The Morphology and Origin of the Golgi Bodies and their Role in the Secretion of the Acrosome in the Spermatogenesis of Pulmonate Gastropods as Determined in the Living Material by Phase-contrast Microscopy

1956 ◽  
Vol s3-97 (39) ◽  
pp. 369-377
Author(s):  
VISHWA NATH ◽  
BRIJ L. GUPTA

In this paper are embodied our observations on the morphology, origin, and role of the Golgi bodies in the spermatogenesis of the slug, Anadenus altivagus, and the snail, Euaustenia cassida. Living cells have been studied under the phase-contrast microscope and photomicrographed. In the juxta-nuclear Golgi region in primary spermatocytes the Golgi bodies exist in the form of (1) granules and rods of dark contrast, (2) spheres of pale contrast, and (3) spheroids showing a duplex structure, each consisting of a sphere of pale contrast and an incomplete or complete cortex or sheath of dark contrast. The Golgi spheroids have been shown to arise three times in the course of spermatogenesis from the mitochondrial granules by a process of alignment. The acrosome is formed from a cap of tiny acrosomal granules, which are deposited in front of the spermatid nucleus by the Golgi bodies (acroblasts).

1956 ◽  
Vol s3-97 (38) ◽  
pp. 171-176
Author(s):  
RAJINDER RISHI

Golgi bodies in the living liver-cells of the slug, Anadenus altivagus, exist in two forms: (a) homogeneous granules or spheres of dark contrast, and (b) spheres showing a duplex structure with a light greyish internum and a dark externum, which may be single or composite. The greyish internum of these duplex spheroids grows into the secretory granules, the dark externum disappearing in the process of growth. Mitochondria appear as fibres of light greyish contrast with a dark granule at each tip. This dark granule disassociates itself from the mitochondrion and forms the Golgi granule of dark contrast--the Golgi ‘pre-substance’. The Golgi pre-substance, stainable with neutral red, forms the Golgi spheroids.


2021 ◽  
Vol 11 (11) ◽  
pp. 4985
Author(s):  
Gianluigi Caccianiga ◽  
Gérard Rey ◽  
Paolo Caccianiga ◽  
Alessandro Leonida ◽  
Marco Baldoni ◽  
...  

The aim of this study was to evaluate two different kinds of rough implant surface and to assess their tendency to peri-implantitis disease, with a follow-up of more than 10 years. Data were obtained from a cluster of 500 implants with Ti-Unite surface and 1000 implants with Ossean surface, with a minimum follow-up of 10 years. Implants had been inserted both in pristine bone and regenerated bone. We registered incidence of peri-implantitis and other causes of implant loss. All patients agreed with the following maintenance protocol: sonic brush with vertical movement (Broxo), interdental brushes, and oral irrigators (Broxo) at least two times every day. For all patients with implants, we evaluated subgingival plaque samples by phase-contrast microscopy every 4 months for a period of more than 10-years. Ti-Unite surface implants underwent peri-implantitis in 1.6% of the total number of implants inserted and Ossean surface implants showed peri-implantitis in 1.5% of the total number of implants. The total percentage of implant lost was 4% for Ti-Unite surfaces and 3.6% for Ossean surfaces. Strict control of implants leads to low percentage of peri-implantitis even for rough surfaces dental implants.


1962 ◽  
Vol 12 (1) ◽  
pp. 1-15 ◽  
Author(s):  
Richard M. Franklin

A correlation of cytochemical changes with virus production has been studied in L cells infected with Mengovirus. After a latent period of about 2 hours, virus was produced rapidly, reaching maximum titers of up to 12,000 particles per cell in 6 to 8 hours. The earliest cytological change was in the nucleus and consisted of a slight condensation of chromatin. There is no evidence, however, for the multiplication of either the viral RNA or protein in the nucleus. RNA, of high molecular weight, accumulated in the perinuclear area of the cytoplasm and was later found in inclusions. The perinuclear RNA was digestible with RNase and may be located in or on ribosomes. The inclusion RNA was resistant to RNase but could be removed by pepsin or potassium permanganate; it is probably in completed virus particles. Viral antigen was first observed in a perinuclear location and later in the above-mentioned inclusions. Although the viral protein contains appreciable amounts of arginine and lysine, it is not a basic protein of the histone type. Phase-contrast microscopy of living cells clearly demonstrated the role of the inclusions in release of virus from infected cells. A comparison is made between these cytological changes in Mengo-infected cells and those which have been found by other workers in polio-infected cells. There are many very similar changes.


