Effect of antioxidants, pro-oxidants, respiration inhibitors and substrates on the formation of autonomic secondary colonies of Fusarium bulbigenum var. blasticola

Autonomous secondary colonies are formed on the primary colonies of Fusarium bulbigenum var. blasticola grown in a synthetic Rieder medium. The secondary colonies are similar to genuine neoplasia in the following characteristics: dedifferentiation of the mycelium filamentous structure to yield single yeast-like cells, selective growth, faulty differentiation. Just as antioxidants and respiration substrates inhibit tumour formation and growth in higher organisms, they either prevent or inhibit the formation of secondary colonies in microorganisms. In contrast, their formation is stimulated when prooxidants and respiration inhibitors are added to the growth medium.     

Extracellular complementation of a developmental mutation implicates a small sporulation protein in aerial mycelium formation by S. coelicolor

The filamentous bacterium S. coelicolor differentiates by forming aerial hyphae, which protrude into the air and metamorphose into chains of spores. Aerial hyphae formation is associated with the production of a small, abundant protein, SapB, which is present in a zone around colonies of differentiating bacteria. Production of SapB is impaired in bld mutants, which are blocked in aerial hyphae formation, but not in whi mutants in which spore formation is prevented. We report that aerial hyphae formation by a newly identified bld mutant is restored by juxtaposition of the mutant near colonies of SapB-producing bacteria or by the application of the purified protein near mutant colonies. These observations implicate SapB in aerial mycelium formation and suggest that SapB is a morphogenetic protein that enables hyphae on the surface of colonies to grow into the air.     

COLONY FORMATION AND SEXUAL MORPHOGENESIS IN THE COCCOLITHOPHORE PLEUROCHRYSIS SP. (HAPTOPHYTA)1

Pleurochrysis sp. formed two types of symmetrical, diploid colonies on solid media: (i) single‐cell lineage (SCL) colonies and (ii) aggregation (AG) colonies. The first division of a single mother cell was asymmetric in ～54% of SCL colonies. These colonies developed at a slower rate than AG colonies. Diffusible molecules released from the cells acted like morphogens enhancing formation of AG colonies; their influence on chemotaxis of aggregating cells was dependent on concentration of the inoculum. Nitrogen depletion of diploid colonies induced sexual morphogenesis and colony patterning into inner and outer regions. The smaller innermost cells were surrounded by outer larger cells. Developmental mechanisms of colony formation were examined in relation to the heteromorphic, haplo‐diploid life cycle.     

Spatial organization of colonies of dimorphic micromycetes

The peculiarities of the formation of colonies of dimorphous epilithic fungus Phaeococcomyces de Hoog isolated from marble were studied. The data obtained can be used for modeling the formation of colonies of dimorphous microscopic fungi.     

Histological study of splenic colonies at different times following the transplantation of hematopoietic cells from embryonic liver

Histological analysis was carried out on the hemopoietic spleen colonies within 7 and 11 days after transplantation of the embryonic liver cells. Large superficial colonies were always present and were, predominantly, erythroid and mixed. Small superficial colonies consisted of undifferentiated cells and, unlike large colonies, appeared on the 11th day only. In the spleen thickness erythroid colonies predominated. The possibility of formation of small superficial 11 day colonies at the expense of pre-CFU-S is discussed.     

Ontogenetic changes in the capacity of the coral Pocillopora damicornis to originate branches

Most colonial corals vary intraspecifically in growth forms, and the diversity in branching morphology is especially striking. While the effects of environmental factors on growth forms have been studied, the genetic control of coral branching patterns has received little attention. The discovery of ontogenetic changes in the capacity to originate branching would set the stage for studies of how branch formation is genetically controlled. During experiments investigating contact reactions in the coral Pocillopora damicornis, we observed that young colonies derived from settled planulae and colonies regenerated from adult branch tips assumed different growth forms. Young colonies formed at least one branch from the central region of the colony, while colonies regenerated from adult branch tips (3-5 mm long) did not form branches during the 9-month observation period. This pattern was invariable, regardless of the types and outcomes of the contact experiments or the orientation of the branch tips. However, some fragments taken from 1- or 2-year-old colonies formed branches. This suggests that the rate of branch formation in P. damicornis colonies decreases with age. These findings will facilitate investigations of the mechanism of coral branch formation at the molecular level.     

