetosome relationships in the motile cells of the Blastocladiales

Summary Motile cells of four members of the fungal order Blastocladiales have been examined with respect to distribution of intracellular microtubules. In all cases, the cellular microtubules originate from a sleeve of electron opaque material which surrounds the proximal third of the kinetosome. The microtubules run forward in the zoospores, ensheathing the nucleus and the nuclear cap before terminating at the anterior ends of the cells. Each cell contains 27 microtubules which are arranged in 9 groups of 3 tubules each. The significance of these observations with respect to centers of organization for microtubules is discussed.This work was supported by a grant (GB-4529) from the National Science Foundation.     

Three independent genetic systems that control initiation of a fungal fruiting body

Summary The initiation of monokaryotic fruiting in the basidiomycetous fungus Schizophyllum commune has been observed to occur spontaneously, in response to biochemical substances, and following mechanical injury. The responses to these three stimuli are genetically separable and under polygenic control.Paper #2259 from the Laboratory of Genetics, University of Wisconsin, Madison, Wisconsin 53706Supported in part by the College of Agriculture and Life Science, University of Wisconsin and NIH Predoctoral Training Grant #GM 07133 to the Laboratory of Genetics, University of WisconsinSupported in part by the College of Agriculture and Life Sciences, University of Wisconsin and by grant PCM77-05581 from the National Science Foundation     

Two water molds can grow without measurable turgor pressure

The water molds Achlya bisexualis Coker and Saprolegnia ferax (Gruithuisen) Thuret (Class: Oomycetes) normally grow in the form of slender hyphae with up to 0.8 MPa (8 bar) of internal pressure. Models of plant cell growth indicate that this turgor pressure drives the expansion of the cell wall. However, under conditions of prolonged osmotic stress, these species were able to grow in the absence of measurable turgor. Unpressurized cells of A. bisexualis grew in the form of a plasmodium-like colony on solid media, and produced a multinucleate yeast-like phase in liquid. By contrast, the morphology of S. ferax was unaffected by the loss of turgor, and the mold continued to generate tip-growing hyphae. Measurements of cell wall strength indicate that these microorganisms produce a very fluid wall in the region of surface growth, circumventing the usual requirement for turgor.Abbreviations DAPI 4,6-diamidino-2-phenylindole - PEG polyethylene glycol This work was supported by National Science Foundation grant DCB 90-17130.     

A cloned rat thymic epithelial cell line established from serum-free selective culture

Summary A serum-free system has been developed for selective growth and long-term culture of rat thymic epithelial cells. The growth media is a modification of McKeehan's WAJC 404, plus insulin, cholera toxin, dexamethasone, and epidermal growth factor. Cultures have been continuously passaged and maintained for over 6 mo., and a cloned cell line, TEA3A1, has been established. These cells are epithelial, judging by morphology and ultrastructure, and are positive for A2B5 and thymosin α markers for thymic endocrine cells. This work was partly supported by grant PCM-834 0582 from the National Science Foundation, Washington, DC, and grant P01 CA 37589-2 from the National Cancer Institute, Bethesda, MD.     

Inherent resistance of HeLa cell derivatives to paromomycin

Summary The human tumor-derived cell line HeLa S3 and nuclear and mitochondrial gene mutants derived from it are resistant to the aminoglycoside antibiotic, paromomycin (PAR). Other carcinoma-derived cells, SV40-transformed cells, and four human diploid fibroblast cell lines are all sensitive to PAR. Sensitivity is dependent on cell density, and at cell numbers greater than 400/cm² sensitive cells will proliferate in PAR. The resistance to PAR is inherited in a dominant manner in cell-to-cell fusion hybrids, but is not transferred in cytoplast-to-cell fusions. PAR resistance is therefore encoded by a nuclear gene(s). Resistance to PAR is not caused by changes in the response to mitochondrial or cytoplasmic protein synthesis to PAR in vitro. The uptake of PAR is similar in resistant and sensitive cells, and dimethyl sulfoxide does not render resistant cells more sensitive. Thus, HeLa cell PAR resistance is unlike previously reported ribosomal mutations and may derive from differences in the intracellular metabolism of PAR. This work was supported by National Institutes of Health grant number AG 02664, University of South Carolina Biomedical Research Support grant number S07 RR7160, and by a grant from the Elsa U. Pardee Foundation, all to C. L. B.     

