Ultrastructure of spermiogenesis in the American alligator,Alligator mississippiensis (Reptilia,Crocodylia, Alligatoridae)

Testicular samples were collected to describe the ultrastructure of spermiogenisis in Alligator mississipiensis (American Alligator). Spermiogenesis commences with an acrosome vesicle forming from Golgi transport vesicles. An acrosome granule forms during vesicle contact with the nucleus, and remains posterior until mid to late elongation when it diffuses uniformly throughout the acrosomal lumen. The nucleus has uniform diffuse chromatin with small indices of heterochromatin, and the condensation of DNA is granular. The subacrosome space develops early, enlarges during elongation, and accumulates a thick layer of dark staining granules. Once the acrosome has completed its development, the nucleus of the early elongating spermatid becomes associated with the cell membrane flattening the acrosome vesicle on the apical surface of the nucleus, which aids in the migration of the acrosomal shoulders laterally. One endonuclear canal is present where the perforatorium resides. A prominent longitudinal manchette is associated with the nuclei of late elongating spermatids, and less numerous circular microtubules are observed close to the acrosome complex. The microtubule doublets of the midpiece axoneme are surrounded by a layer of dense staining granular material. The mitochondria of the midpiece abut the proximal centriole resulting in a very short neck region, and possess tubular cristae internally and concentric layers of cristae superficially. A fibrous sheath surrounds only the axoneme of the principal piece. Characters not previously described during spermiogenesis in any other amniote are observed and include (1) an endoplasmic reticulum cap during early acrosome development, (2) a concentric ring of endoplasmic reticulum around the nucleus of early to middle elongating spermatids, (3) a band of endoplasmic reticulum around the acrosome complex of late developing elongate spermatids, and (4) midpiece mitochondria that have both tubular and concentric layers of cristae. J. Morphol., 2010. © 2010 Wiley‐Liss, Inc.     

MEMBRANOUS STRUCTURES IN YEASTS

1. Most yeast cells carrying out active respiration have spherical or ellipsoidal mitochondria, with plate-like cristae. 2. Cytoplasmic petite strains of Saccharomyces cerevisiae have aberrant mitochondria, often containing whorled membranes. Mutants with deficiencies in the tricarboxylic acid cycle have mitochondria which appear normal when the cells are grown in low levels of glucose. 3. Cells of normal and petite S. cerevisiae grown strictly anaerobically show no recognizable mitochondrial profiles. 4. Carbon substrates which can only be respired promote the development of well-defined mitochondria. In certain facultatively anaerobic yeasts respiration is suppressed by glucose and the mitochondria under these conditions are large, pleomorphic and few in number. Other fermentable carbohydrates do not give this repression. 5. A number of antibacterial antibiotics, which inhibit mitochondrial protein synthesis, cause a disorganization of the mitochondrial cristae. 6. In yeast cells adapting from anaerobic to aerobic conditions mitochondria appear to develop from proliferations of the endoplasmic reticulum, which become progressively more organized. 7. Vacuoles often contain granular material, but in S. cerevisiae the vacuole, which has been described as a lysosome, frequently contains myelin-like lipid inclusions. The material in these inclusions is apparently derived from spherosomes. 8. Endoplasmic reticulum, orientated parallel to the plasmalemma, may be associated with fermentative ability in certain facultatively anaerobic yeasts. Endoplasmic reticulum is also actively involved in the budding process. 9. Normally the yeast-cell plasmalemma shows only minor convolutions, but in chloramphenicol-grown Rhodotorula glutinis the plasmalemma produces vesicular structures termed ‘paramural bodies’. 10. The yeast nuclear membrane has about 200 pores occupying 6–8 % of the total surface area. The nuclear membrane remains intact during mitotic division in yeasts until the daughter nuclei separate.     