1978 ◽  
Vol 30 (1) ◽  
pp. 99-115
Author(s):  
J. Bereiter-Hahn

Mitochondrial movements have been followed by phase-contrast microscopy in living XTH-cells (Xenopus laevis tadpole-heart cells) in tissue culture. The same organelles have been viewed subsequently in electron micrographs. Locomotion of mitochondria proceeds at velocities up to 100 micrometer/min. Formation of branches of mitochondria and other shape changes may occur with the same speed. Mitochondrial motility can be classified into 4 types: (I) Alternating extension and contraction at the two ends of rod-shaped mitochondria. (2) Lateral branching. (3) Alternate stretching and contraction of arbitrary parts of a mitochondrion amounting to a kind of peristaltic action. (4) Transverse wave propagation along the organelle. Types I to 3 can be reduced to the same underlying principle; they cause locomotion. Formation of mitochondrial extensions is due to elongation of cristae. The observations are discussed in terms of 4 specific proposals. (I) Intracellular locomotion of mitochondria is caused by local enlargements and contractions of the organelles. (2) The shape changes are correlated with alterations in the arrangement of the cristae. (3) Such arrangements are not associated with overall swelling or shrinkage of the mitochondrion; they are local features. (4) Estimates of the time required for rearrangement of the inner compartment amount to less than 0.3 s for single crista arrangements during the fastest shape changes, and less than 1–3 s during slower alterations. This high velocity is in good accord with the hypothesis of energy conservation by conformational events during oxidative phosphorylation.


1970 ◽  
Vol 20 (1) ◽  
pp. 63-67 ◽  
Author(s):  
T Sultana ◽  
T Sultana ◽  
MQ Rahman ◽  
ANN Ahmed

For centuries physicians have been using urine as one of the non-invasive means for assessing diseases. Haematuria is a frequently encountered abnormality in clinical practice. Haematuria may have either a glomerular or a non-glomerular origin. The morphological study of urinary red cells by Phase-Contrast Microscopy (PCM) is a useful diagnostic marker for glomerular bleeding, if correctly interpreted and used. Today, urinalysis and in particular identification of red cells morphology by Phase-Contrast Microscopy has been a widely accepted technique for determining the site of haematuria. A short review on haematuria and Phase-Contrast Microscopy are presented here for updating knowledge and academic interest. Key words: Phase-contrast microscope; Haematuria; Dysmorphic red cell. DOI: http://dx.doi.org/10.3329/jdmc.v20i1.8584 J Dhaka Med Coll. 2011; 20(1) :63-67


1981 ◽  
Author(s):  
K Tanoue ◽  
S M Jung ◽  
I Isohisa ◽  
C Sakakibara ◽  
S Ariga ◽  
...  

The relationship between aggregability and electrophoretic mobility (EPM) was studied to clarify the role of surface negative charge in platelet function. 1. Human platelets were washed 3 times with Phillip’s buffer (pH 7.4), resuspended to 107 platelets/ml in modified Zeiller and Hannig’s buffer with 1 mM EDTA and incubated with various concentrations of ADP, adrenaline, thrombin and ristocetin at 37°C for 3 min. Without further washing, mean EPM of about 700 platelets was determined by the automatic Laser Zee System 3000 with good reproducibility with less than 1 % variation coefficient for 5 measurements. In all experiments, aggregating agents were dissolved in physiologic saline to obtain the same solution conductance both in test and control platelet suspensions to which saline alone was added. Neither 1-100 uM ADP nor 5-500 μM adrenaline had any effect on platelet EPM. Thrombin decreased EPM with dose response relation with -1.692±0.014 μm/sec/V/cm without thrombin, -1.580±0.084 with o725 , -1.578±0.001 with 1.0, -1.454±0.018 with 2.0 and -1.289±0.004 with 5.0 U/ml of thrombin. Ristocetin had decreasing effect on EPM at 0.2 mg/ml or less. After addition of above aggregating agents, the washed platelets did not aggregate under phase contrast microscopy. 2. EPM of washed platelets were compared with aggregability in the PRP collected from 33 clinical cases with various degrees of aggregation. There was no correlation between EPM and secondary and maximum aggregation induced by any of these four agents. However, intensity of primary aggregation by adrenaline correlated with EPM (r= 0.485, P<0.01). The same tendency was observed in primary aggregation by ADP. 3. Treatment of washed rabbit platelets with increasing doses of neuraminidase resulted in increasing aggregation by ADP and collagen associated with decrease in EPM. These findings suggested that platelet surface negative charge may be regulatory role in initiation of platelet activation.


Author(s):  
Frank Smithson

Phase-contrast methods in microscopy appear to have been developed mainly with the intention of applying them to biological subjects, and their application to the examination of mineral substances has received only slight attention. Thin sections of rocks viewed under a phase-contrast microscope have a fascinatingly strange appearance and it does not take long to realize that some features are shown up more clearly and others less clearly than when viewed under an ordinary or a polarizing microscope. A considerable amount of work may be necessary before it is possible to assess the value of the new instrument for petrological purposes or to interpret all the phenomena observed by its aid. Nevertheless, it seems fitting to set out the following short account as a contribution towards this knowledge.


