Annulate lamellae in the Sertoli cells of guinea pig testis after unilateral torsion of the spermatic cord

1984 ◽  
Vol 42 ◽  
pp. 196-197
Author(s):  
J. Chakraborty ◽  
A. P. Sinha Hikim ◽  
J. S. Jhunjhunwala
Keyword(s):  
Sertoli Cells ◽  
Guinea Pigs ◽  
Spermatic Cord ◽  
Present Report ◽  
Cell Types ◽  
Annulate Lamellae ◽  
Spermatogenic Cells ◽  
Electron Microscopic ◽  
Structural Details ◽  
First Time

Although the presence of annulate lamellae was noted in many cell types, including the rat spermatogenic cells, this structure was never reported in the Sertoli cells of any rodent species. The present report is based on a part of our project on the effect of torsion of the spermatic cord to the contralateral testis. This paper describes for the first time, the fine structural details of the annulate lamellae in the Sertoli cells of damaged testis from guinea pigs.One side of the spermatic cord of each of six Hartly strain adult guinea pigs was surgically twisted (540°) under pentobarbital anesthesia (1). Four months after induction of torsion, animals were sacrificed, testes were excised and processed for the light and electron microscopic investigations. In the damaged testis, the majority of seminiferous tubule contained a layer of Sertoli cells with occasional spermatogonia (Fig. 1). Nuclei of these Sertoli cells were highly pleomorphic and contained small chromatinic clumps adjacent to the inner aspect of the nuclear envelope (Fig. 2).

scholarly journals Electron Microscopic Observations on Mitochondria of Rat Testes Fixed in Potassium Permanganate

1960 ◽  
Vol 7 (2) ◽  
pp. 311-314 ◽  
Author(s):  
William Zebrun ◽  
Hilton H. Mollenhauer
Keyword(s):  
Epithelial Cells ◽  
Potassium Permanganate ◽  
Apparent Density ◽  
Sertoli Cells ◽  
Structural Difference ◽  
Cell Types ◽  
Morphological Investigation ◽  
Spermatogenic Cells ◽  
Mitochondrial Membranes ◽  
Electron Microscopic

A morphological investigation of mitochondria within the seminal epithelial cells of rat testes fixed in potassium permanganate reveals differences in electron opacity between the internal mitochondrial membranes of spermatogenic cells and those of Sertoli cells. Some interpretations of the apparent density differences are briefly discussed. It is concluded that the different effects of permanganate fixation upon the mitochondria of these cell types may reflect a significant structural difference between them.

Spermatogenic cells and stages of the seminiferous epithelial cycle in the Indian gerbil field rat, Tatera indica

1994 ◽  
Vol 6 (6) ◽  
pp. 699 ◽  
Author(s):  
GS Bilaspuri ◽  
R Kaur
Keyword(s):  
Cell Types ◽  
Albino Rats ◽  
Spermatogenic Cells ◽  
Single Generation ◽  
Tatera Indica ◽  
Two Generations ◽  
Size And Morphology ◽  
Stage 1 ◽  
Different Cell Types ◽  
First Time

Four types of spermatogonia (A0, A, In, B) are distinguished in T. indica. Four generations of A type, a single generation of intermediate (In) and two generations of B type spermatogonia are identified. Seven divisions of spermatogonia have been observed, in Stages 1b, 2b, 3b, 4b, 5, 6 and 7 respectively. Spermatocytes have been observed in prophase, metaphase, anaphase and telophase; in terms of size and morphology, the phases of prophase could be further divided. Pre-leptotene and leptotene appear in Stage 8 and Stage 1 respectively. Round spermatids become asymmetrical in Stage 1b. For the first time in rodents, Stages 1, 2, 3, 4 and 8 have been subdivided. The percentage frequencies of Stages 1-8 are 12.93, 10.69, 17.54, 10.33, 3.76, 11.20, 7.88 and 25.67 respectively. Although the morphology of the spermatogenic cells and associations of these cell types are basically similar to those in albino rats, T. indica markedly differs from all other rodents studied in having two generations of B spermatogonia and subdivisions of Stages 1, 2, 3, 4 and 8; in addition, the relative frequencies of the stages distinctly differ from those recorded in previous studies of rats. Hence, the durations of different cell types in T. indica may differ markedly from those in other rodents.

