Cytochemical studies on the antheridial mucilage and changes in its concentration and amount during the spermatogenesis in Chara vulgaris L.

The internal space of the antheridium in Chara vulgaris L. is filled with the PAS-positive mucilage which is of pectic nature. Morphometric and cytophotometric measurements on the semithin sections indicate that the concentration and amount of PAS-positive polysaccharides: 1) increase during the time of antheridial growth accompanying the phase of antheridial filament divisions, 2) these parameters have the maximum after spermatid formation and at the beginning of their differentiation, i.e. spermiogenesis, 3) both concentration and amount of this substance decrease at the end of spermiogenesis. A decrease in mucilage concentration is also observed in the young antheridia after 3 days of continuous darkness. The results suggest that PAS-positive mucilagenous material is a nutritive substance, accumulated in the first phase of antheridial development and utilized mainly in spermiogenesis. These substances may also be used up in the young antheridia during the lack of energy supply. The autoradiographic studies with the use of a 3H-glucose and 3H-galactose mixture seem to confirm these suggestions.     

Symplasmic isolation ofChara vulgaris antheridium and mechanisms regulating the process of spermatogenesis

Summary The antheridium ofChara vulgaris L. is connected by plasmodesmata with the thallusvia a basal cell. Prior to the initiation of spermatozoid differentiation these plasmodesmata are spontaneously broken, resulting in symplasmic isolation of the antheridium.Premature plasmolytically evoked symplasmic isolation of the antheridium leads to a 2–4 fold reduction in the length of antheridial filaments and the elimination of 1–2 cell cycles from the first stage of spermatogenesis.Autoradiographic and cytophotometric studies have shown that, as a result of induced symplasmic isolation of the antheridium, endomitotic DNA synthesis was blocked both in the young manubria (after 24 hours) and in the capitular cells (after 48 hours). In the antheridial filaments DNA synthesis was inhibited together with either elimination of divisions and induction of spermatid differentiation or developmental block. We propose that breakage of plasmodesmata connecting the antheridium with the thallus is a signal which releases, in all antheridia, mechanisms that (i) block endomitotic DNA synthesis in the manubria, (ii) restrict the growth rate and the divisions of antheridial filament cells, and (iii) induce spermiogenesis in these antheridia in which the manubria attained the sufficient level of polyploidy.This work is supported by the Polish Academy of Sciences within the project CPBP 04.01.5.05.     

HETEROTHALLISM AND SEXUALITY IN ASCOBOLUS STERCORARIUS

Bistis, G. N., and J. R. Raper. (Harvard U., Cambridge, Mass.) Heterothallism and sexuality in Ascobolus stercorarius. Amer. Jour. Bot. 50(9): 880–891. Illus. 1963.—The steps in the sexual development of the heterothallic ascomycete, Ascobolus stercorarius, are: (1) induction of antheridial hyphae and antheridia; (2) induction of ascogonial hyphae and ascogonia; (3) directed growth of the trichogyne; and (4) plasmogamy. Although this sequence occurs in each of the 2 reciprocal combinations (A –antheridial/a-ascogonial and a-antheridial/A-ascogonial), several differences between the 2 combinations have been found. The differences are especially apparent with regard to antheridial induction and the pattern of proliferation of ascogonial hyphae. A study of the specificity of the agents regulating the sexual reactions between the 2 mating-types has confirmed previously described class-specificity at antheridial induction (sexual activation). Experiments utilizing substituted oidia have demonstrated an absence of mating-class specificity in trichogyne attraction and even at plasmogamy. The incipient fruiting bodies which result from illegitimate fusions (a X a and A X A), however, stop growing after 24 hr. This cessation of development suggests the presence of a second block to self-fertility in the sexual process of this species.     