Formation of bacterial colonies in successive time intervals

By enumerating colonies on a plate in successive equal short intervals of time, we found that the number of colonies formed in individual intervals varied at random and their distribution was approximated by a Poisson series. Based on the result, we derived the equation of colony formation (CF equation). This equation describes the relationship between the cumulative number of colonies and incubation time: N(t) = N infinity (1 - exp[-lambda(t - tr)]) where N(t) is the number of colonies at time t. N infinity, lambda, and tr are parameters, expressing the expected number of colonies on a plate at infinite incubation time, the probability of the occurrence of colony formation in a unit of time, and a retardation time, respectively.     

615小鼠ES细胞集落的分离及初步鉴定

目的　分离和培养 6 15小鼠的ES细胞集落 ,为建系打下基础。方法　以PMEF为饲养层分离 6 15小鼠的ES细胞集落 ,进行无饲养层培养 ,并对其进行初步鉴定。结果　ES细胞集落的出现率和传代成功率为 2 2 6 %和 0 94 % ,其ALP染色阳性 ,具有稳定的二倍体核型 ,可自发分化为多种类型的细胞。结论　成功分离和培养了6 15小鼠的ES细胞集落     

Murine B-cell stimulatory factor-1 (BSF-1)/interleukin-4 (IL-4) is a multilineage colony-stimulating factor that acts directly on primitive hemopoietic progenitors

Interleukin-4 (IL-4), which was originally identified as a B-cell growth factor, has been shown to produce diverse effects on hemopoietic progenitors. The present study investigated the effects of purified recombinant murine IL-4 on early hemopoetic progenitors in methylcellulose culture. IL-4 supported the formation of blast cell colonies and small granulocyte/macrophage (GM) colonies in cultures of marrow and spleen cells of normal mice as well as spleen cells of mice treated with 150 mg/kg 5-fluorouracil (5-FU) 4 days earlier. When the blast cell colonies were individually picked and replated in cultures containing WEHI-3 conditioned medium and erythropoietin (Ep), a variety of colonies were seen, including mixed erythroid colonies, indicating the multipotent nature of the blast cell colonies supported by IL-4. To test whether or not IL-4 affects multipotent progenitors directly, we replated pooled blast cells in cultures under varying conditions. In the presence of Ep, both IL-3 and IL-4 supported a similar number of granulocyte/erythrocyte/macrophage/megakaryocyte (GEMM) colonies. However, the number of GM colonies supported by IL-4 was significantly smaller than that supported by IL-3. When colony-supporting abilities of IL-4 and IL-3 were compared using day-4 post-5-FU spleen and day-2 post-5-FU marrow cells, IL-4 supported the formation of fewer blast cell colonies than did IL-3. IL-4 and IL-6 revealed synergy in support of colony formation from day 2 post-5-FU marrow cells. These results indicate that murine IL-4 is another direct-acting multilineage colony-stimulating factor (multi-CSF), similar to IL-3, that acts on primitive hemopoietic progenitors.     

Formation of bacterial colonies in successive time intervals.

By enumerating colonies on a plate in successive equal short intervals of time, we found that the number of colonies formed in individual intervals varied at random and their distribution was approximated by a Poisson series. Based on the result, we derived the equation of colony formation (CF equation). This equation describes the relationship between the cumulative number of colonies and incubation time: N(t) = N infinity (1 - exp[-lambda(t - tr)]) where N(t) is the number of colonies at time t. N infinity, lambda, and tr are parameters, expressing the expected number of colonies on a plate at infinite incubation time, the probability of the occurrence of colony formation in a unit of time, and a retardation time, respectively.     

Endogenous CFU-S in the djungarian hamster and the morphological typing of the colonies

The growth of macroscopic hemopoietic colonies was observed during postradiation regeneration in the spleen of dwarf hamsters (as well as of mice). The erythroid, granulocyte and megakaryocyte colonies were morphologically identified. The ratio between the erythroid and granulocyte colonies amounts to approximately 11. The formation of macroscopic spleen colonies and their morphology can be used for the functional characterization of hemopoietic microenvironment in the dwarf hamster.     

In vitro studies to prove the effect of sera of eosinophilia in colony formation

Serum samples from four patients with reactive eosinophilia and two patients with eosinophilic leukaemia were compared with normal sera with respect to formation of eosinophil colonies after addition of the sera to mononuclear cells from peripheral blood of healthy subjects. Supernatants from ConA stimulated guinea-pig spleen cells and human lymphocytes were tested in a similar way. Grown colonies were placed on glass slides and after staining with luxol fast blue the percentage of eosinophils was counted. The serum samples of the patients with reactive eosinophilia produced the greatest number of eosinophil colonies while supernatants of spleen and lymphocytes produced the greatest number of eosinophilic granulocytes. Our findings suggest the existence of a factor stimulating eosinophil colonies in the tested serum fractions. Beyond that an indication is given for a substance in the supernatants of spleen and lymphocyte suspensions which stimulates more intensively the maturing into eosinophilic granulocytes than the formation of colonies.     