scholarly journals Skeleton Growth in Guinea Pigs and Humans

2021 ◽  
Vol 9 ◽  
Author(s):  
Zoe Skinner ◽  
Natasha Clark ◽  
Sharon Rutland ◽  
Andrew Dawkins ◽  
Catrin Sian Rutland
Keyword(s):  
Computed Tomography ◽  
Guinea Pig ◽  
Guinea Pigs ◽  
Imaging Technique ◽  
Cell Types ◽  
Micro Computed Tomography ◽  
Internal Organs ◽  
Unique Structure ◽  
Different Ages ◽  
First Time

Every animal has a skeleton made up of many different bones. Bones are vital. Without bones we would not be able to move, protect our internal organs, store important minerals, or even make some cell types! When we are young, in addition to growing, our bones must develop into specific shapes. This article describes how and why bones grow and heal in humans and guinea pigs. Using a special imaging technique called micro-computed tomography, we will show you the unique structure of some guinea pig bones and how animals of different ages have important bone variations. We will also discuss how the fascinating discovery of a hole in a bone, called a supratrochlear foramen, was described for the first time in a species. We will also answer questions, such as “how can you keep your bones healthy” and “what happens to astronauts’ skeletons in space?”

An electron microscopic study of the formation and structure of the periostracum in Astarte (Bivalvia)

1974 ◽  
Vol 52 (12) ◽  
pp. 1463-1471 ◽  
Author(s):  
A. S. M. Saleuddin
Keyword(s):  
Microscopic Study ◽  
Electron Microscopic Study ◽  
Cell Types ◽  
Homogeneous Layer ◽  
Fibrous Layer ◽  
Electron Microscopic ◽  
The Third ◽  
Thin Sectioning ◽  
Structural Details ◽  
Different Cell Types

An electron microscopic study of the outer and middle folds of the mantle edge of Astarte castanea reveals the fine-structural details of the cells which are involved in the formation of the periostracum. There are four types of cells in the outer fold whereas there is only one type in the middle fold. The role of different cell types in the formation of the periostracum has been discussed. The periostracum originates in the intercellular space between the basal cell of the outer fold and the first cell of the middle fold. Even at the point of origin it consists of two outer membranous layers and the inner dark homogeneous layer. The fibrous translucent layer, which is the third layer of the fully mature periostracum, does not appear until the young periostracum has moved down the periostracal groove at the level of the third cell. As the periostracum matures, the two membranous layers remain remarkably constant in width, whereas the two inner layers, dark homogeneous and fibrous translucent, increase in thickness. Scanning electron microscopy and thin sectioning reveal that the fully mature periostraca of A. castanea and A. elliptica appear uniformly pitted, but the nature of the pits between the two species is different. The fibrils of the fibrous layer show either uniform or random arrangements, depending on the region. It is the innermost part of the fibrous layer of the periostracum that provides the nuclei for calcification.

scholarly journals Spermatogenic cells of the prepuberal mouse: isolation and morphological characterization

1977 ◽  
Vol 74 (1) ◽  
pp. 68-85 ◽  
Author(s):  
AR Bellve ◽  
JC Cavicchia ◽  
CF Millette ◽  
DA O'Brien ◽  
YM Bhatnagar ◽  
...  
Keyword(s):  
Sertoli Cells ◽  
Morphological Characteristics ◽  
Type A ◽  
Cell Types ◽  
Specific Cell ◽  
Spermatogenic Cells ◽  
Type B ◽  
Primitive Type ◽  
Pachytene Spermatocytes ◽  
Type A Spermatogonia