Pre-fertilization degeneration of both synergids in Brassica campestris ovules

Summary In Brassica campestris, both synergids of the ovule degenerate before the arrival of the pollen tube. Synergid degeneration does not depend on pollination. At the non-degenerated stage, the synergids are completely filled with a complexly organized cytoplasm containing numerous mitochondria with many cristae, a large number of dictyosomes with many associated vesicles, and a very extensive rough endoplasmic reticulum. The degenerative changes that occur in the cytoplasm of the synergids are characterized by a loss of visibility of the membranes of the endoplasmic reticulum and the simultaneous formation of dense deposits on the surrounding membranes of the mitochondria. Locally, the plasma membranes of the synergids disappear, and some ground plasma of the synergids penetrates into the space between the plasma membranes of the egg cell and the central cell.     

Structure of Mitochondria and Activity of Their Respiratory Chain in Successive Generations of Yeast Cells Exposed to He-Ne Laser Light

The data on the aftereffect of He-Ne laser light (λ = 632.8 nm) on mitochondria of yeasts in late log phase were reviewed. The quantitative analysis of the ultrathin cell sections demonstrated a nonuniform thickness of the giant branched mitochondria typical for budding yeasts. Exposure to a dose of 460 J/m² (accelerating cell proliferation and activating respiratory chain enzymes, cytochrome c oxidase and NADH dehydrogenase), changed the macrostructure of the giant mitochondria—much of the narrow regions of the mitochondrial tube with profiles ≤0.06 μm² were expanded (while no signs of organelle damage were observed). Such mitochondria are characterized by increased relative surface area of the cristae, which can be due to the activation of their respiration and ATP synthesis. The number of associations between mitochondria and endoplasmic reticulum increased in irradiated cells in early log phase, which reflects the increased capacity of mitochondria to uptake Ca²⁺. Altered giant mitochondria configuration can increase the efficiency of both energy transfer and Ca²⁺ propagation through the cytoplasm. __________ Translated from Izvestiya Akademii Nauk, Seriya Biologicheskaya, No. 6, 2005, pp. 672–683. Original Russian Text Copyright ? 2005 by Manteifel, Karu.     

Seasonal Ultrastructural Changes of Leydig Cells in Lacerta muralis

We have studied the ultrastructure of the testis and interstitial tissue of lizard Lacerta muralis sacrificed in spring, summer and autumn, with special emphasis on the morphological changes of Leydig cells. From the autumn to the end of spring, Leydig cells showed a large smooth endoplasmic reticulum and mitochondria with tubular cristae. These features correlate with the synthesis and secretion of androgens. At the end of spring and after mating, the amount of smooth endoplasmic reticulum decreased and the mitochondria showed laminar cristae. Both features are typical of a latent period, during which time secretion of androgens remains inactive until the end of summer. The possible role of other cell organelles, such as Golgi complex and lysosome-like electron dense bodies, during both secreting and resting periods, is also discussed. Finally, we consider the relationship between seasons, secretory activity of Leydig cells and the spermatogenic cycle.     

Studies of the functional activity of mitochondria and cell ultrastructure of the coleoptile in wheat,Agropyron and their hybrids (incomplete amphidiploids) during decreasing temperature

