Dictyostelium discoideum: Cell-type proportioning, cell-differentiation preference, cell fate, and the behavior of anterior-like cells in Hs1/Hs2 and G+/G− mixtures

Abstract. Conjugation in Tetrahymena is a cell interaction that involves the formation of pairs of cells of complementary mating types that are joined with opposite polarity at their anterior ends. Characteristically, it takes 1 h from the time cells are mixed until they begin to pair. We have previously shown that, during this time, the anterior tips of both mating types undergo morphogenetic transformation. The tips, which are normally pointed and ciliated, become truncated and cilia-free, and the cortical ridges disappear, leaving a smooth surface. We have also shown that the conjugation junction is formed during pairing by the apposition and alignment of two transformed surfaces. In the present study, we examined the binding of fluorescein-conjugated concanavalin A (F-Con A) in paraformalde-hyde-fixed cells at a stage when most cells have transformed tips but few are paired. We observed binding of Con A at anterior tips in a manner that was correlated with the extent of tip transformation. We further mapped the distribution of Con A receptors in conjugant pairs by orienting pairs with the plane of the junction perpendicular to the axis of illumination. It was observed that the distribution of Con A receptors formed a heart-shaped ring around the conjugation junction, in perfect accordance with the boundary line between the normal cortex and the transformed cortex. Additional experiments indicated that this binding pattern reflects the true distribution of receptors, suggesting that the receptors migrate from transformed tips to the junction ring in association with cell pairing. There is evidence that Con A receptors may have a function in cell adhesion in this system. Therefore, during this highly programmed cell interaction, the spatial redistribution of surface receptors and the morphological differentiation of the cell surface — both of wich may have a function in cell-cell attachment — are closely coordinated processes.     

Conjugation in Tetrahymena: the relationship between the division cycle and cell pairing

Conjugation, a sexual stage in the life cycle of Tetrahymena, is marked by the pairing of two cells of opposite mating types. Pairing establishes cytoplasmic continuity between the two cells and initiates the complex of nuclear events involved in sexual exchange. After mixing cells of opposite mating types in nonnutrient medium, a 3-hr refractory period ensues before pairing begins.A wave of cell division occurs concurrently with the onset of pairing. However, although all cells pair, the population does not double. This indicates that some cells do not divide and yet are capable of pairing. Apparently division per se is not required for pairing but does occur in most of the cells.Autoradiographic analysis demonstrates that the cells that divide before pairing were at a stage in the cell cycle beyond the initiation of macronuclear replication at the time they were transferred to nonnutrient medium. Cells that did not divide were in G₁ at the time of shift-down. Thus, neither replication nor division is required to be able to fuse. However, since fusion occurs only in G₁ and most cells are not in G₁ at the time of shift-down, a traverse of the cell cycle is required.Shift-down induces G₁ arrest and preparations for the mating reaction. Mixing the cells induces a synchronous wave of division for cells beyond the $\text{G}{}_1\text{S}$ interface. Preparations for the mating reaction occur independently of but simultaneous with the preparations for cell division.     

Cell surface interactions in conjugation: Tetrahymena ciliary membrane vesicles.

Tetrahymena ciliary membrane vesicles are shown to interact with preconjugant cells in a mating type-specific way. When cells are treated with vesicles of a different mating type before mixing for conjugation, cell pairing is enhanced, and the normal prepairing period is partially eliminated. This enhancement is mating type specific since it is not observed after pretreatment of cells with vesicles of their own mating type. In contrast, when vesicles are added at the time of mixing of two starved cultures, cell pairing is delayed in a concentration-dependent manner. By varying the conditions, we demonstrated enhancement or inhibition, or both. These results are interpreted in terms of two independent interactions of cells with vesicles. We suggest that first, vesicles substitute for another cell in cell-cell prepairing interaction and second, vesicles compete for adhesion sites produced during the prepairing period. Finally, the data presented are summarized within a speculative framework that calls attention to potential analogies with hormone-receptor signaling in mammalian cells.     