1979 ◽  
Author(s):  
H.K. Breddin ◽  
N. Bender ◽  
K. Kirchmaier ◽  
M. Ziemen

The sticking of platelets to basal membranes and to collagen fibers followed by subsequent aggregation are thought to be the first steps in hemostasis. During the first seconds after a vascular lesion platelets are stimulated outside the vessel and are transformed by forming pseudopodes and by sphering. Subcutaneous tissues of different species [human, Pig, dog, rat) as well as other tissues contain a lipoprotein with low tnrombo-plastic activity that stimulates platelets very rapidly. The action of this hemostasis activating factor (HaF) can be evaluated in fresh citrate blood by phase contrast microscopy and less specifically by the enhancement of platelet retention and the acceleration but not induction of platelet aggregation.HaF may play an important part in the activation of primary hemostasis. The proteins defective in v.-Willebrand’s syndrome are probably catalysing the stimulating effect of HaF on platelets. With new techniques the mechanism of the first steps in hemostasis can be further elucidated as well as the role of these mechanisms in thrombus formation.


1963 ◽  
Vol s3-104 (66) ◽  
pp. 185-191
Author(s):  
S. BRADBURY ◽  
G. A. MEEK

The acroblast of Helix spermatids is a duplex structure: it consists of an ‘externum’ (which appears dark by positive phase-contrast microscopy and becomes impregnated with osmium) enclosing a region called the ‘internum’. Histochemical studies show the externum to be composed principally of phospholipid and to contain glycolipid, alkaline phosphatase, and an enzyme which splits thiamine pyrophosphate. The internum contains neutral mucopolysaccharide. Ribonucleic acid and acid phosphatase are not present in the acroblast. These histochemical results suggest a homology between the invertebrate acroblast and the Golgi apparatus in vertebrate cells.


The stalks of peritrich protozoa have aroused great interest for many years and for many reasons. Some are contractile, some are not. This attribute of contractility, first observed by Leeuwenhoek in Vorticella and published in this journal in 1676, is one good reason for further studies of a structural, cytochemical and physiological character. This paper is mainly concerned with matters of fine structure which relate not only to the mechanism of contraction in those stalks that behave in this way, but also to wider problems of morphogenesis in ciliates. The early literature of this subject is clouded with optical artifact and one of the first problems to be solved is the precise difference between non-contractile and contractile stalks. Seven families are now included in the suborder Sessilina of the Peritrichida and members of the Epistylididae and the Vorticellidae have been selected for this investigation. This choice has made possible a detailed comparative study of fine structure in the non-contractile stalks of the first group and the contractile ones of the second. All stalks possess longitudinally arranged structures. In the non-contractile stalks these structures are tubular in form and may be observed in the phase-contrast microscope. In the contractile stalks the longitudinal structures are of two main kinds, one of which is confined to the annulus and the other to an inner canal separated from the annulus by a membrane. The annular structures are tubular and numerous in Carchesium and Zoothamnium and transversely striated, while in Vorticella they are composed of unstriated fibres, few in number. The structure within the canal is the main feature that distinguishes the stalks of Vorticellidae from those of Epistylididae. It consists of a long bundle of closely packed fine fibrils and is to be identified with the stalk spasmoneme or myoneme of the older literature. Only one type of fibril has been observed in the spasmonemes and present facts are not consistent with the idea that they contract in the same way as muscles. The spasmoneme is protein in nature with positive indications of the presence of —NH 2 , S—H, and S—S groups. The annular structure in the Vorticellidae and the tubular structures of Epistylididae have cytochemical affinities with the keratin group of proteins. Structurally, they grow out as the stalk develops from an assembly of organelles known collectively as the scopula. In the contractilia the spasmoneme passes into the zooid through a more or less central gap in the scopula and terminates in the form of a circular fan of fibrils on or close to the zooid pellicle. The fine structure of the stalk tubules of the Epistylididae has been investigated in some detail, particularly for one species of Epistylis. In Epistylis and Opercularia the tubules are transversely striated in a manner similar to that described for Carchesium and Zoothamnium . In Campanella each tubule consists of a loose helix of fibrils interlocked with those of neighbouring tubules. The form of attachment of the tubules of Epistylis and Opercularia to the scopula organelles has been determined. Wherever the preparations were of sufficient quality a comparison has been made of scopula organelles and the corresponding and possibly homologous structures of normal cilia known as basal bodies or kinetosomes. There are similarities and, of course, differences. It seems justifiable to regard the scopula organelles as basal bodies modified in the course of the evolution of this Order for the purpose of contributing a degree of structural stability and rigidity to the stalks. No such obvious ‘origin’ for the spasmoneme has been found in the adult organisms. This illustrates the danger and perhaps sterility of attempts to link the genesis of one structure to another on purely morphological grounds. The role of the scopula organelles and in a wider context kinetosomes in the organization and possibly the synthesis of fibrous proteins is discussed.


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