Pub Date : 1985-07-01DOI: 10.1016/0889-1605(85)90129-6
Willem G. Langenberg
In thin sections of wheat cells doubly infected with wheat spindle streak mosaic (WSSMV) and soil-borne wheat mosaic viruses (SBWMV), virions and inclusion bodies of both viruses all reacted with antiserum to SBWMV virions. Only the WSSMV virions reacted with antiserum to WSSMV virions. Anti-SBWMV IgG reacted only with SBWMV virions and not with WSSMV virions in leaf-dip preparations from doubly infected plants. The anomalous results can be explained byin vivo SBWMV capsid or inclusion body protein association with both WSSM virions and WSSMV-induced pinwheels and scrolls as well as with its own virions and inclusion bodies. Wheat spindle streak mosaic virus reacted with anti-barley yellow mosaic virus IgG in tissue sections and in leaf-dip preparations. Goat-anti-rabbit IgG labeled with colloidal gold remained active and useful after 14 months storage at 4°C in protection buffer.
{"title":"Immunoelectron microscopy of wheat spindle streak and soil-borne wheat mosaic virus doubly infected wheat","authors":"Willem G. Langenberg","doi":"10.1016/0889-1605(85)90129-6","DOIUrl":"https://doi.org/10.1016/0889-1605(85)90129-6","url":null,"abstract":"<div><p>In thin sections of wheat cells doubly infected with wheat spindle streak mosaic (WSSMV) and soil-borne wheat mosaic viruses (SBWMV), virions and inclusion bodies of both viruses all reacted with antiserum to SBWMV virions. Only the WSSMV virions reacted with antiserum to WSSMV virions. Anti-SBWMV IgG reacted only with SBWMV virions and not with WSSMV virions in leaf-dip preparations from doubly infected plants. The anomalous results can be explained by<em>in vivo</em> SBWMV capsid or inclusion body protein association with both WSSM virions and WSSMV-induced pinwheels and scrolls as well as with its own virions and inclusion bodies. Wheat spindle streak mosaic virus reacted with anti-barley yellow mosaic virus IgG in tissue sections and in leaf-dip preparations. Goat-anti-rabbit IgG labeled with colloidal gold remained active and useful after 14 months storage at 4°C in protection buffer.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"92 1","pages":"Pages 72-79"},"PeriodicalIF":0.0,"publicationDate":"1985-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0889-1605(85)90129-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72231039","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-07-01DOI: 10.1016/0889-1605(85)90125-9
Roland Foisner , Kurt Messner , Herbert Stachelberger , Max Roehr
Transmission electron microscopic investigations revealed extracellular three-lamellar and tubuli-like structures formed by the white rot fungusSporotrichum pulverulentum, which was grown with glucose on a rotary shaker. These structures, originating from the outermost fungal cell wall layer, were isolated by digesting the purified cell walls with snail enzyme. The resistant structures contained in the outer cell wall layer were harvested and chemically analyzed. They were composed of 80–90% carbohydrates, primarily glucose monomeres; 5–10% proteins, including five fractions with molecular weights between 30 000 and 200 000; and, finally, 5–10% lipids, none of which were phospholipids. Chemical analysis of the components after treatment with 2-mercaptoethanol/EDTA, followed by TEM observations, however, suggests that these structures consist of almost equal amounts of carbohydrate, protein, and lipid and that the additional carbohydrate is attached to them without any structural function. Several hypothesis concerning the biological function of the structures are made.