Summary The structure of the mitochondria and endoplasmic reticulum in the coleoptile of plants (Triticum aestivum var. Lutescens 329, Agropyron glaucum, Triticum × Agropyron 56-chromosome hybrids, incomplete amphidiploids, TAH, containing 42 wheat chromosomes and 14 chromosomes of genomes D or X of Agropyron), which differ in winterhardiness, was studied after exposure to 0 ° and -4 °C for periods varying from 10 min to 4 days. The functional activity of mitochondria isolated from 3 day old seedlings was also investigated in these cereals. The cells of Triticum and Agropyron seedlings grown at 23 °C were shown to differ in mitochondrial structure. In the cells of TAH both kinds of mitochondria were found.On day 4 of exposure to -4 °C, the mitochondria of Agropyron cells were not changed; the endoplasmic reticulum formed complex closed cavities. Under similar conditions most wheat mitochondria were destroyed and in the rest no cristae were observed.Morphometric analysis indicated that the volume of such mitochondria increases by two times, while the surface area of the internal membranes and cristae decreases by 1.54 times. In such cells, the endoplasmic reticulum is represented only by membranes of the smooth type. The structure of the mitochondria and endoplasmic reticulum in the seedling cells of TAH 829, which is more like Agropyron in winterhardiness, is similar to that of Agropyron cells; in hybrid 822 (more like wheat containing the D genome), changes arise resembling those observed in wheat. The existence of different types of mitochondria in seedling cells of TAH is especially distinct at low temperatures.The mitochondria of the cereals studied differ in biochemical activity after low temperature treatment (0 ° and — 4 °C). Phosphorylative and oxidative activity of mitochondria of the winterhardy forms (Agropyron glaucum, TAH 829) decreases just after the beginning of low temperature treatment. At the same time, the morphology of the mitochondria undergoes reversible changes. The mitochondria of cold-susceptible forms of wintering plants (Triticum aestivum, TAH 822) do not conform to this pattern. Under long-term low temperature treatment they display irreversibly damaged mitochondria. It is suggested that the winterhardy forms have high adaptability connected with a rapid protective response of the cell mitochondria and endoplasmic reticulum. This adaptability is regulated by nuclear genes: TAH have different mitochondria in the coleoptile cells; if genome X of Agropyron is present, which TAH derives from the male parent, the related mitochondria become more resistant to low temperature treatment.     

Ultrastructural comparison of incompatible and compatible interactions in the barley powdery mildew disease

Summary In the powdery mildew disease of barley,Erysiphe graminis f. sp.hordei forms an intimate relationship with compatible hosts, in which haustoria form in epidermal cells with no obvious detrimental effects on the host until late in the infection sequence. In incompatible interactions, by contrast, the deposition of papillae and localized host cell death have been correlated with the cessation of growth byE. g. hordei. With the advent of improved, low temperature methods of sample preparation, we felt that it was useful to reevaluate the structural details of interactions between barley andE. g. hordei by transmission electron microscopy. The haustoria that develop in susceptible barley lines appear highly metabolically active based on the occurrrence of abundant endoplasmic reticulum, Golgi-like cisternae, and vesicles. In comparison, haustoria found in the resistant barley line exhibited varying signs of degradation. A striking clearing of the matrix and loss of cristae were typical early changes in the haustorial mitochondria in incompatible interactions. The absence of distinct endoplasmic reticulum and Golgi-like cisternae, the formation of vacuoles, and the occurrence of a distended sheath were characteristic of intermediate stages of haustorial degeneration. At more advanced stages of degeneration, haustoria were dominated by large vacuoles containing membrane fragments. This process of degeneration was not observed in haustoria ofE. g. hordei developing in the susceptible barley line.Abbreviations b endoplasmic reticulum extension, blebbing - er endoplasmic reticulum - f fibrillar material - g Golgi-like structure - h haustorium - hb haustorial body - hcw haustorial cell wall - hcy haustorial cytoplasm - hf haustorial finger - hocw host cell wall - hocy host cytoplasm - 1 lipid-like droplet - m mitochondrion - mt microtubule - mve multivesicular body - n nucleus - p papilla - ph penetration site of an infection peg - pl plasma membrane - s sheath - sm extrahaustorial membrane - v vacuole - ve vesicle     

Influence of the cytoskeleton,energy supply,and protein synthesis on the structure of the endoplasmic reticulum