A procedure is described which permits the isolation from the prepuberal mouse testis of highly purified populations of primitive type A spermatogonia, type A spermatogonia, type B spermatogonia, preleptotene primary spermatocytes, leptotene and zygotene primary spermatocytes, pachytene primary spermatocytes and Sertoli cells. The successful isolation of these prepuberal cell types was accomplished by: (a) defining distinctive morphological characteristics of the cells, (b) determining the temporal appearance of spermatogenic cells during prepuberal development, (c) isolating purified seminiferous cords, after dissociation of the testis with collagenase, (d) separating the trypsin-dispersed seminiferous cells by sedimentation velocity at unit gravity, and (e) assessing the identity and purity of the isolated cell types by microscopy. The seminiferous epithelium from day 6 animals contains only primitive type A spermatogonia and Sertoli cells. Type A and type B spermatogonia are present by day 8. At day 10, meiotic prophase is initiated, with the germ cells reaching the early and late pachytene stages by 14 and 18, respectively. Secondary spermatocytes and haploid spermatids appear throughout this developmental period. The purity and optimum day for the recovery of specific cell types are as follows: day 6, Sertoli cells (purity>99 percent) and primitive type A spermatogonia (90 percent); day 8, type A spermatogonia (91 percent) and type B spermatogonia (76 percent); day 18, preleptotene spermatocytes (93 percent), leptotene/zygotene spermatocytes (52 percent), and pachytene spermatocytes (89 percent), leptotene/zygotene spermatocytes (52 percent), and pachytene spermatocytes (89 percent).

scholarly journals PSXIII-5 The age dynamics of the spermatogenic cells development in the roosters’ testes

2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 373-373
Author(s):  
Anastasia N Vetokh ◽  
Natalia A Volkova ◽  
Evgeniya K Tomgorova ◽  
Ludmila A Volkova ◽  
Natalia A Zinovieva
Keyword(s):  
Germ Cells ◽  
Sertoli Cells ◽  
Genetic Material ◽  
Cell Types ◽  
Seminiferous Tubules ◽  
Sperm Cells ◽  
Spermatogenic Cells ◽  
Different Cell Types ◽  
Hematoxylin Eosin ◽  
Testis Tissue

Abstract The cells of the male gonads are considered as a valuable genetic material for the conservation of the gene pool of breeds and lines of agricultural birds, as well as the directed modification of the poultry genome. Mature germ cells – spermatozoa and their predecessors – spermatogonia, spermatocytes and spermatids can be used for these purposes. To obtain these types of cells, it is necessary to know the characteristics of their development (spermatogenesis). The dynamics of the development of certain spermatogenic cell types in the testicular tubules of different-aged roosters has been studied. Histological studies were performed on testes of roosters aged from 1 week to 6 months with an interval of 2 weeks. Samples of testis tissue were fixed in Bouin’s solution. Histological sections were stained with hematoxylin-eosin. Identification of different cell types (Sertoli, spermatogonia, spermatocytes, spermatids, sperm cells) was carried out according to their morphology. At the age of 1–6 weeks in the seminiferous tubule of roosters, the mainly presence of two cell types was noted: Sertoli cells and spermatogonia. From 7 weeks of age, spermatocytes were detected in the seminiferous tubules, in the 4 months - spermatids, in the 5.5 months - sperm cells. The number of Sertoli cells remained almost unchanged with age and was 21 ± 2. The percentage of these cells decreased with age from 71 ± 3 % to 5 ± 1 %. The percentage of spermatogonia also decreased with age from 75 ± 2 % to 7 ± 1 %. The number of spermatids and spermatozoa, on the contrary, increased to puberty (6 months) and reached 54 %. The study was supported by the RFBR within Project no.18-29-07079.

The Morphology of the Rat Kidney Following Folic Acid Administration

1970 ◽  
Vol 28 ◽  
pp. 200-201
Author(s):  
Aline Byrnes ◽  
Elsa E. Ramos ◽  
Minoru Suzuki ◽  
E.D. Mayfield
Keyword(s):  
Folic Acid ◽  
De Novo ◽  
Specific Activity ◽  
Rat Kidney ◽  
Present Report ◽  
Intracellular Localization ◽  
Male Rats ◽  
Renal Hypertrophy ◽  
Electron Microscopic ◽  
Biochemical Alterations

Renal hypertrophy was induced in 100 g male rats by the injection of 250 mg folic acid (FA) dissolved in 0.3 M NaHCO3/kg body weight (i.v.). Preliminary studies of the biochemical alterations in ribonucleic acid (RNA) metabolism of the renal tissue have been reported recently (1). They are: RNA content and concentration, orotic acid-c14 incorporation into RNA and acid soluble nucleotide pool, intracellular localization of the newly synthesized RNA, and the specific activity of enzymes of the de novo pyrimidine biosynthesis pathway. The present report describes the light and electron microscopic observations in these animals. For light microscopy, kidney slices were fixed in formalin, embedded, sectioned, and stained with H & E and PAS.