Conjugation in the Ciliate Euplotes octocarinatus: Comparison of Ciliary and Cell Body-Associated Glycoconjugates of Non-mating-Competent, Mating-Competent, and Conjugating Cells

Pair formation in the hypotrichous ciliate Euplotes octocarinatus is a poorly understood phenomenon. In order to obtain information about the molecules involved in this process, we compared ciliary and cell body-associated glycoconjugates of non-mating-competent, mating-competent, and conjugating cells. Detection of glycoconjugates was carried out on Western blots by immunostaining of oxidized, digoxigenin-labeled carbohydrate moieties. Using this method, in both of two complementary mating types a 130-kDa glycoprotein was identified, which appeared on cilia during acquisition of mating competence and was reduced during cell pairing. This suggests an active role of this glycoprotein in ciliary adhesion during pair formation, Additionally, in both of the two mating types a cell body-associated 135-kDa glycoprotein was detected, which is present in non-mating-competent cells as well as in mating-competent cells, but is strongly reduced in conjugating cells. In contrast to the ciliary 130-kDa glycoprotein, the cell body-associated 135-kDa glycoprotein is not surface-exposed [8]. We therefore propose that the cell body-associated glycoprotein is either involved in the preparation for cell fusion or meiosis or that it serves as a cytoplasmic pool for the ciliary 130-kDa glycoprotein.     

G1 arrest and the division/conjugation decision in Tetrahymena.

The transformation from the asexual proliferative stage of Tetrahymena to the sexual stage, during which cells of complementary mating types pair and nuclear fertilization occurs, provides an opportunity to study the relationship between the division cycle and differentiation. Conjugation is induced in cells starved for at least 2 hr by mixing complementary mating types. To determine the effect of starvation on the cell cycle, dividing cells were selected from a log growth culture and stepped down to non-nutrient conditions. The G₁ stage is operationally divisible into two sectors, A and B. In the A stage, cells arrest in nutrient-free medium. In the B stage, they proceed through the division cycle. Arrested G₁A cells may conjugate directly when challenged with similar cells of a complementary mating type. It is thereby demonstrated that Tetrahymena cells in G₁A can be directed to divide (nutrient conditions) or can be directed to differentiate (non-nutrient conditions plus complementary mating type) without an intervening division cycle. This rules out a requirement for reprogramming via chromosomal replication or cell division and suggests that G₁A is a stage during which the division/differentiation decision is made in direct response to ambient conditions.     

Conjugation Involving Dividing Cells of Tetrahymena thermophila

Feulgen-stained preparations of mixtures of starved Tetrahymena thermophila cells of complementary mating types have revealed an atypical form of conjugation involving cells which have completed the nuclear events of cell division, but have not undergone cytokinesis. Both micronuclei in the dividing cells are induced to undergo meiosis, but in 21 of 23 cases, the anterior micronucleus was activated 1st, suggesting that the meiotic inducer is synthesized near the mating junction and diffuses posteriad. Despite the induction of two micronuclei, “triad” conjugants appear to regulate nuclear events so as to produce a normal outcome.     

Conjugation involving dividing cells of Tetrahymena thermophila

Feulgen-stained preparations of mixtures of starved Tetrahymena thermophila cells of complementary mating types have revealed an atypical form of conjugation involving cells which have completed the nuclear events of cell division, but have not undergone cytokinesis. Both micronuclei in the dividing cells are induced to undergo meiosis, but in 21 of 23 cases, the anterior micronucleus was activated 1st, suggesting that the meiotic inducer is synthesized near the mating junction and diffuses posteriad. Despite the induction of two micronuclei, "triad" conjugants appear to regulate nuclear events so as to produce a normal outcome.     

