Quantitative immunogold ultracryomicrotome stidies of the distribution of periimplantation proteins in the sheep

Summary Several mammalian uterine and conceptus proteins are produced at specific stages of implantation. Ovine trophoblast protein-1 (OTP-1) is only synthesised of pregnancy (dpc). This immunogold ultracryosection study shows that, during this period, OTP-1 immunoreactivity is only found in the Golgi body of the trophectodermal cells. A second protein, of 14 kD molecular weight (14K protein), has a more varied distribution being found in membrane-bounded crystals in uterine epithelium and trophectodermal cells, and distributed throughout the cytosol and nucleoplasm of the uterine epithelium. There are only trace amounts of the 14 K protein in the fetomaternal syncytium which replaces the uterine epithelium during implantation, and no crystals are found in the trophectoderm after cotyledonary villus formation is initiated at 24–25 dpc. The crystals containing 14 K protein persist throughout pregnancy in the intercotyledonary areas. The narrow time window of OTP-1 occurrence reinforces the suggestion that this represents an important developmental signal, whereas the distribution of the 14 K protein indicates a more general nutritive function.     

Subcellular localization of thyrotropin-releasing hormone (TRH)- and Neuropeptide Y (NPY)-like immunoreactivity in the neurointermediate lobe of the frog pituitary

The presence of thyrotropin-releasing hormone (TRH) and neuropeptide Y (NPY) has been demonstrated in the neural lobe and in the intermediate lobe of the frog pituitary by immunocytochemistry on ultrathin sections of neurointermediate lobes obtained by cryoultramicrotomy. In the neural lobe, separate populations of TRH- or NPY-immunoreactive nerve fibers were observed. Both neuropeptides were contained in dense-core secretory vesicles about 200 nm in diameter. In intermediate lobe cells, TRH- and NPY-like immunoreactivities were observed in the cytoplasmic matrix and more sparsely in secretory granules. Occasionally, immunoreactive TRH could be visualized at the plasma membrane level. In the nucleus, both peptides were detected in the euchromatin, in the vicinity of the heterochromatin and in the nucleolus. Conversely, gonadotropin-releasing hormone-like immunoreactivity could not be detected. These results provide immunocytological evidence for the presence of endogenous TRH and NPY in frog melanotrophs indicating that these peptides may participate in the regulation of intermediate lobe secretion.     

Xiphinema index and Caenorhabditis elegans: preparation and molecular labeling of ultrathin frozen sections

A method for the orientation of nematodes for cryoultramicrotomy is described. Comparison of cryosections with sections prepared by conventional electron microscopic procedures showed satisfactory resolution of structural details in frozen sections. Labeling of frozen sections en face was achieved by cationized ferritin and colloidal iron. Actin was localized in cryosections of somatic muscle by immunoferritin labeling. The current study is a practical example of the application potential of cryoultramicrotomy to examination of nematode cytochemistry at a molecular level.     

Binding and internalization of native gonadoliberin (GnRH) by anterior pituitary gonadotrophs of the rat

Summary To identify anterior pituitary cell types containing GnRH binding sites and to study the internalization process of this peptide by target cells under physiological conditions, autoradiography was performed on rat anterior pituitaries removed at specific time intervals (2–60 min) after intravenous injection of mono-radioiodinated ¹²⁵I-GnRH into intact males. At electron-microscopic level, gonadotrophs and lactotrophs appeared to contain silver grains. Concomitant administration of an excess of unlabeled GnRH with the radioiodinated hormone prevented this localization indicating the specificity of the reaction. The time-course study in gonadotrophs showed that 2 min after injection silver grains could be found over the plasma membrane, secretory granules and nuclear membrane. Similar results were observed 5 and 15 min after injection. Extensive label was observed over the nucleus and nuclear membrane 15 to 60 min after injection. The injection of a radioiodinated GnRH agonist [D-Trp⁶, Pro⁹ (Net), DesGly¹⁰]-GnRH produced comparable results. In contrast, the injection of ¹²⁵I-[D-pGlu¹, D-Phe², Trp^3,6]-GnRH, an antagonist of GnRH, produced positive labeling only at the plasma membrane without internalization. These results indicate that, after binding with receptors on the plasma membrane, GnRH is rapidly internalized, accumulating in secretory granules, and localizing over the nuclear membrane and later, in the nucleus. Association of radioactivity with secretory granules could be related to a specific action of GnRH at this level or to receptor recycling, and presence of label in the nucleus may be related to stimulation of neosynthesis of LH and GnRH receptors.     

