The current study was designed to give a complete microscopic description of the ependymal cells of the one-humped camel (Camelus dromedarius) using histological, immunohistochemical, and transmission microscopic descriptions of the ependymal cells of the fresh 35 spinal cord samples immediately after their slaughtering. In our
The present investigation was prepared to describe the accessory sex glands of the Barki bucks grossly and by light microscopy. There are four sex glands: ampullary, vesicular, prostate, and bulbourethral. The ampullary gland is an enlargement of the terminal part of the ductus deferens, its glandular part has branched tubuloalveolar glands, and its secretory alveoli lined with a pseudo-stratified epithelium composed of cuboidal to columnar cells.The vesicular gland takes the appearance of a cluster of grapes and the left vesicular gland is enlarged and higher than the right one. The vesicular gland is a lobulated tubuloalveolar gland with wide intralobular space and the gland contain a secretory unit which lined by pseudo-stratified columnar epithelium, and the interlobular ductules lined by the stratified epithelium, while the interlobular duct lined by simple cuboidal epithelium moreover, the 2 lining epithelium of secretory part consists of tall columnar cells. The prostate gland consists only of the disseminated part and is enclosed by a connective tissue capsule that was thin dorsally, thick laterally, and reduced in thickness ventrally. The prostatic acini are lined by simple cuboidal epithelium. The bulbourethral gland was similar in size to the walnut and surrounded by a capsule and there are interlobular connective tissue septa that divided the gland into lobes and lobules of different sizes. The bulbourethral gland contains secretory units lined by the tall simple columnar epithelium of mucous type with basely located nuclei and eosinophilic cytoplasm contain granular secretion. The gross and microscopic examination of the four accessory sex glands gave valuable information in the future pathology diagnosis of the accessory sex glands of the Barki bucks.
Key words: Camel, BALT, Bronchus, BronchiolesThe BALT is an organized lymphoid tissue in the mucosa of the bronchi and bronchioles that samples antigens leading to lymphocytes stimulation. This vital structure was studied in different species but not in the camel. Therefore this work studied the bronchi and bronchioles of 14 healthy camels of different ages (10 months -12 years) using light and transmission electron microscope. BALT was regularly present in all specimens studied. It was variable in locations and structures. BALT was found in the form of patches across the circumference of the bronchial tree in the form of loose lymphocytic aggregations to a well-organized lymphoid tissue with secondary lymphoid follicles. It was localized in the lamina propria and sub mucosa or even the adventitia. At the margin of BALT, several high endothelial venules and lymphatics were localized. The BALT associated epithelium was formed from ordinary pseudo-stratified columnar ciliated epithelium with goblet cells in the bronchi and simple columnar in the bronchioles. Interepithelial lymphocytic infiltration of variable number was observed.
Buffaloes are essential part of the economy in many countries and provide sustainable food in addition to being working animals. Inefficiency in reproduction has become problematic in recent years due to a number of factors and although much research concentrates on the female, very little is known about the male buffalo reproductive system. To address this deficiency in the literature, testes were obtained from 20 clinically healthy water buffalo (Bubalus Bubalis) bulls aged 3 years old. Scanning electron microscopy showed that the Sertoli cells were columnar to triangle shaped with many processes. In the middle portion of the seminiferous tubules, the Sertoli cell had two types of processes with sheet like and slender cord like appearances. The sheet like processes had simple smooth margins originating from Sertoli cells, surrounding the surfaces of spermatogonia and spermatocytes. The slender cord like processes formed networks around other spermatogenic cells. Transmission electron microscopy showed that the Sertoli cells contained a large irregular shaped nucleus with deep nuclear membrane indentations, few mitochondria, aggregates of ribosomes and few rough endoplasmic reticulum which were observed within the indentations. Each nucleus contained a multivesicular nuclear body, containing vesicles, tubules and ribosome like dense structures. The work herein describes the structure and location of key reproductive cells within the water buffalo. Understanding the features of the male reproductive system is essential in order to advance studies into the reproductive decline of this species and the Bovidae family.
Thymus obtained from10 clinically healthy Egyptian water male buffalo (Bosbubalis
Key words: Catfish, Skin, Immunohistochemistry, SEM, TEM The current study aimed to explore the skin sructure at the larval and adult stages of the African catfish. Of the previous studies on the skin morphology of fish, none has researched the detailed skin differentiation at the larval and adult stages of the African catfish. Here by light microscopic investigation, the skin of the larva after hatching consisted of two layers of simple squamous epithelium. The skin of the 5-6 day old larva consisted of more than one layer of flattened to oval cells, continuous layer of melanocytes and club cells showed up. The skin of the 15-days old larva distinguished into epidermis, dermis and hypodermis. While the skin of the adult catfish, the epidermis consisted of three layers a basal layer of cuboidal or columnar cells, middle layer of polyhedral cells and surface layer of flattened cells. Its mucous cells were oval in shape having foamy cytoplasm. Its club cells had acidophilic cytoplasm and some cells were binucleated. At the lateral line, a group of elongated neuromasts viewed between the club cells. Langerhans like cell showed a positive reaction with CD 1a. The dermis divided into stratum spongiusm and stratum compactum. At lateral line beneath the hypodermis, the neuromast canal detected. By SEM, no any evidence of taste buds pores and neuromast detected at the newly hatched larva. Different forms of neuromast appeared on the surface as small epidermal protrusions at the 6-day old larva. In addition, the neuromast at the epidermal protrusion appeared with long and short hair bundles. While, the skin of the adult catfish, the surface epithelium showed many projections, the broken epidermis showed a large club cells, melanocytes with cytoplasmic processes and pores. By TEM of the adult catfish, the surface cells had (microridges), desmosomes distinguished between the neighboring epidermal surface cells. The club cells cytoplasm had scanty organelles, two types of club cells identified; the first type with no vesicular secretion and the second type with fibrillar cytoplasm. The plasma membrane showed many invaginations. The study recorded two types of neuromast; superficial neuromast and canal neuromast set in the dermis. No neurmast detected at the 1 st day larva afterthat it appeared and incresead in number and its shape changed from simillar hair cells to long and short hair bundles.
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