A pancreatic polypeptide (PP)-like immunoreactant is present in the glicentin-containing cell of the cat intestine

Summary BPP-like immunoreactivity was identified in the intestinal mucosa of the cat. In light microscopy BPP immunoreactive cells were found identical to glicentin-containing cells or L-cells. By immunoelectronmicroscopy, BPP-like material was localized within the glicentin-containing secretory granules.This work was supported by grant nr. 3.120.77 from the Swiss National Science Foundation     

Passage number affects the pluripotency of mouse embryonic stem cells as judged by tetraploid embryo aggregation

The aim of this study was to determine whether the number of passages affected the developmental pluripotency of embryonic stem (ES) cells as measured by the attainment of adult fertile mice derived from embryonic stem (ES) cell/tetraploid embryo complementation. Thirty-six newborns were produced by the aggregation of tetraploid embryos and hybrid ES cells after various numbers of passages. These newborns were entirely derived from ES cells as judged by microsatellite DNA, coat-color phenotype, and germline transmission. Although 15 survived to adulthood, 17 died of respiratory failure, and four were eaten by their foster mother. From the 15 mice that reached adulthood and that could reproduce, none arose from ES cells at passage level 15 or more. All 15 arose from cells at passages 3–11. Our results demonstrate that the number of passages affects the developmental pluripotency of ES cells. This work was supported by the National Natural Science Foundation of China (grant no. 30571336) and the President Foundation of the Agricultural University of Hebei.     

Nutritional requirements of papiliomavirus-transformed mouse cells and an unifected parent line in serum-free culture

Summary A serum-free culture system was used to compare the nutritional requirements of mouse mammary cells transformed by bovine papillomavirus type 1 (ID13 cells) and the uninfected parent line (C127 cells). The serum-free, chemically defined medium used for this study was an MCDB 151-based medium (MCDB 151+S+I), supplemented with epidermal growth factor, transferrin, hydrocortisone, ethanolamine, phosphoethanolamine, retinoic acid, trace metals, and insulin. Proliferation of either cell type in serum-free culture required the addition of 250 μg/ml of insulin. ID13 cells have a doubling time of greater than 96 h in MCDB 151+S+I, whereas C127 cells have a doubling time of 60 h. This is in sharp contrast to the growth characteristics of the two cell types in 10% fetal bovine serum, where doubling times for the ID13 and C127 cells are 24 and 30 h, respectively. Culture of the cells in a serum-free medium has therefore revealed that the papillomavirus-transformed cells have more stringent growth requirements than the uninfected parent line. This work was supported in part by grant #1-P01 NS19214 from the National Institutes of Health, Bethesda, MD, NSF grant #R11-8217798 from the National Science Foundation, Washington, DC, and by a grant from the Otolaryngology Foundation.     

N-1-napthylphthalamic-acid-binding activity of a plasma membrane-rich fraction from maize coleoptiles

Summary Plasma membrane-rich fractions were prepared from maize coleoptiles by low-shear homogenization and differential and sucrose-gradient centrifugation. Plasma membrane fragments were identified using a specific cytochemical stain based on phosphotungstic acid prepared in chromic acid. In a comparison of 10 different cell fractions of varying plasma membrane content, the N-1-napthylphthalamic-acid (NPA)-binding activity of the fractions was directly proportional to the content of plasma membrane. The NPA binding appears to be strong K _M between 10^-8 and 10^-7 M) but non-covalent. NPA is known to inhibit auxin transport efficiently and quickly. Thus, the results are consistent with the localization of auxin transport sites at the plasma membrane of plant cells.Purdue University Agricultural Experiment Station Journal Paper No. 4355. This work was supported in part by a grant from the National Science Foundation GB-23183.Supported by National Science Foundation Postdoctoral Fellowship.