{"title":"Isolation and characterization of extracellular three-lamellar structures ofSporotrichum pulverulentum","authors":"Roland Foisner , Kurt Messner , Herbert Stachelberger , Max Roehr","doi":"10.1016/0889-1605(85)90125-9","DOIUrl":"https://doi.org/10.1016/0889-1605(85)90125-9","url":null,"abstract":"<div><p>Transmission electron microscopic investigations revealed extracellular three-lamellar and tubuli-like structures formed by the white rot fungus<em>Sporotrichum pulverulentum</em>, which was grown with glucose on a rotary shaker. These structures, originating from the outermost fungal cell wall layer, were isolated by digesting the purified cell walls with snail enzyme. The resistant structures contained in the outer cell wall layer were harvested and chemically analyzed. They were composed of 80–90% carbohydrates, primarily glucose monomeres; 5–10% proteins, including five fractions with molecular weights between 30 000 and 200 000; and, finally, 5–10% lipids, none of which were phospholipids. Chemical analysis of the components after treatment with 2-mercaptoethanol/EDTA, followed by TEM observations, however, suggests that these structures consist of almost equal amounts of carbohydrate, protein, and lipid and that the additional carbohydrate is attached to them without any structural function. Several hypothesis concerning the biological function of the structures are made.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"92 1","pages":"Pages 36-46"},"PeriodicalIF":0.0,"publicationDate":"1985-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0889-1605(85)90125-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72231041","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-07-01DOI: 10.1016/0889-1605(85)90128-4
Xavier Mattei, Bernard Marchand, Claudine Mattei
The hemoglobin of the lizardTarentola annularis has been studied within erythrocytes being digested in the gut of a parasitic pentastomide,Raillietiella sp. The hemoglobin is crystallized in the form of bundles comprised of numerous tubules (up to 2000). These tubules are simple or complex. Simple tubules are 50 nm in diameter; their wall is made up of two electron-opaque rings, separated by a clear ring. Complex tubules are up to 100 nm in diameter and show as many as 13 concentric walls. High magnification of transverse sections of simple tubules show 96 granules; each opaque ring is made up of 48 granules. Human hemoglobin is known to crystallize as 18-nm tubules, the wall of which is made up of six molecules; comparison of these data with our observations indicates that transverse sections of tubules of crystallized lizard hemoglobin should contain 24 molecules. Thus, each molecule of crystallized lizard hemoglobin consists of four granules; these granules may be considered as globin molecules. Erythrocytes in fresh lizard blood do not show crystallized hemoglobin; however, in blood treated with sodium bisulfite, they show tubules similar to that found in the parasite.
{"title":"Cristallisation de l'he´moglobine d'un reptile au cours de sa digestion chez un pentastomide","authors":"Xavier Mattei, Bernard Marchand, Claudine Mattei","doi":"10.1016/0889-1605(85)90128-4","DOIUrl":"https://doi.org/10.1016/0889-1605(85)90128-4","url":null,"abstract":"<div><p>The hemoglobin of the lizard<em>Tarentola annularis</em> has been studied within erythrocytes being digested in the gut of a parasitic pentastomide,<em>Raillietiella</em> sp. The hemoglobin is crystallized in the form of bundles comprised of numerous tubules (up to 2000). These tubules are simple or complex. Simple tubules are 50 nm in diameter; their wall is made up of two electron-opaque rings, separated by a clear ring. Complex tubules are up to 100 nm in diameter and show as many as 13 concentric walls. High magnification of transverse sections of simple tubules show 96 granules; each opaque ring is made up of 48 granules. Human hemoglobin is known to crystallize as 18-nm tubules, the wall of which is made up of six molecules; comparison of these data with our observations indicates that transverse sections of tubules of crystallized lizard hemoglobin should contain 24 molecules. Thus, each molecule of crystallized lizard hemoglobin consists of four granules; these granules may be considered as globin molecules. Erythrocytes in fresh lizard blood do not show crystallized hemoglobin; however, in blood treated with sodium bisulfite, they show tubules similar to that found in the parasite.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"92 1","pages":"Pages 63-71"},"PeriodicalIF":0.0,"publicationDate":"1985-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0889-1605(85)90128-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72230959","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-06-01DOI: 10.1016/S0022-5320(85)80016-2
Pyoyun Park, Tohgo Ohno
Unusual structures often found in the cytoplasm of tumor cells in a clear-cell sarcoma appeared as multilayered, concentric, oval, spiral, parallel arrays of cisternae in various planes of section. It was demonstrated that the cisternal membrane and cavity were continuous with plasmalemmas of tumor cells and the extracellular space, respectively, suggesting that the structures were formed by the intracytoplasmic infoldings of plasmalemmas. Another characteristic found in the structures was orderly microfilaments with an average diameter of 6.5 nm which were placed between the confronting plasmalemmas in the infoldings. The filaments which underlay the infolded plasmalemmas ran parallel to each other along the cytoplasmic surfaces of plasmalemmas approximately 15 nm apart. The regularly arranged filaments were found in the infolded plasmalemmas, but not beneath any other area of plasmalemmas. The short ends of long filaments appeared to bend toward the inner surfaces of plasmalemma and to be directly connected with the surface proper. These results show that the filaments may be closely associated with the plasmalemmal infoldings and included as the same category of plasmalemmal undercoat. Additionally, the biological significance of the structures is discussed.