DEVELOPMENTAL PROFILES OF GANGLIOSIDES IN HUMAN AND RAT BRAIN

Abstract— The developmental profiles of individual gangliosides of human brain were compared with those of rat brain. Interest was focused mainly on the pre- and early postnatal development. Human frontal lobe cortex covering the period from 10 foetal weeks to adult age and the cerebrum of rat from birth to 21 days were analysed. Lipid-NANA and lipid-P were followed; in the rat, also protein and brain weight. A limited number of samples of human cerebral white matter and cerebellar cortex were also studied. The following major results were obtained:

• 1 The ganglioside concentration increased approximately three-fold within a short period: in rat cerebrum, from birth to the 17th day; in human cerebral cortex, from the 15th foetal week to the age of about 6 months. The largest increase in the rat brain occurred by the 11th to the 13th day; in human brain by term. The relative increase of gangliosides during this period was more rapid than that of phospholipids.
• 2 A hitherto unknown distinct early period of ganglioside and phospholipid formation in rat occurred by the second to fourth day.
• 3 The changes in brain ganglioside pattern, characteristic of the developmental stages of the rat, were found to be equally pronounced in the human brain.
• 4 Regional developmental differences in the ganglioside pattern were demonstrated in human brain. A characteristic white matter pattern, rich in monosialogangliosides, had developed by the age of 1 year. The increase in ganglioside concentration and the formation of the definitive ganglioside pattern of cerebellar cortex occurred later than in cerebral cortex. This cerebellar pattern was characterized by a very large trisialoganglioside fraction.
• 5 The two periods of rapid ganglioside metabolism in rat brain preceded the two periods of rapid protein biosynthesis.

     

Cell sizes and DNA level in antheridial filaments in relation to the initiation of spermatozoid differentiation in Chara vulgaris L

The observations carried out indicate that the exclusion of the S phase initiation from the course of telophase of the last mitotic division in the antheridial filaments of Chara vulgaris, leading to the formation of spermatids is not a simple result of the cell size reduction, gradually accomplished in the course of the successive cell cycles (of S+G2+M type). This critical moment of spermatogenesis is probably induced by the regulators operating at the level of an antheridium. In the conditions of the long (3-5 days) darkness resulting in the cell cycle arrest in antheridial filaments at the early stage of G2 phase there is detected the operation of some additional mechanisms synchronizing spermatogenesis, which enable some retarded antheridial filaments to pass the critical control points and to enter into the process of spermiogenesis insensitive to the lack of the light. The initiation of the differentiation is accomplished either after the cell division induced by the hypothetic inductors of spermiogenesis or -- more rarely -- with omitting mitosis, i.e. in the cells containing 2C DNA.     

Ultrastructural and autoradiographic studies of non-generative cells in the antheridium of Chara vulgaris. I. Manubria

During the development of an antheridium DNA content in manubria gradually increases to 8C-16C level. 3H-thymidine incorporation into the nuclei of the manubria lasts till the stage of quantitative predominance of the 16 celled antheridial filaments. The nucleus of the manubria is characterized by the low content of the condensed chromatin and the presence of nucleoli with the nucleolonema-like structure the number of which increases from 6-8 to 32-38 along with the increase of DNA content in a nucleus. In the cytoplasm of the manubria there are numerous secretive vesicles filled with fine-granular substance discharged outside plasmalemma, active Golgi apparatus, well-developed rough ER, numerous polysomes, mitochondria with the condensed structure and plastids with granar and inter-granar thylakoids as well as plastoglobules which increase in number and size along with the development of the antheridium. During spermiogenesis the cells are vacuolated, the number of the secretive vesicles decreases whereas the electron density of their content increases, smooth ER appears while rough ER is reduced. The manubria actively incorporate 3H-uridine, 3H-tryptophane and 3H-leucine. The increase of the incorporation activity is gradual in the period of increasing polyploidy of the manubria and rapid during the initiation of the spermatozoid differentiation. It has been suggested that the manubria should play an important role in the process of spermatogenesis and the induction of spermatozoid differentiation.     