Summary FITC-Con A fluorescence was used to visualize rER arrangement of endothelial cells derived fromXenopus laevis tadpole hearts. In particular determinants of rER organization, intracellular localization and the interrelationships with other organelles were analysed. rER occurs in association with nucleus, mitochondria and microtubules.The structure of rER is strongly affected by energy metabolism and by microtubules. In order to elucidate the interdependence of structure and function we examined the influence of cellular respiration, net lactate production and protein synthesis on rER morphology, as well as the relationship between energy metabolism and protein synthesis. ER morphology is determined primarily by energy consuming intracellular transport mechanisms. Energy needed for protein synthesis is supplied by the respiratory chain while ATP from aerobic glycolysis only compensates when respiration is disturbed.Abbreviations ACM amphibian culture medium - ATP adenosine triphosphate - FITC-Con A fluoresceine-isothiocyanate-coupled con-canavalin A - MT microtubule - rER rough endoplasmic reticulum - sER smooth endoplasmic reticulum - TRITC-phalloidin tetramethyl-rhodaminyl-isothiocyanate-coupled phalloidin - pXTH primary cells fromXenopus laevis tadpole hearts - XTH-2 endothelial cell line derived fromXenopus laevis tadpole hearts     

Ultrastructural studies of differentiation in the oocyte of the polyclad turbellarian,Prostheceraeus floridanus

Oocyte differentiation in the polyclad turbellarian Prostheceraeus floridanus has been examined to determine the nature of oogenesis in a primitive spiralian. The process has been divided into five stages. (1) The early oocyte: This stage is characterized by a large germinal vesicle surrounded by dense granular material associated with the nuclear pores and with mitochondria. (2) The vesicle stage: The endoplasmic reticulum is organized into sheets which often contain dense particles. Vesicles are found in clusters in the cytoplasm, some of which are revealed to be lysosomes by treatment with the Gomori acid phosphatase medium. (3) Cortical granule formation: Cortical granules are formed by the fusion of filled Golgi vasuoles which have been released from the Golgi saccules. The association between the endoplasmic reticulum and Golgi suggests that protein is synthesized in the ER and transferred to the Golgi where polysaccharides are added to form nascent cortical granules. (4) Yolk synthesis: After a large number of cortical granules are synthesized, yolk bodies appear. They originate as small membrane-bound vesicles containing flocculent material which subsequently increase in size and become more compact. Connections between the forming yolk bodies and the endoplasmic reticulum indicate that yolk synthesis occurs in the ER. (5) Mature egg: In the final stage, the cortical granules move to the periphery and yolk platelets and glycogen fill the egg. At no time is there any evidence of uptake of macromolecules at the oocyte surface. Except for occasional desmosomes between early oocytes, no membrane specialization or cell associations are seen throughout oogenesis. Each oocyte develops as an independent entity, a conclusion supported by the lack of an organized ovary.     

Oösorption in the Coleopteran Sitophilus granorius (L.)

King, P. E., Al-Khalifa, M. S. 1980. Oösorption in the coleopteran Sitophilus granarius (L.). (Department of Zoology, University College, Swansea, U.K.) — Acta zool. (Stockh.) 61(2): 79–86. The process of oösorption in the terminal oöcytes of starved specimens of Sitophilus granarius is described Starvation affects the nucleus, mitochondria and endoplasmic reticulum in both the follicle cells and the oöcyte. Glycogen disappears from the oöcyte at an early stage and islands are formed in the oö:cyte by infoldings of the combined follicle, oöcyte cell membranes.     

The Oxidative Phosphorylation and ATPase Activity of Arum spadix Mitochondria in Relation to Heat Generation

The respiration of Arum spadix mitochondria is coupled to asub-maximal stoichiometry of ATP synthesis. The P/O ratios associatedwith the oxidation of succinate or malate are decreased by antimycinand increased by m-chlorobenzhydroxamic acid, an inhibitor ofthe alternative oxidase. The mitochondrial ATPase activity of20–40 nmol (mg protein)^–1 min^–1 is independentof the maturity of the spadix and is unlikely to provide themechanism for heat production during the odoriferous stage,which probably results from an increase in the rate of electrontransport via the non-phosphorylating, cyanide-insensitive oxidase.     