The action of the cells of hemopoietic organs in chick embryos on mouse CFUdc and CLFUdc]

The humoral influence of cells of hemopoietic organs of chicken embryos of different terms on the development of the colony and cluster formation of mononuclears of the bone marrow of mice was studied in joint cultivation in two-compartment cylindrical diffuse microchambers. The process of formation of colonies and clusters is inhibited by cells of the yolk sac on the 2nd-4th day of the development, by cells of the liver on the 8th-12th day, of the spleen on the 13th-18th day and of the bone marrow--on the 15th day. The yolk sac cells were found to have most considerable inhibiting influence on proliferation and differentiation of cells on the 2nd day of the development of chicken embryo. The yolk sac cells on the 6th day stimulate the formation of colonies and clusters. The yolk sac, beginning from the 4th day of the development, and the liver release humoral factors promoting the formation of erythroid colonies. The erythroid colonies are formed but when cultivated on the vascular membrane of the chicken embryo; the erythroid colonies are not formed when cultivated in the abdominal cavity of mice. Local erythropoietinoid factors are not synthetized by the spleen and bone marrow cells. A supposition is put forward that a combination of the local inhibiting and erythropoietic effects promotes the erythroid differentiation of cells.     

A Confocal microscopic study on colony morphology and sporulation of Bacillus sp.

Hexavalent chromium Cr(VI) is one of the dominant oxidation states of chromium that exist in the environment and is highly toxic to all forms of life. In the present study, we employ a confocal laser scanning microscope (CLSM) and investigate the effect of Cr(VI) on colony morphology of a Bacillus sp. isolated from soil exposed to tannery effluent. The colonies grown at chromium concentrations, control and 100 ppm are found to be opaque and beyond 200 ppm the colonies were translucent thus exhibiting phase variation. CLSM studies on colonies grown on control plates showed significant increase in height and in biovolume as a function of time whereas, the translucent colonies showed very little change in height and biovolume corresponding to the colony growth. Exopolymeric substance (EPS) content of translucent colonies was lesser than that of opaque colonies, indicating that EPS also plays a role in the observed phenomenon of phase variation. Studies on the effect of Cr(VI) on spore formation showed that Cr(VI) concentrations up to 100 ppm favored spore formation, while concentrations beyond 100 ppm showed a steady decline in spore formation.     

Differentiation of Reproductive Cells in Volvox carteri*

SYNOPSIS. The life cycle of Volvox carteri was studied in axenic culture using the NB-3 and the NB-7 strains isolated from Nebraska. Vegetative colonies of both strains contain 8–12 asexual reproductive cells (gonidia) which divide to form daughter colonies. During daughter colony formation, the reproductive cells of the daughters are delimited at an early stage of cleavage. Gonidia are delimited at the division from 16 to 32 cells, but eggs and male initial cells are not differentiated until the division of the 32-celled stage. In all instances the reproductive cells are the products of unequal cleavages. Male and female colonies are formed in separate clones. Female colonies contain approximately 20 eggs. Male colonies have approximately 50 male initial cells, each of which forms a sperm bundle containing 64 or 128 sperm. Sperm bundles penetrate female colonies and fertilize the eggs. Zygote formation, zygote germination, and the development of gone colonies is described. Sexual type was inherited in a 1:1 ratio. Male colonies appear spontaneously in the male strain, but female colonies were formed in the female strain only in the presence of a substance produced by colonies from male cultures. This female inducing substance is produced in male cultures primarily, if not exclusively, by male colonies rather than by vegetative colonies. The female inducing substance is heat labile and non-dialyzable. Activity is destroyed by Pronase, but not by trypsin, chymotrypsin or ribonuclease. Gonidia appear to be most susceptible to female induction during the early stages of their expansion prior to cleavage.     