Plasmodesmal changes are related to different developmental stages of antheridia of Chara species

Summary During the development of the antheridia of Chara species, dynamic changes in the occurrence and ultrastructure of plasmodesmata are observed which are closely correlated to particular developmental phases and presumably regulate the morphogenetic events in the antheridia. The disappearance of plasmodesmata between shield cells and between shied cells and the basal cell leads to a cessation in symplasmic transport around the antheridum and determines its concentric or centrifugal character via centrally situated capitular cells. Unplugged plasmodesmata are present between fully synchronously developing antheridial filament cells and obviously coordinate the development of the cells. In the middle phase of spermiogenesis, rough endoplasmic reticulum in antheridial filaments passes uncompressed through wide plasmodesmata and provides an additional transport pathway for developmental control factors. Plugged plasmodesmata link cells of different types or cells of the same type which are at different phases of cell cycle and guarantee their individual development. The plugging of plasmodesmata is a reversible process that depends on the morphogenetic situation. Plasmodesmata connecting the basal cell and the subbasal cell as well as the basal cell and capitular cells are transformed successively from the simple into the complex type and might be the pathways for an import of gibberellins and nutrients into the strong sink tissues of the developing antheridium. There is a symplasmic connection between the antheridum and the thallus via a basal cell. Prior to the initiation of spermatozoid differentiation (spermiogenesis), plasmodesmata connecting the basal cell with a subbasal cell and the basal cell with capitular cells are spontaneously broken, resulting in symplasmic isolation of the antheridium that is probably a signal which triggers the induction of spermatozoid differentiation. Premature plasmolytically evoked symplasmic isolation of the antheridium leads to the elimination of 1 to 2 cell cycles from the proliferative stage of spermatogenesis. Autoradiographic studies demonstrate that both natural and induced symplasmic isolation drastically decreases the entry of isotopically labeled gibberellic acid into antheridia of Chara species that may be the consequence of the elimination of the hormone's transport through plasmodesmata.Correspondence and reprints: Department of Cytophysiology, University of ód, ulica Pilarskiego 14, 90-231 ód, Poland.Received March 11, 2002; accepted September 19, 2002; published online August 26, 2003     

Differentiated reaction of different types of antheridial cells in Chara vulgaris to the changes in light conditions during 24 hours.

Circadian rhythm of activity of 3H-leucine incorporation into antheridial cells of Chara vulgaris, in natural photoperiod was compared with changes in mitotic activity of antheridial filament cells which form spermatozoids. Three types of cells functionally connected with each other i.e. manubria, capitular cells and antheridial filaments indicate high amplitude (80-90%) changes in circadian translational activity and some similarities in their course. The shield cells are characterized by small circadian changes in translational activity in the range of 15-30% and their different rhythm. Manubria, which are the secretive cells indicated the highest dependence of the dynamic of translational activity on the time of day. Their high activity overlaps light phase, low activity--dark phase. The reaction of capitular cells to day/night change is delayed in comparison with the reaction of manubria, and that of antheridial filaments is delayed in comparison with the capitular cells reaction. The assumption was set forth that manubria play the role of oscillators (starttercells) which induce the wave of changes translocating to the other cells functionally and spatialy connected with them. The course of the wave of antheridial filaments mitotic activity suggests that a distinct drop in MI in the morning may be the result of the lack of the factors necessary for initiation of the mitosis, dependent on light-induced high translational activity of antheridial cells.     

Human immunodeficiency virus-1-tat induces matrix metalloproteinase-9 in monocytes through protein tyrosine phosphatase-mediated activation of nuclear transcription factor NF-kappaB

An appreciable increase in G(M3) with a concomitant decrease in some neolacto-series gangliosides was observed during differentiation of human colonic carcinoma HCT 116 cells induced by a differentiating agent. When the cells were treated with brefeldin A (BFA), a striking increase in de novo biosynthesis of G(M3) and a decrease in biosynthesis of neolactoseries gangliosides were observed after 6 h. Clear morphological changes to differentiated epithelial cells and an arrest of cells in the G0/G1 phase of the cell cycle were observed after 1 day of treatment. Then the cells were led to apoptosis. This activity was not affected by forskolin, which antagonizes the effects of BFA on protein transport and the Golgi apparatus. These results suggest that the differentiation-inducing activity of BFA might be due to its modulatory effect on ganglioside biosynthesis, and that a specific change in ganglioside pattern is an essential prerequisite for induction of differentiation, providing a novel target for differentiation therapy of cancer.     