Ultrastructural Characteristics of Adult Rat Adrenocortical Cells Maintained in vitro With and Without ACTH

Bhattacharyya, T. K., Butler, D. G., Price, C. S. 1980. Ultrastructural characteristics of adult rat adrenocortical cells maintained in vitro with and without ACTH. (Ramsay Wright Zoological Laboratories, Department of Zoology, University of Toronto, and Division of Endocrinology, Toronto Western Hospital, and Department of Medicine, University of Toronto, Canada.) — Acta zool. (Stockh.) 61(1): 9–21. The ultrastructural morphology of adrenocortical cells of adult rats maintained in culture for four days with and without corticotropin (ACTH) was studied in comparison to freshly dissociated cells. Identification of cells belonging to zona glomerulosa, zona fasciculata, and zona reticularis was made on the characteristics of the mitochondria and smooth endoplasmic reticulum (SER), and was confirmed by comparison with cellular layers from intact adrenals. Without ACTH, glomerulosa and fasciculata cells showed disappearance of SER, atrophied Golgi apparatus (GA), and a striking proliferation of granular reticulum. Fascicular cells had a loss in mitochondrial matrix density and the mitochondrial cristae showed a tendency to convert to lamellar glomerulosa-type cristae. Zona reticularis cells were not strikingly altered. Maintenance with ACTH led to increased cell size and islet formation of cortical cells. Glomerulosa cells had normal appearance and fasciculata cells manifested a pronounced development of GA and SER, and a normal configuration of mitochondria. The effects of ACTH on glomerulosa cells suggest a trophic influence of ACTH on these cells in vitro. The alterations observed in fascicular cell mitochondria and SER can be explained in terms of known concepts of steroid biosynthesis and basically agree with the patterns of steroid synthesis observed in these cells previously (Price et al. 1975).     

The cell structure of the reticulopodial amoeba <Emphasis Type="Italic">Filoreta marina</Emphasis> Bass et Cavalier-Smith (Cercozoa)

The cell structure of a reticulopodial amoeba, Filoreta marina Bass et Cavalier-Smith, is described. The cell is covered by a unitary membrane; glycostyles are absent. The life cycle comprises the uninucleate stage, multinucleate plasmodium, and spherical uninucleate cysts. The microtubules inside pseudopodia and the flagella are absent. The vesicular nuclei, endoplasmic reticulum, and Golgi apparatus are of a typical structure. The plasmodium produces a branched network of narrow anastomosing (reticulopodia) and wide pseudopodia. Thin unbranched micropseudopodia have also been observed. Oval mitochondria with a size of 0.3 × 0.6 μm contain the tubular cristae. A bidirectional motion of the cytoplasm inside the reticulopodia has been detected. Extrusomes (extrusive organelles) have not been found. The contractile vacuole is absent. F. marina feeds on bacteria. A similarity of this amoeba to other filose and reticulopodial amoebas is discussed.     

ULTRASTRUCTURAL CHANGES IN HAPLOID EMBRYOIDS OF LARIX DECIDUA DURING EARLY EMBRYOGENESIS

Cultures of haploid tissue derived from megagametophyte tissue were investigated at various stages of embryoid development. At the earliest stage of development the cells were vacuolate and plastids and mitochondria were simple in structure. Eventually, embryonal domes were formed which in turn, produced suspensor cells. As the embryoid developed, its apical cells showed increased complexity of plastids, eventually developing chloroplasts and amyloplasts. In addition, the vacuolar volume in the cells was reduced, while vesicle production increased. Cristae in mitochondria became more apparent. In the suspensor cells, plastids remained as leucoplasts and amyloplasts without any internal membrane structures. Mitochondria became more developed and vesicle number increased in the long cells. Smooth endoplasmic reticulum, which was the most common form of this class of membrane, was reduced by the cotyledonary stage and replaced by rough endoplasmic reticulum. Phenolic deposits appeared with maturation of the suspensor, and an extracellular matrix of PATAg (Thiery) positive polysaccharide was detected between the cells.     