{"title":"Microfilament-undercoated plasmalemmal infoldings in a human clear-cell sarcoma","authors":"Pyoyun Park, Tohgo Ohno","doi":"10.1016/S0022-5320(85)80016-2","DOIUrl":"10.1016/S0022-5320(85)80016-2","url":null,"abstract":"<div><p>Unusual structures often found in the cytoplasm of tumor cells in a clear-cell sarcoma appeared as multilayered, concentric, oval, spiral, parallel arrays of cisternae in various planes of section. It was demonstrated that the cisternal membrane and cavity were continuous with plasmalemmas of tumor cells and the extracellular space, respectively, suggesting that the structures were formed by the intracytoplasmic infoldings of plasmalemmas. Another characteristic found in the structures was orderly microfilaments with an average diameter of 6.5 nm which were placed between the confronting plasmalemmas in the infoldings. The filaments which underlay the infolded plasmalemmas ran parallel to each other along the cytoplasmic surfaces of plasmalemmas approximately 15 nm apart. The regularly arranged filaments were found in the infolded plasmalemmas, but not beneath any other area of plasmalemmas. The short ends of long filaments appeared to bend toward the inner surfaces of plasmalemma and to be directly connected with the surface proper. These results show that the filaments may be closely associated with the plasmalemmal infoldings and included as the same category of plasmalemmal undercoat. Additionally, the biological significance of the structures is discussed.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"91 3","pages":"Pages 232-242"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-5320(85)80016-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15204917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-06-01DOI: 10.1016/S0022-5320(85)80012-5
R. Kessel
{"title":"The relationships of annulate lamellae, fibrogranular bodies, nucleolus, and polyribosomes during spermatogenesis in Drosophila melanogaster","authors":"R. Kessel","doi":"10.1016/S0022-5320(85)80012-5","DOIUrl":"https://doi.org/10.1016/S0022-5320(85)80012-5","url":null,"abstract":"","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"64 1","pages":"183-191"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75209479","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-06-01DOI: 10.1016/S0022-5320(85)80015-0
William C. Hamlett , John P. Wourms , Joan S. Hudson
During mid- and late gestation, the uterus of sandbar sharks possesses specialized sites for exchange of metabolites between the mother and fetus. Attachment sites are highly vascular, rugose elevations of the maternal uterine lining that interdigitate with the fetal placenta. The maternal epithelium remains intact and there is no erosion. The attachment site consists of a simple, low columnar juxtaluminal epithelium underlain by an extensive vascular network. Juxtaluminal epithelial cells possess branched microvilli, saccular invaginations of the apical surface, and coated pits. They contain numerous coated vesicles, lipid-like inclusions, a prominent rough endoplasmic reticulum, and many free ribosomes. Tight junctions join the luminal aspect of adjacent cells. Lateral cell boundaries are highly folded and interdigitated. Capillaries are closely apposed to the basal cell surfaces. The endothelium is pinocytotically active. Comparison with the uterine epithelium of non-placental sharks, mammalian epitheliochorial placentae, and selected transporting epithelia reveals that the structure of the maternal shark placenta is consistent with its putative multiple functions, viz.: (1) nutrient transfer; (2) transport of macromolecules, e.g., immunoglobulins; (3) respiration; and (4) osmotic and ionic regulation.