Cell Pairing during Mating in Tetrahymena: I. Does Phagocytosis or a Cell Surface Receptor Participate in Con A Block?1

The lectin, Concanavalin A (Con A), inhibits cell pairing during mating in Tetrahymena and binds to the surface of pairing cells via receptors concentrated around the conjugation junction. Concanavalin A is also ingested in large amounts into food vacuoles. To dispel the possibility that Con A inhibits pairing via uptake into food vacuoles or through induction of food vacuole formation and to strengthen the idea that pairing is blocked through binding of Con A to cell surface receptors, we have conducted three types of experiments: 1) attempts to inhibit pairing by feeding with nutrients and with tantalum, a non-nutritive reagent; 2) a temporal analysis of the presence of food vacuoles in mating cells fed with tantalum; and 3) analysis of the restoration of pairing following the addition of α-methyl mannoside to cells previously treated with inhibitory concentrations of Con A. The results of these studies support the idea that Con A inhibits pairing by binding to receptors located on the cell surface and not by induction of or uptake into food vacuoles. We also present evidence that cells grown in an enriched proteose peptone medium are able to pair and undergo morphogenesis more readily than cells grown in 2% proteose peptone.     

Selective silencing of cell communication influences anteroposterior pattern formation in C. elegans

In C. elegans males, laterally located V cells generate a simple pattern of anterior alae (cuticular ridges) and posterior rays (mating sensilla). We have found that this pattern is generated, at least in part, by the selective interruption of cell-cell interactions. In anterior V cells, lineages leading to the production of alae are induced by cell interactions. These cell interactions are inhibited in specific posterior V cells by the activity of the gene pal-1, which allows these cells to generate rays instead of alae. The activities of cell signals and pal-1 appear to influence V cell fates by determining the state of a developmental switch that involves two homeotic genes, lin-22 and mab-5.     

Mating types in the ciliate Dileptus anser. Shortening of maturation period after micrurgical bisection of exconjugant cells

In many ciliates, young exconjugant clones demonstrate sexual immaturity: they are not able to conjugate with mature cells of complementary mating types (MTs). After several scores of cell divisions, a short period of adolescence (partial maturity) commonly occurs followed by maturation, after which these cells are able to conjugate with cells of other, i.e. complementary, MTs again. Tavrovskaja (1981) reported a significant reduction in the maturity period in Dileptus anser clones, grown from exconjugant ciliates regenerated from small cell fragments. To verify this, in the present study exconjugant D. anser cells were bisected with glass needle after 3 to 4 cell divisions following conjugation. The same procedure was performed with survived and regenerated cells on the 2nd and 3rd days. The clones thus obtained were cultivated, and their ability to mate with each of the three standard clones of MT I, II and III was tested week by week. Indeed, in 22 F1 clones from cross N 7C (MT I) x N 2 (MT II) the immaturity period was reduced 1.4-3.4-fold (2.18 in average) after a threefold bisection, as compared with that in intact subclones. Similarly, in 27 F1 clones from cross N 20 (MT I) x N 14 (MT II) this period was shortened 1.6-3.0-fold (2.19 in average). 12 of these clones showed a 0.9-2.4-fold (1.53 in average) reduction after a single bisection, and 1.6-2.8 (2.12 in average) after a threefold operation. Thus, micrurgical fragmentation of young exconjugant cells can be used to accelerate maturation in D. anser.     

Genetics of Chemical Induction of Conjugation in PARAMECIUM AURELIA

Certain stocks of P. aurelia, syngen 8, could not be induced to conjugate in a solution (KCl + acriflavine + calcium-poor conditions) which was effective in inducing conjugation in other species of Paramecium as well as in other stocks of syngen 8. Both stocks could conjugate by interaction with cells of complementary mating type. Breeding analysis shows that each of the two stocks is homozygous for a recessive gene that blocks induction of conjugation by the KCl-acriflavine solution. These two genes are neither allelic nor linked. Analyses of the phenotypes of the two uninducibles and the wild type were carried out by attempting to induce mating in cells of a single mating type by exposing them to detached mating-reactive cilia from cells of complementary mating type and to the KCl-acriflavine solution, either sequentially or simultaneously. The results confirm the conclusions of others that there is at least one unique step in chemical induction not shared with induction by interaction of complementary mating types. But the results also indicate that there is more than one unique step in chemical induction and that the effects of the two genes described here operate during different periods of the hour required for chemical induction.     