The reversibility of the ethidium bromide-induced alterations of mitochondrial structure and function in the cellular slime mold,Dictyostelium discoideum

Addition of ethidium bromide to ameboid cultures of the slime mold,Dictyostelium discoideum, caused a cessation of cell division after 1 or 2 generations. The replication of mitochondrial DNA was immediately blocked as indicated by the 50% decrease in the DNA content of purified mitochondria from ethidium-bromide-treated cultures. The activity of the respiratory chain was also inhibited, resulting in a 75% decrease in cyanide-sensitive whole cell respiration. Spectral analysis at low temperature indicated that the amount of cytochromec ₁ was decreased 80% and that of cytochromec increased 100% in mitochondria from treated cells. Two cytochromesb absorbing at 556 and 561 nm were observed in mitochondria from both control and ethidium-bromide-treated cultures. The content of cytochromeb ₅₆₁ appeared to decline more than didb ₅₅₆, but it is hard to quantitate the decrease. The effects of ethidium bromide were fully reversible. When the drug was removed, the cells resumed a normal growth rate without any discernible lag. The activity of oligomycin-sensitive ATPase, cytochrome oxidase, and succinate-cytochrome-c reductase as well as the cytochrome content began to increase after 1 day returning to control levels within 5 days. Electron micrographs of whole cells treated with ethidium bromide revealed that mitochondrial profiles were elongated and had greatly reduced cristae. Numerous membrane whorls were apparent, as was a profound loss of rough endoplasmic reticulum. Three days after removal of ethidium bromide, mitochondria were again ovoid in shape and contained well-developed cristae. In all of the cells during recovery, there was a single large vacuole that appeared to enclose a large portion of the cell volume, forming a new cellular compartment that may simplify the breakdown of previously damaged organelles.This work is in partial fulfillment of the requirements for the Doctor of Philosophy degree at the City University of New York.     

Cytological features of developing embryogenic callus and somatic embryos of Iris pumila L. and Iris setosa Pall

Abstract

Cytological examination during somatic embryogenesis in Iris pumila L. and Iris setosa Pall, were performed using light and electron microscopy. The first sign of the cellular differentiation in the initial embryogenic callus (EC; stage 1) of both Iris species was the formation of short and elongated cell types. After the onset of embryogenesis, short cells divided producing a mass of densely packed meristematic cells, closely connected with numerous plasmodesmata. Further differentiation into globular embryos (GE) led to a loss of plasmodesmata and cell separation. In vacuolated elongated cells, cytoplasm was located near the wall and around the nucleus. In both cell types amyloplasts and small mitochondria with poorly developed crystae were abundant.

Cell of GE (stage 2) contained an increased number of mitochondria and plastids comparing to those from stage 1, indicating further differentiation. Thylakoids and starch grains were observed within the plastids, while the number of cristae within the mitochondria was increasing.

In cells of embryos with coleoptile (ECl) (stage 3), plastids differentiated into chloroplasts with thylakoids. In all stages of cell differentiation, short and long cisternae of endoplasmic reticulum with ribosomes were seen. Activity of dictyosomes was increased in stages 1 and 2, then reduced in stage 3.

Ultrastructure of EC cells was identical to that of proembryogenic cells, i.e. of early GE. Ultrastructural appearance of GE cells was identical in both Iris species, but evident, and increasing, differences in mitochondria and plastids were observed between GE and ECl embryos.The presence of bi-, three- and eight- cell proembryos demonstrates that they originate from a single cell in both Iris species.     