{"title":"Ultrastructure of the full-term shark yolk sac placenta","authors":"William C. Hamlett , John P. Wourms , Joan S. Hudson","doi":"10.1016/S0022-5320(85)80015-0","DOIUrl":"https://doi.org/10.1016/S0022-5320(85)80015-0","url":null,"abstract":"<div><p>During mid- and late gestation, the uterus of sandbar sharks possesses specialized sites for exchange of metabolites between the mother and fetus. Attachment sites are highly vascular, rugose elevations of the maternal uterine lining that interdigitate with the fetal placenta. The maternal epithelium remains intact and there is no erosion. The attachment site consists of a simple, low columnar juxtaluminal epithelium underlain by an extensive vascular network. Juxtaluminal epithelial cells possess branched microvilli, saccular invaginations of the apical surface, and coated pits. They contain numerous coated vesicles, lipid-like inclusions, a prominent rough endoplasmic reticulum, and many free ribosomes. Tight junctions join the luminal aspect of adjacent cells. Lateral cell boundaries are highly folded and interdigitated. Capillaries are closely apposed to the basal cell surfaces. The endothelium is pinocytotically active. Comparison with the uterine epithelium of non-placental sharks, mammalian epitheliochorial placentae, and selected transporting epithelia reveals that the structure of the maternal shark placenta is consistent with its putative multiple functions, viz.: (1) nutrient transfer; (2) transport of macromolecules, e.g., immunoglobulins; (3) respiration; and (4) osmotic and ionic regulation.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"91 3","pages":"Pages 221-231"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-5320(85)80015-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72286251","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-06-01DOI: 10.1016/S0022-5320(85)80014-9
William C. Hamlett , John P. Wourms , JoAn S. Hudson
The smooth, proximal portion of the yolk sac placenta of the sandbar shark, Carcharhinus plumbeus is comprised of: (1) An outermost epithelial ectoderm; (2) an intervening collagenous stroma; and (3) an inner mesothelium. The surface epithelium may be one to three cell layers thick. The surface epithelium comprises two cell types. A cuboidal cell that has a dome-like apical surface covered with microvilli and an ovoid nucleus predominate. These cells contain lipid inclusions, many cytoplasmic filaments, and are joined by desmosomes. The second cell type has a convoluted nucleus and a flattened cell apex with microvilli, cilia, and paddle cilia. Golgi complexes and elements of the endoplasmic reticulum are relatively uncommon in the cytoplasm of both cell types. Microplicae also occur on the surfaces of some cells. The smooth, proximal portion of the placenta is sparsely vascularized. The innermost cellular elements of the surface epithelium rest on a prominent basal lamina. A collagenous zone separates the epithelial basal lamina from the basal lamina of the mesothelium. The mesothelial cells are squamous with a fusiform nucleus, many pinocytotic pits and vesicles, and a large number of cytoplasmic filaments. The endoplasmic reticulum, except for occasional patches of the rough type, and the Golgi complex are poorly developed. Ultrastructural tracer studies show that this portion of the placenta does not absorb horseradish peroxidase (HRP) and trypan blue.