The development of the guinea pig gallbladder epithelial cells. II. Electron microscopical and enzymhistochemical investigations (author's transl)]

The development of the guinea pig gallbladder epithelium follows a distinct time schedule. During the first phase (up to 30th day of intrauterine life) the epithelial cells increase in number. They remain small and undifferentiated. In the second phase, from the 30th to the 44th day, cytodifferentiation is a dominating feature. The epithelial cells increase in height, the nuclei become more basal, the cells acquire their final zonal structure and the cell organelles exhibit their characteeristic appearance. Weak enzyme activities can be observed. In the third phase, from the 45th day until birth, there is functional differentiation and the adult pattern of enzyme distribution is established. Glycogen appears first on day 29, increases in amount and then disappears by day 57. There is a marked development of the Golgi apparatus associated with increased synthesis of secretory material. Between the 59th embryonic day and the 6th day of life mucoid cells with different functional states appear in the gallbladder epithelium. Later on these cells can be visualized only in the depths of the invaginations. After birth the epithelial cells become more columnar and by 10 days after birth the adult appearance of the epithelium is fully established.     

Fine structure of antheridia and oogonia of Phytophthora macrospora,the downy mildew fungus of rice plants

In the present paper fine structure of antheridium and oogonium ofPhytophthora macrospora (Sacc.)S. Ito etI. Tanaka, the downy mildew fungus of rice plants was discussed.Before the fertilization some nuclei and a large number of mitochondria were scattered in the cytoplasm of the antheridium. Many lipid granules were observed in the peripheral region, but vacuoles did not appear at this stage of antheridium. Many mitochondria were associated in the neighborhood of the fertilization pore. The wall at the pore was very thin, but the wall surrounding the pore was slightly swollen towards the inside.In the oogonium, many nuclei, mitochondria and cytoplasmic matrix were observed at the peripheral part. A large number of lipid granules was found in the oogonium, but they were more numerous in the peripheral region. The vacuoles developed as the oogonium matured. They were enveloped by tonoplast and contained vacuolar matrix. Many electron dense granules were in contact with the tonoplast or free in the vacuoles, and they were larger in the central part. As stated above, wall at the fertilization pore was thin. However, the oogonial wall surrounding the pore swelled protruding into the oogonium. An electron-dense layer was recognized between the antheridial and oogonial wall, and the walls of both the organs were closely in contact with each other.Contribution No. 252.     

ANTHERIDIAL FORMATION IN ONOCLEA SENSIBILIS L.: GENESIS OF THE JACKET CELL WALLS

Antheridial initiation in Onoclea sensibilis L., an advanced leptosporangiate fern, begins with the production of a small, wedge-shaped cell within the anterior region of the vegetative cell. This is in contrast to previous reports claiming that the initials are formed by a localized protuberance in the cell wall of the vegetative cell (Campbell, 1886; Davie, 1951; Leung and Naf, 1979; Nayar and Kaur, 1971). The mature antheridium of Onoclea is composed of three uniquely shaped jacket cells surrounding spermatogenous cells. The two funnel-shaped jacket cell walls are shown to form in a lateral circular manner. Except for the production of the antheridial initial cell, jacket cell formation in Onoclea proceeds in accordance with the classical concept of antheridial development in advanced ferns accredited in part to Atkinson (1894), Campbell (1886), Kny (1869), and Strasburger (1869). The classical concept has been contested in more recent years by Davie (1951), Leung and Näf (1979), and Verma and Khullar (1966).     