Ultrastructure of spermatogenesis in Cerastoderma glaucum (Cardiacea) and Spisula subtruncata (Mactracea)

Summary

In Cerastoderma glaucum, Sertoli cells are rich in lipids, glycogen and lysosomes, and premeiotic cells exhibited nuage, a prominent Golgi complex and endoplasmic reticulum cisternae encircling the nucleus. The Golgi complex gives rise to proacrosomal vesicles during mid-spermiogenesis, and the round acrosomal vesicle, with a dense fibrillar core, migrates laterally while linked to the plasma membrane as it develops the subacrosomal material. In its final position, the vesicle becomes cap-shaped (0.6 μm) and differentiates into apical light and basal dense regions. The elongated and helicoidal nucleus (8–9.9 μm) has a thin tip (0.3 μm) that invades the subacrosomal space, and in the midpiece (0.8 μm) two of the four mitochondria extend laterally to the nucleus (1.5–2.1 μm). In Spisula subtruncata, Sertoli cells are rich in lipids, glycogen and phagocytosed sperm. Premeiotic cells exhibit nuage, a prominent Golgi complex that gives rise to proacrosomal vesicles from the leptotene stage and a flagellimi that is extruded at zygotene. The acrosomal vesicle forms during the round spermatid stage and differentiates into a large and dense basal region and an apical light region. It then migrates while linked to the plasma membrane by its apical pole. Development of the subacrosomal perforatorium is associated with nuage materials and endoplasmic reticulum vesicles. The mature cap-shaped (0.6 μm) acrosomal vesicle exhibits a large apical and irregular region with floccular contents and a basal dense region. The round nucleus becomes barrel-shaped (1.5 μm) and the midpiece (0.8 μm), with four mitochondria, contains a few glycogen particles.     

Structure of filose amoeba <Emphasis Type="Italic">Rhogostoma minus</Emphasis> Belar 1921 (Cryomonadida,Cercozoa) cell

The structure of the unicellular cell of filose amoeba, Rhogostoma minus Belar, 1921, is studied. Zoospores, cysts, and multinuclear plasmodia have not been found. The cell is covered by a thin shell made out of organic matter. Narrow and branched pseudopodia arise from the pseudostome. The vesicle-shaped nucleus, endoplasmic reticulum, microbodies, and Golgi apparatus are of a usual structure. The oval-shaped mitochondria carry tubular cristae. No flagellar apparatus, fibrillar structures, or extrusive organelles have been found. The amoeba feeds on bacteria. The phylogeny of R. minus in regard to other filose amoebas and flagellates is discussed.     

Fine structure of the corpus Luteum of the raccoon during pregnancy

Summary Ultrastructure of the granulosa lutein cells of the raccoon from throughout pregnancy has been described. The lutein cells often from epithelial cords which are separated by the connective tissues, capillaries and lymphatics. Based on the arrangements and modifications of the cytoplasmic organelles and inclusions, three types of lutein cells have been recognized. The type I lutein cells predominantly contain tubular, agranular endoplasmic reticulum, juxtanuclear Golgi complexes, a few round to rod-shaped mitochondria, some free ribosomes, and occasional lipid droplets. Occasionally the tubular cristae of mitochondria and tubular smooth endoplasmic reticulum appear contiguous. The type II cells contain abundant lace-like and/or stacked fenestrated endoplasmic reticulum cisternae that frequently form membranous whorls, some tubular, agranular endoplasmic reticulum, mitochondria, and lipid droplets. Mitochondria are usually small, but unusual large ones also occur. The small, rod-to round-shaped mitochondria usually have tubular cristae; but the large, oval, elongate, and cup shaped mitochondria possess tubular, lamellar, plate like, and whorl-like cristae. The plasma membranes of the cells are complexly elaborated and folded, especially when apposing each other. In favorable sections, strands of fenestrated cisternae appose the folds of the plasma membranes. In general, the amount of cytoplasmic organelles and inclusions vary greatly in the cells. The type III cells predominantly contain lipid droplets and sparse cytoplasmic organelles. The type I and II cells are found throughout pregnancy, but the type III cells are observed from mid gestation to term. The cytological features of type I and II cells suggest that they probably secrete most of the steroids, whereas the type III cells primarily store lipids.This research was supported by UPSHS grant AM-11376 and NIH contract 69-2136.