Costimulation in Tetrahymena. II. A nonspecific response to heterotypic cell--cell interactions

Costimulation, a developmental interaction requiring cell-to-cell contact, is the second stage in a linear sequence of events leading from vegetative growth to mating pairs in the ciliate Tetrahymena thermophila. This paper uses the kinetics of appearance of genetically marked progeny to measure accurately the duration of normal costimulation and then to examine the role of mating type in costimulation. Although diverse mating types are required for costimulation to occur, the costimulated cell's response is not specific to the mating type of the cell contacting it; costimulation by one mating type appears to prepare a cell for mating with any complementary mating type.     

"Fenestrin" and Conjugation in Tetrahymena thermophila

ABSTRACT Certain monoclonal antibodies interact with proteins of Tetrahymena thermophila found in the conjugation junction as well as around the gametic nuclei (pronuclei) of conjugating cells; they also react with the oral primordium and fission zone of vegetative cells and with the cytoproct and contractile vacuole pores of all cells. One of these (FXIX-3A7) was investigated in detail. Immunogold labelling suggests that the material labelled by the 3A7 monoclonal antibody, which we call “fenestrin,” is located beneath the epiplasm (membrane skeleton). Immunoblots reveal that the major and perhaps sole antigen is a 64 kDa polypeptide, found in two isoelectric variants. Developmental studies implicate fenestrin in two processes involved in conjugation. The first is “tip transformation.” During preliminary starvation (“initiation”), labelling of fenestrin first appeared as a spot at the anterior end of starved mature cells, then after mixing of different mating types (“costimulation”) it extended posteriorly along the anterior suture. After pairing, this region spread to form a widened plate. The second process is pronuclear transfer. Fenestrations representing channels between the conjugating cells began to appear 0.5 to 1 h after the conjugants united, and eventually merged to form a small number of temporary large holes during exchange of the transfer pronuclei. A fenestrin envelope also enclosed both the transfer and resident pronuclei; a strand of fenestrin connected the two. Shortly after pronuclear transfer, both transfer and resident pronuclei were released from fenestrin caps and fused to produce a zygotic nucleus (synkaryon) not associated with fenestrin. Fenestrin thus appears to be intimately involved in the process of pronuclear exchange.     

Mass selection of conditional mating mutants of Tetrahymena thermophila

The mating reaction in Tetrahymena thermophila includes a starvation period and two distinct cell interactions, co-stimulation and cell pairing, before the cells are cytoplasmically joined as conjugants. A selection procedure for harvesting mutants unable to mate at a restrictive temperature has been developed. A conjugant pair consisting of one cycloheximide-resistant cell and one wild-type cell (cycloheximide-sensitive) was itself sensitive to the drug. By adding cycloheximide and nutrient medium to a cross made at the restrictive and grow. Repetition of the selection procedure enriched for cells unable to conjugate at the restrictive temperature. The selected cells were able to grow at 38 degrees C and could conjugate at 28 degrees C. This procedure may be narrowed to select specifically for cell interaction mutants.     

Ontogenetic plate and plate field development in two chitons,Middendorffia andIschnochiton

Summary The larva ofIschnochiton gradually develops 6 transversal ridges and later a seventh one on its back. These intersegmental ridges are composed of two types of cells, one of them a goblet cell, as they are found in the girdle. Both types of cell seem to be responsible for cuticle secretion. The depressions between the ridges, called plate fields, are responsible for plate secretion. There are two different cell types. The marginal ones, which remain slender and tall, develop an enormous flat villus (here called a stragulum). Each plate field is tightly sealed against sea water by the stragulum. In the crystallization chamber formed by the stragulum, the first plate anlage is formed. In the later stages, the stragulum protects the growing plate margin. No periostracum is found. Most probably the cells developing the stragulum are responsible for the secretion of the tegmentum and in early development are the only secretory cells. The central cells of the plate field, which very soon flatten, then produce the second plate layer, the hypostracum. There is no secretion product in common to plate fields and intersegmental ridges. During the developmental period studied inIschnochiton (from hatching to 94 h) the number of cells of the individual plate field is not increased.The earliest anlage of the plates inMiddendorffia andIschnochiton is rodlike with straight margins and is not composed of several granules. Growth takes place at least inMiddendorffia by apposition of lime to the ends, posterior and, preferably, anterior margins. All plates are posttrochal.     