On the physiology and chemistry of fern antheridiogens

Döpp has demonstrated an antheridium-inducing hormone (antheridiogen) in P.aquilinum. This antheridiogen (abbr. Apt.) is active in many, if not all, species of the family Polypodiaceae. Among responsive species, the minimally effective concentration varies widely. Apt was assayed againstOnoclea sensibilis because this species fails to form antheridia spontaneously under the prevailing conditions of culture and because none of the many species tested responds to a lower concentration A_Pt is inactive toward the investigated species of the fern families Osmundaceae, Cyatheaceae and Schizaeaceae. The two schizaeaceous speciesAnema phyllitidis andLygodium japonicum also elaborate antheridiogens (abbr. A_An and A_Ly). Both these antheridiogens are inactive in 0.sensibilis, the species used to assay for A_Pt. A_An, A_Ly, A_Pt and A_On (the antheridiogen of O.sensibilis) are distinct entities based both on the criteria of cross-testing and of Chromatographic separation. Cross-testing led to the conclusion that the antheridiogen ofCeratopteris thalictroides differ from A_Pt and A_An. Gibberellins have antheridiogenic properties in schizaeaceous species but, like A_An and A_Ly, they fail to hasten antheridium formation in the species used to assay for A_Pt. The native antheridiogens of schizaeaceous species are more species-selective in their action than is GA₃. A_An has recently been isolated. Its structure is similar to, if not identical with, that of gibberellins. A_An behaves like a weak gibberellin in several higher plant assay systems. The prothalli ofP. aquilinum andO. sensibilis become insensitive to Apt as they attain heart shape or shortly thereafter. Prothalli ofP. aquilinum do not begin to synthesize A_Pt and secrete it into the medium, until after they have become insensitive to it. It is in consequence of this that the most rapidly growing and developing individuals attain the archegonial phase without a prior antheridial phase. Various mechanisms and developmental characteristics are described, which strongly favor cross-fertilization inP. aquilinum without, however, eliminating an opportunity for self-fertilization. The cells of abortive antheridium initials, and of “green antheridia”, exhibit certain characteristics of green vegetative cells. These atypical structures appear to arise when early antheridial stages are overtaken by conditions unfavorable to antheridium differentiation. The observations suggest that A_Pt may be required beyond an initial inductive event. The investigations led to the conclusion that A_Pt functions by cancelling a light-dependent block to antheridium formation and suggest that in darkness this block decays without the intervention of A_Pt. InPolypodium crassifolium, the light-effect on antheridium formation is mediated by phytochrome. Other subject matters discussed include: The cellular location of antheridium initials; the relationship of antheridiogen to antheridiogen structure; the existence of a switching mechanism in the sexual development ofO. sensibilis; the retrieval of genetic information in the induction and differentiation of antheridia; the tempero-spatial pattern of competence to antheridiogen in schizaeaceous species and the inducibility of a physiological state antagonistic to antheridium formation in A.phyllitidis.     

Biological role of endoreplication in the process of spermatogenesis inChara vulgaris L.

Summary During cell division in antheridial filaments ofChara vulgaris an increase in DNA content occurs in both shield cells and manubria within an antheridium, reaching 16C–64C and 8C–32C levels, respectively. Endoreplication ceases prior to the formation of spermatids and initiation of spermiogenesis, probably as a result of symplasmic isolation of the antheridium from the thallus. As the DNA content of the nuclei increases, the shield cells³H-leucine incorporation increases, and they grow intensively in the tangential plane. Translation decreases considerably after termination of shield cell growth. DNA content of mature manubria is half of that in shield cells, although their size is 10 times that of manubria. Translational activity of manubria also increases as DNA content rises and cells grow. However, during spermiogenesis, this activity remains at its maximum, which is associated with the secretory function of the manubria. Spermiogenesis is also accompanied by far-reaching ultrastructural changes within the manubrial cytoplasm.The level of endopolyploidy in both shield cells and manubria of antheridia formed in the spring is higher by one replication cycle, than in autumnal antheridia. AMO-1618, at a concentration of 10^–5M reduces the DNA content in the autumnal manubria. The higher the manubrial level of endopolyploidy in spermiogenesis, the greater their size, and the higher the translational activity and number of joined spermatids. The number of spermatozoids in the antheridium is also positively correlated with the internal volume of an antheridium, which is itself dependent on the endopolyploidy level of shield cells.The results obtained confirm the assumption that endoreplication favours the higher growth dynamics and potential translational activity, which occurs in the dynamic growth phase only in shield cells, while in manubria, i.e. cells producing substances necessary to spermatozoids development, it remains high until the end of spermiogenesis.     

