Intracellular pH and the control of cell differentiation in Dictyostelium discoideum

Nature ◽  
1983 ◽  
Vol 303 (5914) ◽  
pp. 244-245 ◽  
Author(s):  
J. D. Gross ◽  
J. Bradbury ◽  
R. R. Kay ◽  
M. J. Peacey
Keyword(s):  
Cell Differentiation ◽  
Dictyostelium Discoideum ◽  
Intracellular Ph

Measurements of intracellular pH and its relevance to cell differentiation in Dictyostelium discoideum

1985 ◽  
Vol 76 (1) ◽  
pp. 235-245 ◽  
Author(s):  
K. Inouye
Keyword(s):  
Cell Differentiation ◽  
Dictyostelium Discoideum ◽  
Intracellular Ph ◽  
Spore Formation ◽  
Cell Contact ◽  
Weak Acids ◽  
Alternative Pathways ◽  
Monolayer Cultures ◽  
Fluorescence Dye ◽  
Good Accordance

A method was developed in this study to measure the intracellular pH (pHi) of Dictyostelium discoideum cells with a pH-sensitive fluorescence dye, carboxyfluorescein dibutyrate, and the pHi values of cells on the stalk and spore pathways were compared. The pHi of prestalk cells was lower than that of prespore cells by approximately 0.3 pH unit. In monolayer cultures of sporogenous mutants, which can differentiate into stalk cells and spores without cell contact, the pHi of the amoebae depended on the medium: media in which the majority of cells eventually become stalk cells reduced the pHi while conditions favouring spore formation increased the pHi. Addition of weak acids lowered the pHi. These results are in good accordance with the model presented by Gross and coworkers, which proposes that the choice between alternative pathways of cell differentiation is regulated via pHi and that low pHi favours stalk differentiation whereas high pHi favours spore formation.

scholarly journals Growth of myxamoebae of the cellular slime mould Dictyostelium discoideum in axenic culture

1970 ◽  
Vol 119 (2) ◽  
pp. 171-174 ◽  
Author(s):  
D. J. Watts ◽  
J. M. Ashworth
Keyword(s):  
Cell Differentiation ◽  
Dictyostelium Discoideum ◽  
Axenic Culture ◽  
Axenic Medium ◽  
Cellular Slime Mould ◽  
Slime Mould ◽  
Solid Media ◽  
Cellular Slime

1. A simple axenic medium suitable for the growth of the myxamoebae of a strain of the cellular slime mould Dictyostelium discoideum is described. 2. Procedures suitable for the growth of this strain in liquid and on solid media are described. 3. Conditions suitable for initiating the cell differentiation of myxamoebae grown axenically are described.

scholarly journals (Auto)Biographical reflections on the contributions of William F. Loomis (1940-2016) to Dictyostelium biology

2019 ◽  
Vol 63 (8-9-10) ◽  
pp. 343-357
Author(s):  
Adam Kuspa ◽  
Gad Shaulsky
Keyword(s):  
Cell Differentiation ◽  
Molecular Biology ◽  
Genetic Control ◽  
Dictyostelium Discoideum ◽  
University Of California ◽  
High Dimensional ◽  
Social Amoeba ◽  
The Social ◽  
The University ◽  
High Dimensional Datasets

William Farnsworth Loomis studied the social amoeba Dictyostelium discoideum for more than fifty years as a professor of biology at the University of California, San Diego, USA. This biographical reflection describes Dr. Loomis’ major scientific contributions to the field within a career arc that spanned the early days of molecular biology up to the present day where the acquisition of high-dimensional datasets drive research. Dr. Loomis explored the genetic control of social amoeba development, delineated mechanisms of cell differentiation, and significantly advanced genetic and genomic technology for the field. The details of Dr. Loomis’ multifaceted career are drawn from his published work, from an autobiographical essay that he wrote near the end of his career and from extensive conversations between him and the two authors, many of which took place on the deck of his beachfront home in Del Mar, California.