{"title":"Ultrastructure of the full-term shark yolk sac placenta","authors":"William C. Hamlett , John P. Wourms , JoAn S. Hudson","doi":"10.1016/S0022-5320(85)80014-9","DOIUrl":"https://doi.org/10.1016/S0022-5320(85)80014-9","url":null,"abstract":"<div><p>The smooth, proximal portion of the yolk sac placenta of the sandbar shark, <em>Carcharhinus plumbeus</em> is comprised of: (1) An outermost epithelial ectoderm; (2) an intervening collagenous stroma; and (3) an inner mesothelium. The surface epithelium may be one to three cell layers thick. The surface epithelium comprises two cell types. A cuboidal cell that has a dome-like apical surface covered with microvilli and an ovoid nucleus predominate. These cells contain lipid inclusions, many cytoplasmic filaments, and are joined by desmosomes. The second cell type has a convoluted nucleus and a flattened cell apex with microvilli, cilia, and paddle cilia. Golgi complexes and elements of the endoplasmic reticulum are relatively uncommon in the cytoplasm of both cell types. Microplicae also occur on the surfaces of some cells. The smooth, proximal portion of the placenta is sparsely vascularized. The innermost cellular elements of the surface epithelium rest on a prominent basal lamina. A collagenous zone separates the epithelial basal lamina from the basal lamina of the mesothelium. The mesothelial cells are squamous with a fusiform nucleus, many pinocytotic pits and vesicles, and a large number of cytoplasmic filaments. The endoplasmic reticulum, except for occasional patches of the rough type, and the Golgi complex are poorly developed. Ultrastructural tracer studies show that this portion of the placenta does not absorb horseradish peroxidase (HRP) and trypan blue.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"91 3","pages":"Pages 207-220"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-5320(85)80014-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72247187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-06-01DOI: 10.1016/S0022-5320(85)80018-6
{"title":"Author index for volume 91","authors":"","doi":"10.1016/S0022-5320(85)80018-6","DOIUrl":"https://doi.org/10.1016/S0022-5320(85)80018-6","url":null,"abstract":"","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"91 3","pages":"Page 276"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-5320(85)80018-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72286232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-06-01DOI: 10.1016/S0022-5320(85)80017-4
{"title":"Abstracts from the thirty-eighth annual meeting of the scandinavian society for electron microscopy","authors":"","doi":"10.1016/S0022-5320(85)80017-4","DOIUrl":"https://doi.org/10.1016/S0022-5320(85)80017-4","url":null,"abstract":"","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"91 3","pages":"Pages 243-275"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-5320(85)80017-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72286231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1985-06-01DOI: 10.1016/S0022-5320(85)80012-5
Richard G. Kessel
Irregularly shaped masses of electron-dense material that are located in the perinuclear cytoplasm of Drosophila spermatocytes contain small granular and fibrillar subunits. These fibrogranular bodies can be observed to extend toward and into the nuclear pores where the material is also continuous with nucleolar material. These observations further substantiate a nucleolar origin for the fibrogranular bodies. As pores of annulate lamellae differentiate within the fibrogranular bodies, structural configurations resembling polyribosomes are noted. Microtubules can also be observed in the fibrogranular material and in some cases they are close to differentiated pores of annulate lamellae. These morphological observations tend to confirm and extend previous suggestions that the fibrogranular bodies may represent stored gene products, and that the differentiation of pores is associated with the dispersal, processing, and assembly of the material perhaps in the form of special functioning polyribosomes. The studies also raise the question of whether or not tubulin may be one of the proteins synthesized by these newly formed polyribosomes.
{"title":"The relationships of annulate lamellae, fibrogranular bodies, nucleolus, and polyribosomes during spermatogenesis in Drosophila melanogaster","authors":"Richard G. Kessel","doi":"10.1016/S0022-5320(85)80012-5","DOIUrl":"https://doi.org/10.1016/S0022-5320(85)80012-5","url":null,"abstract":"<div><p>Irregularly shaped masses of electron-dense material that are located in the perinuclear cytoplasm of <em>Drosophila</em> spermatocytes contain small granular and fibrillar subunits. These fibrogranular bodies can be observed to extend toward and into the nuclear pores where the material is also continuous with nucleolar material. These observations further substantiate a nucleolar origin for the fibrogranular bodies. As pores of annulate lamellae differentiate within the fibrogranular bodies, structural configurations resembling polyribosomes are noted. Microtubules can also be observed in the fibrogranular material and in some cases they are close to differentiated pores of annulate lamellae. These morphological observations tend to confirm and extend previous suggestions that the fibrogranular bodies may represent stored gene products, and that the differentiation of pores is associated with the dispersal, processing, and assembly of the material perhaps in the form of special functioning polyribosomes. The studies also raise the question of whether or not tubulin may be one of the proteins synthesized by these newly formed polyribosomes.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"91 3","pages":"Pages 183-191"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-5320(85)80012-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72283833","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}