Dendritic cells of the human epidermis: immuno-electron microscopic studies of la antigen reactivity

1978 ◽  
Vol 36 (2) ◽  
pp. 644-645
Author(s):  
G. Rowden ◽  
M. G. Lewis ◽  
T. M. Phillips
Keyword(s):  
Dendritic Cells ◽  
Langerhans Cells ◽  
Cell Types ◽  
Cell Type ◽  
Electron Microscopic ◽  
La Antigen ◽  
Microscopic Studies ◽  
A Cell ◽  
C3 Receptors ◽  
Antigen Reactivity

Langerhans cells of mammalian stratified squamous epithelial have proven to be an enigma since their discovery in 1868. These dendritic suprabasal cells have been considered as related to melanocytes either as effete cells, or as post divisional products. Although grafting experiments seemed to demonstrate the independence of the cell types, much confusion still exists. The presence in the epidermis of a cell type with morphological features seemingly shared by melanocytes and Langerhans cells has been especially troublesome. This so called "indeterminate", or " -dendritic cell" lacks both Langerhans cells granules and melanosomes, yet it is clearly not a keratinocyte. Suggestions have been made that it is related to either Langerhans cells or melanocyte. Recent studies have unequivocally demonstrated that Langerhans cells are independent cells with immune function. They display Fc and C3 receptors on their surface as well as la (immune region associated) antigens.

A microscopic marker experiment study on high temperature oxidation of Ni-Al alloy

1986 ◽  
Vol 44 ◽  
pp. 514-515
Author(s):  
Shou-kong Fan
Keyword(s):  
Transport Mechanism ◽  
High Temperature Oxidation ◽  
Transverse Section ◽  
Al Alloy ◽  
Metal Interface ◽  
Electron Microscopic ◽  
Temperature Oxidation ◽  
Analytical Electron ◽  
Microscopic Studies ◽  
First Time

Transmission and analytical electron microscopic studies of scale microstructures and microscopic marker experiments have been carried out in order to determine the transport mechanism in the oxidation of Ni-Al alloy. According to the classical theory, the oxidation of nickel takes place by transport of Ni cations across the scale forming new oxide at the scale/gas interface. Any markers deposited on the Ni surface are expected to remain at the scale/metal interface after oxidation. This investigation using TEM transverse section techniques and deposited microscopic markers shows a different result,which indicates that a considerable amount of oxygen was transported inward. This is the first time that such fine-scale markers have been coupled with high resolution characterization instruments such as TEM/STEM to provide detailed information about evolution of oxide scale microstructure.

Correlative transmission and high-resolution scanning electron microscopic studies on pituitary cells

1990 ◽  
Vol 48 (3) ◽  
pp. 20-21
Author(s):  
S. Tai
Keyword(s):  
Cell Types ◽  
Depth Of Field ◽  
Secretory Cells ◽  
Specific Cell ◽  
Pituitary Cells ◽  
Electron Microscopic ◽  
3 Dimensional ◽  
Microscopic Studies ◽  
Structure And Activity ◽  
Intracellular Structure

Extensive cytological and histological research, correlated with physiological experimental analysis, have been done on the anterior pituitaries of many different vertebrates which have provided the knowledge to create the concept that specific cell types synthesize, store and release their specific hormones. These hormones are stored in or associated with granules. Nevertheless, there are still many doubts - that need further studies, specially on the ultrastructure and physiology of these endocrine cells during the process of synthesis, transport and secretion, whereas some new methods may provide the information about the intracellular structure and activity in detail.In the present work, ultrastructural study of the hormone-secretory cells of chicken pituitaries have been done by using TEM as well as HR-SEM, to correlate the informations obtained from 2-dimensional TEM micrography with the 3-dimensional SEM topographic images, which have a continous surface with larger depth of field that - offers the adventage to interpretate some intracellular structures which were not possible to see using TEM.

Sign in / Sign up

Export Citation Format

Share Document