Differanisole A, an inducer of the differentiation of Friend leukemic cells, induces stalk cell differentiation in Dictyostelium discoideum

FEBS Letters ◽  
1993 ◽  
Vol 322 (1) ◽  
pp. 73-75 ◽  
Author(s):  
Yuzuru Kubohara ◽  
Koji Okamoto ◽  
Yoshimasa Tanaka ◽  
Ken-ichi Asahi ◽  
Akira Sakurai ◽  
...  
Keyword(s):  
Cell Differentiation ◽  
Dictyostelium Discoideum ◽  
Leukemic Cells ◽  
Stalk Cell

Nitric oxide, an endogenous regulator of Dictyostelium discoideum differentiation

Development ◽  
1997 ◽  
Vol 124 (18) ◽  
pp. 3587-3595
Author(s):  
Y.P. Tao ◽  
T.P. Misko ◽  
A.C. Howlett ◽  
C. Klein
Keyword(s):  
Nitric Oxide ◽  
Cell Differentiation ◽  
Dictyostelium Discoideum ◽  
Environmental Conditions ◽  
Initial Phase ◽  
Cell Aggregation ◽  
Developmental Cycle ◽  
Cell Signal ◽  
Constant Rate ◽  
Negative Effect

We have previously demonstrated that nitric oxide (NO)-generating compounds inhibit D. discoideum differentiation by preventing the initiation of cAMP pulses (Tao, Y., Howlett, A. and Klein, C. (1996) Cell. Signal. 8, 37–43). In the present study, we demonstrate that cells produce NO at a relatively constant rate during the initial phase of their developmental cycle. The addition of oxyhemoglobin, an NO scavenger, stimulates cell aggregation, suggesting that NO has a negative effect on the development of aggregation competence. Starvation of cells in the presence of glucose, which has been shown to prevent the initiation of cAMP pulses (Darmon, M. and Klein, C. (1978) Dev. Biol. 63, 377–389), results in an increased production of NO. The inhibition of cell aggregation by glucose treatment can be reversed by oxyhemoglobin. These findings indicate that NO is a signaling molecule for D. discoideum cells and that physiological or environmental conditions that enhance external NO levels will delay the initiation of cAMP pulses, which are essential for cell differentiation.

Ammonia depletion and DIF trigger stalk cell intact Dictyostelium discoideum slugs

Development ◽  
1989 ◽  
Vol 105 (3) ◽  
pp. 569-574 ◽  
Author(s):  
M. Wang ◽  
P. Schaap
Keyword(s):  
Cell Differentiation ◽  
Cyclic Amp ◽  
Dictyostelium Discoideum ◽  
Stalk Cell

The differentiation-inducing factor, DIF, was induce stalk cell differentiation in Dictyostelium incubated as submerged monolayers. We investigated the regulates the differentiation of stalk cells in the was found that in migrating or submerged slugs DIF cell differentiation, which is most likely due to the antagonist. Cyclic AMP and ammonia were earlier antagonists in vitro. We show here that ammonia, but an antagonist for DIF-induced stalk cell can induce stalk cell differentiation when ammonia are enzymically depleted. However, depletion of cAMP increase the efficacy of DIF. We propose that the cell differentiation during early culmination may be drop in ammonia levels inside the organism.

Zygote giant cell differentiation in Dictyostelium discoideum: biochemical markers of specific stages of sexual development

1992 ◽  
Vol 70 (10-11) ◽  
pp. 1200-1208 ◽  
Author(s):  
Darren D. Browning ◽  
Keith E. Lewis ◽  
Danton H. O'Day
Keyword(s):  
Alkaline Phosphatase ◽  
Cell Differentiation ◽  
Giant Cell ◽  
Dictyostelium Discoideum ◽  
Cell Fusion ◽  
Sexual Development ◽  
Giant Cells ◽  
Second Phase ◽  
Developmental Phase ◽  
Calcium Dependent

Sexual development in Dictyostelium discoideum has many unique features making it an attractive eukaryotic model system for the study of biomembrane fusion and intercellular communication. The work presented here provides primary biochemical evidence for two distinct phases during early sexual development that appear to be defined by calcium-dependent gamete cell fusion. In addition, we introduce a novel procedure for the enrichment of zygote giant cells and use this method to define certain wheat-germ agglutinin binding glycoproteins which are specifically located in zygote giant cells and others which are markers for surrounding amoebae in the second phase of development. In addition, a G protein which is present in high amounts early in development is unique to giant cells in the second phase, suggesting a role in phagocytosis. Finally, alkaline phosphatase activity was found to mark the first phase of sexual development, suggesting a role in cell fusion. This contrasts with the patterns of α-mannosidase and β-glucosidase activity that increase late in the second developmental phase, where they likely function in endocyte digestion during the cytophagic period. The developmental significance of these findings is discussed.Key words: zygote giant cell differentiation, Ca2+, glycoproteins, GTP-binding proteins, alkaline phosphatase, glycosidase, cell fusion.

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