Mating types in Paramecium and a molecular approach to their determination

Mating types are expressed in ciliates for the duration of the mature period of their clonal cycle. During cell conjugation the reciprocal fertilization of complementary mating types takes place. Models of mating type determination in the Paramecium aurelia species complex based on classical genetics are reviewed including molecular aspects of the studies.     

Identification and characterization of a 38 kDa glycoprotein functionally associated with mating activity of Paramecium primaurelia

In Paramecium primaurelia mating interactions take place immediately after mixing mating-competent cells of opposite mating types. The cells clump in clusters (mating reaction) and then separate in pairs. Previous results have shown that sialic acid-containing glycoconjugates are present on the cell surface and are involved in mating-cell pairing. In order to identify the sialic acid-containing glycoprotein(s), we first metabolically radiolabelled non-mating-competent cells with D-[6-(3)H]galactose, and then analyzed the radiolabelled proteins by anion exchange chromatography. We characterized a 38 kDa (gp38) sialic acid-containing glycoprotein and raised the corresponding polyclonal antibody by means of which we localized the antigen at the level of the oral region of non-mating-competent cells and on the ciliary surface of mating-competent cells. Immunoblot analysis of the ciliary protein fraction showed that the anti-gp38 serum interacted with a 38 kDa protein in both mating types I and II cells. We also demonstrated the functional activity of gp38 in the mating reaction by means of anti-gp38 antibody competition assays.     

Sexual interaction ofEuplotes crassus: Differentiation of cellular surfaces in cell-to-cell union

A study by scanning electron microscope was performed to find out what cortical structures are differentiated by sexually interacting cells ofEuplotes crassus for their conjugant union. It was found that mixed cells of two complementary mating types, passed through an induction period, start uniting with each other by their ciliary membranelles which entwine around one another. Soon after, the two mating cells join more firmly by means of two linkages of the same type. Each linkage consists of the ciliary membranelles surrounding the left margin of the peristome of one pair's member to the ribbed wall limiting the right peristomial side of the partner. Remarkable changes in the architecture of the cellular cortex also occur after the initial interaction. In fact, an array of orderly longitudinal sequences of different kinds of protuberances is produced by just paired cells on their dorsal surface. In addition, membranelle cilia involved in the intercellular contact undergo discontinuous swelling along their length.     

A circadian rhythm of mating type reversals in Paramecium multimicronucleatum, syngen 2, and its genetic control

Two new alleles, C and c, involved in mating type expression were demonstrated. A dominant allele, C(cycler), must be present for the expression of the rhythm involving a sequential alternation of the two complementary mating types (III and IV). Cultures can be entrained with light-dark cycles. The phase of each clone can be characterized by its III to IV and IV to III transitions in relation to the zero hour of a given light-dark cycle. Phase is a stable phenotypic trait during asexual reproduction, but following sexual reproduction it does not display Mendelian segregation. Instead phase is determined through nuclear differentiation, i.e., the trait is controlled by differently determined macronuclear alagen (caryonidal inheritance) which normally segregate at the second cell division after conjugation. The phase of a clone within its genetic limits is a function of the photofractions and the light intensities used in the entraining treatment. By examining a number of clones a variety of phase angles between the mating type cycle and the entraining light-dark cycle are found. Dividing cells which are sexually unreactive and therefore do not express the rhythm can be entrained and following entrainment, phase is inherited through repeated cell replications at a rate greater than one fission a day in continuous darkness or continuous dim light. This result unique to this system indicates that the cellular processes underlying the phase and period of this circadian rhythm persist (unexpressed: sexual reactivity requires slight starvation) through repeated cell replications even when the division cycle is considerably shorter than the expressed circadian period. The rhythm has a circadian period in continuous darkness or light (tested for six days) of less than 24 hours. The reversal of mating type ceases in continuous light at higher intensities. Cells homozygous for the recessive allele, c(acyclic), do not reverse mating type but are either mating type III or IV, again as a consequence of nuclear differentiation. Since individual cells with the dominant allele express both mating types, differentiation for mating type can not involve the absence in the macronucleus of mating type determining factors.