MICROGAMETOPHYTE DEVELOPMENT IN THE PALEOZOIC SEED FERN FAMILY CALLISTOPHYTACEAE

Well-preserved stages of microgametophyte development are described from pollen produced by the Paleozoic seed fern family Callistophytaceae. Microgametophyte development in both the Middle Pennsylvanian pollen organ Idanothekion and Upper Pennsylvanian Callandrium involved the initial production of an axial row of at least three small prothallial cells proximally and a large embryonal cell distally. The arrangement and form of these cells is like that present in some extant genera of the Pinaceae. The prothallial cells were relatively large in comparison with extant gymnosperms, occupying the entire region of the cap-pus, and were apparently all primary. Evidence is presented that in Callandrium further development involved an anticlinal division of the large distal cell (antheridial initial) into a small generative cell contained within a larger tube cell. Previously described microgametophytes of the late Paleozoic order Cordaitales are reinterpreted and are shown to consist of an embryonal cell and three to four discoidal prothallial cells in an axial row like that of the Callistophytaceae. Microgametophytes thus far described from the Paleozoic are remarkably modern in appearance and provide no evidence to support the generally held view that the seed plant microgametophyte is an extremely reduced sexual phase that has arisen through the loss of almost all of the vegetative cells and the sterile outer cells of the antheridium. Evidence to support or refute this view will depend upon the discovery of microgametophytes from older groups of seed plants than those for which they are now known.     

ON THE RELEASE OF SPERMS IN ATRICHUM

An antheridium of Atrichum contracts when it opens. This contraction rapidly ejects much of the mass of sperms because a fluid present in the base of the antheridial chamber acts as an hydraulic ram. The residue of sperms is slowly extruded as the same fluid takes up water. Photographs allow the construction of time courses that directly demonstrate the existence of two phases (rapid vs. slow) in sperm release. Antheridia open as quickly in 1 m sucrose as they do in water. Molar sucrose allows only the rapid phase of sperm release, caused by the contraction of the jacket, and the antheridia remain only partly emptied. This behavior in sucrose solution provides a convenient test for similarities among antheridia. The mechanism of sperm release that occurs in Atrichum occurs in Polytrichum and Mnium as well.     

Die Steuerung der Antheridienbildung in Polypodium crassifolium L. (Pessopteris crassifolia Underw. and Maxon) durch Licht

Summary In Polypodium crassifolium, light controls the induction of antheridium formation in contrast to hormonal induction in other fern species.Antheridium formation is caused by an exposure to darkness or far-red. The minimum duration of this treatment required to bring about antheridium formation depends on the length of preillumination with white light.Red light interruptions of 5 min (6,6 E cm^-2 sec^-1) at 24 h intervals applied during the whole dark period extinguish antheridium induction. Red light inhibition is cancelled by a succeeding irradiation with far-red.Inhibitors of protein and nucleic acid synthesis do not block antheridium induction. Actinomycin-D inhibits the formation of spermatogenic tissue.The results presented indicate a control of antheridium formation in Polypodium crassifolium via a negative photoresponse (Mohr, 1966). So ist appears highly improbable that this differentiation process is based on a specific gene activation in the sense of Jacob and Monod.     