浮游动物诱发藻类群体的形成

从研究蓝藻水华形成机理的需要出发,综述了浮游动物的牧食压力对藻类群体形成的诱发作用。指出诱发藻类群体形成的化合物来自牧食性浮游动物对藻类的有效牧食,是藻类群体形成的重要原因之一,而这些诱发性的化合物并不是有关生物体的组成成分,是种间相互作用的结果。藻类群体的形成方式有源于一个母细胞的分裂和业已存在的单细胞的聚合两种方式,栅藻的诱发性群体可能是来自一个母细胞的分裂,而在其它藻类的诱发性群体形成如铜绿微囊藻则可能是业已存在的单细胞的聚合。由于藻类形成群体后能显著降低浮游动物对其牧食速率,因此,这种诱发性群体形成的现象,可以解释为藻类对变化的牧食压力的一种有效的反牧食防御策略,也是两者协同进化的结果。浮游动物对藻类群体形成的重要作用,在研究模拟蓝藻群体及水华形成值得借鉴应用。作者还提出推测,水华蓝藻的群体形成,可能就是在富营养化条件下藻类快速生长,加上浮游动物的牧食压力共同作用下联合驱动的结果,而这种群体形成很可能在积累到一定程度后,结合特定的气象水文等理化因子,就会聚集于水表“爆发”出肉眼可见的水华。因此,开展浮游动物牧食作用对水华蓝藻早期群体形成诱发效应的研究不仅能加深对水华形成的全面认识,而且对于进一步认识藻类的诱发性反牧食防御适应机制、揭示生态系统中生物之间的复杂关系也具有重要的理论意义。     

单种群菌落分形结构的形成及其机制研究

在变形杆菌、绿脓杆菌单种群菌落分形结构的形成过程中,细菌的运动、潜－生序变化及环境的营养水平是菌落形成扩散限制聚合模型（ＤＬＡ）分数维图样的关键。对菌落环境的分析结果显示单种群菌落中非平衡环境的形成是菌落分形结构产生的根本机制     

STUDIES OF HEMATOPOIESIS IN MURINE SPLEENS: SIGNIFICANCE OF HEMATOPOIETIC COLONIES FORMED ON THE SURFACE OF SPLEENS

Conies of hematopoietic tissue are formed in spleens of lethally irradiated mice by the injection of small numbers of hematopoietic cells. Some of these colonies appear as surface colonies, others can be identified only in serial sections of the spleen. The present studies have related the number and cellular composition of total hematopoietic colonies in the murine spleen to their visual recognition on the splenic surface. These studies demonstrate that only 50% of the total colonies in a spleen are recognized as surface colonies and that of those colonies on the surface, approximately 80% contain erythroid elements. At least four factors play important roles in the recognition of hematopoietic colonies as splenic surface colonies: (1) dose of repopulating cells or hematopoietic stem cells injected into the irradiated animal; (2) location of colonies within the spleen; (3) size of colonies; and (4) cellular content of the colonies. These studies demonstrate that surface colony formation reflects primarily erythropoiesis and not total hematopoiesis.     

Restriction of cloning potential in agarose of early chick embryonic cells as development progresses

Early chick embryonic cells, prior to the formation of the primitive streak, form colonies when cultured in soft agarose [Mitrani, E.: Exp. Cell Res. 152, 148-153 (1984)]. The present work is an attempt to determine at which stages of development this ability is expressed and which areas of the chick embryo harbour the colony-forming cells. We found that the capacity to form colonies decreases as development progresses and cells enter alternative differentiation pathways. At pre-primitive streak stages, the capacity is concentrated to the peripheral areas of the embryo and decreases towards the centre. With the onset of hypoblast formation only cells from Area Opaca and, to a lesser degree, the Marginal Zone, can form colonies in agarose. At post-primitive streak stages only extra-embryonic cells can form colonies in agarose. By 48 h of incubation all cells of the chick blastoderm seem to have lost the capacity to form colonies in agarose.     

Contacts between the cells in bacterial colonies

The interaction of cells in microbial colonies has been studied by electron-microscopic techniques. Two types of contacts between cells have been found to exist in the colonies of Gram-negative bacteria of the genera Escherichia, Shigella and Salmonella: close cell adhesion due to the fusion of cell-wall outer membranes and the formation of intersections consisting of membranous tubules. At the sites of close adhesion the fusion of cytoplasmic and outer membranes have been found to occur in Bayer's zones. In the colonies of Gram-positive bacteria of the genera Staphylococcus and Brevibacterium only one type of contacts has been revealed: the fusion of the peptidoglycan layers of the cell walls. The results of this study indicate that in colonies bacteria are not completely isolated; their interaction leads to the formation of a three-dimensional structure denoted as a cooperative cell system.