Cell wall architectures in a mycorrhizal association as revealed by cryoultramicrotomy

Summary In a vesicular-arbuscular mycorrhizal association a different texture in the cell wall of the host and fungus is revealed by using cryoultramicrotomy, that is a powerful tool in studying macromolecular arrangements. Using this technique the host wall displays fibrillar texture, whilst the fungal wall appears amorphous. The latter is not affected by the tested enzymatic digestions. On the contrary, it is labelled by ferritin linked to the wheat germ agglutinin, displaying the presence of N-acetylglucosamine. It is suggested that this sugar is present in single units or in short chains, whilst true chitin fibrils are not formed.     

Theileria parva: expression of a sporozoite surface coat antigen

A monoclonal antibody specific for the Theileria parva sporozoite, which recognizes a determinant on the surface coat and blocks sporozoite infectivity, was used to investigate the presence of the determinant on other stages of the parasite lifecycle. Immunofluorescence techniques did not demonstrate this determinant on the kinete, schizont, merozoite, or piroplasm stages of the parasite. Immunoautoradiography, using a tritiated form of the monoclonal antibody, on sections of infected salivary glands collected from ticks that had fed for 0, 1, 2, 3, or 4 days revealed that the determinant recognized was synthesized predominantly during sporogony, between 2 to 3 days after the tick started feeding. Immunoelectron microscopy was performed on ultrathin frozen sections of infected tick salivary glands incubated with the monoclonal antibody followed by Protein-A--colloidal gold. The antigen or its precursor could be detected in the developing parasite. In ticks fed 2 days, the sporoblast was labeled, both in the cytoplasm and on parasite membranes, often including the nuclear envelope. In sections from ticks fed 4 days, the sporozoite surface membrane was labeled, as were membrane-bounded sporozoite organelles identified as micronemes. Observation by immunofluorescence, on sporozoites incubated with bovine peripheral blood lymphocytes, suggested that the antigen recognized by the monoclonal antibody does not enter the lymphocyte during sporozoite endocytosis. We conclude that synthesis of the antigen or its precursor(s) occurs during sporogony in the feeding tick, at the time of maximal parasite proliferation, and precedes the formation of morphologically mature sporozoites; the antigen's role in the parasite life cycle also appears to be limited to events associated with the sporozoite entry process.     

Caenorhabditis elegans: Characters of negatively charged groups on the cuticle and intestine

Partial characterization of carboxyl, sulfate, and phosphate groups on the Caenorhabditis elegans cuticle and intestinal microvilli was achieved by en face labeling of floating cryosections at two pH levels and specific blockage of sulfate groups by Alcian blue. All negatively charged groups on the cuticle and intestinal microvilli labeled heavily at pH 7.2–7.4. Pretreatment to block sulfate groups followed by ferritin labeling at pH 7.2–7.4 gave a 35% reduction of binding on the cuticle and an 80% reduction in binding on the microvilli. At pH 1.8 or 2.5, only the sulfate groups labeled as shown by the complete abolition of labeling on the cuticle and the microvilli following blockage of the sulfate groups. Molecules with accessible sulfate groups were distributed in clusters throughout the cortical layer of the cuticle, were present in the struts of the median layer but were absent from the basal layer. The advantages of applying molecular probes to cryosections as compared to sections prepared by standard electron microscopical techniques are discussed.     

Schistosoma mansoni: development of the vitelline cell, its role in drug sequestration, and changes induced by Astiban.

The ultrastructure of four stages in the development of the vitelline cell of Schistosoma mansoni has been described, and the effect of different regimes of Astiban on the morphology of these cells was investigated. The drug had a highly selective action, rapidly destroying those cells at a stage of granular endoplasmic reticulum development, had a less immediate effect on the “mature” cells, and had no apparent effect on the first stages in development. These cells persisted and were able to continue development when the drug was withdrawn. Acid phosphatase tests at an ultrastructural level showed a considerable increase in activity in the cytosegresomes of affected “mature” cells. The ribosomal complexes present in the “mature” cells represent the early stages of cytosegresome formation, and these cytosegresomes increased in number in affected “mature” cells. X-ray analysis of both araldite and cryosections in the transmission electron microscope revealed a concentration of the element antimony in the cytosegresomes and vitelline droplets. On this basis, it is suggested that cytosegresomes play a role in drug sequestration by the vitelline cells.