葫芦藓精子发生过程中胞间连丝与胞质桥的超微结构

从超微结构水平上对葫芦藓(Funaria hygrometrica Hedw.)精子发生过程中胞间连接系统的结构及其变化动态进行了研究.结果表明,同一区中的相邻生精细胞由大量胞质桥相连,而不同区的细胞之间则不存在胞质桥.胞间连丝存在于套细胞之间以及套细胞与生精细胞之间,但它在生精细胞间不存在.在精子器发生的后期,当精子细胞壁开始降解时,同一个精子器中所有的精子细胞似乎都由扩大的胞质桥相互连接.胞质桥一直保持到精子分化的后期,最终精子细胞同步分化成精子.胞间连丝与胞质桥具有不同的内部结、分布以及生物发生机制,这表明它们在精子器的发育过程中可能扮演着不同的角色.     

Electron microscopy of gametangial interaction and oospore development in Phytophthora capsici

Gametangial development and oospore formation were studied, with emphasis on cell wall morphogenesis, on mated cultures (A¹xA²) of Phytophthora capsici. In this species, the oogonial and antheridial hyphae interact to produce a typical amphigynous antheridium. The following developmental steps were recognized: 1) contact between oogonial and antheridial initials; 2) penetration of the antheridial initial by the oogonial initial; 3) reemergence of the oogonial initial; 4) oogonial expansion; 5) gametangial delimitation and oogonial wall thickening; 6) penetration of the oogonium by the antheridial fertilization tube; 7) oosphere formation; 8) periplasm degeneration and outer oospore wall formation; and 9) inner oospore wall formation. Electron micrographs were obtained of steps 3–9. Steps 1 and 2 were reconstructed from subsequent events. Steps 3–6 are stages of active wall formation with clear indication of intensive dictyosome activity leading to the formation of numerous wall-destined vesicles of two different sizes and electron densities. No vesicles were seen associated with the development of the inner oospore wall; however, by this stage of development the oosphere cytoplasm exhibited an overall intense electron density that obscured fine detail. Cytoplasmic appearance changed enormously during differentiation, from a developing oogonium rich in mitochondria, ribosomes, rough endoplasmic reticulum, dictyosomes and their vesicles, through an oosphere filled with large finger-print vacuoles and lipid-like bodies, to a mature oospore with a large central vacuole (ooplast) surrounded by a cortex of numerous lipid-like bodies; other organelles are confined to the interstitial space between these storage bodies.     

Changes in mRNA levels of rat pancreatic lipase in the early days of consumption of a high-lipid diet

The time-course response of rat pancreatic enzymes to a diet containing 25% sunflower oil was investigated. A 1.2-fold enhancement in lipase specific activity was observed as early as the first day of diet consumption and was further increased up to 1.9-fold on the 5th day. On the other hand, colipase activity was slightly decreased during the first two days of high-lipid diet intake and then increased. An immediate and direct effect was also exerted by the 25% lipid diet on lipase biosynthesis. Both fractional synthetic rate and specific activity of lipase were comparably induced. Due to a 1.6-fold increase in the overall protein synthesis following 5 days of lipid diet consumption, the absolute synthesis of lipase and amylase was increased by 3.5-fold and 0.98-fold, respectively, as compared to control animals. By contrast, the synthesis of procarboxypeptidases and serine proteases did not increase before day 5, probably as the result of a distinct adaptive mechanism. The pancreatic mRNA levels in control and adapted animals, which were determined by dot-blot hybridization with amylase and lipase cDNAs, were consistent with a biphasic induction of lipase synthesis since a first increase in the level of the enzyme-specific mRNA during the first two days of diet intake (4-fold on day 1) was followed by a second increase after the fourth day (6.5-fold on day 5). On the other hand, amylase mRNA level was unchanged during the dietary manipulation. Thus, hyperlipidic diets exerted an both lipase activity and synthesis but a delayed effect on procarboxypeptidase and serine protease synthesis. In a similar manner, the immediate induction of lipase mRNA level by dietary fat, followed by another increase a few days later, suggested that at least two different mechanisms are involved in lipase mRNA induction.