Cytological and Histological Study of Adult and Neonate Epidermis in Thick and Thin Skin of Various Anatomical Sites

2018 ◽  
Vol 9 (2) ◽  
Author(s):  
Hydar Muhsin Khalfa ◽  
Adnan Albideri ◽  
Haider Salih Jaffat
Keyword(s):  
Histological Study ◽  
Single Layer ◽  
Sweat Glands ◽  
Anatomical Site ◽  
Basal Cells ◽  
Histological Changes ◽  
Mature Adult ◽  
Skin Development ◽  
Stage Of Development ◽  
Thin Skin

The integumentary system covers the surface of the embryo (skin) and its specialized skin structures including hair, nails, sweat glands, mammary glands and teeth. During fetal skin development, the epidermis changes from a single layer of ectodermal cells at 7–8 days of gestation into a more apparent stratified, keratinized epithelium at 22–24 weeks. The aim of the study is to identify the histological and cytological changes that take place during neonatal and adult epidermis development. Human neonatal and adult samples were obtained from fully informed, consenting parent or releatives from Al-hilla mortary / Iraq. Neonatal samples were obtained from neonates after sudden deaths from maternity wards. Anatomical Sites included abdomen, forehead, back, shoulder and feet sole. A totoal of 15 neonates and 10 mature adults were used for this study. Fresh tissues were sectioned using a freezing cryostat. Tissues were sectioned at 5µm in -24°C and collected on microscopic slides. Slides were allowed to air dry for 30 min prior to hematoxyline and eosin staining. Tissues were also photographed using scanning electron microscopy SEM. Cytological measurements were taken using image j software and data was analysed using graph prism. Various cytological and histological changes takes place during neonatal and adult and epidermis development. Our study shows the stages of fair follicule formation as well as number of nucleated layers present at each stage of development and at different anatomical sites. Major histological changes takes places during the transition frm a neonate to a mature adult including the number of basal cells and epidermal thickness depending on the anatomical site.

scholarly journals Purinergic receptor detection in human embryonic epidermis

2018 ◽  
Vol 9 (SPL1) ◽  
Author(s):  
Hydar Muhsin Khalfa ◽  
Adnan Albideri ◽  
Haider Salih Jaffat
Keyword(s):  
Purinergic Receptors ◽  
Purinergic Receptor ◽  
Single Layer ◽  
Adenosine Diphosphate ◽  
High Rate ◽  
Sweat Glands ◽  
Purinergic Signalling ◽  
Stem Cell Markers ◽  
Skin Development ◽  
Proliferation And Differentiation

The integumentary system covers the surface of the embryo (skin) and its specialized skin structures including hair, nails, sweat glands, mammary glands and teeth. During fetal skin development, the epidermis changes from a single layer of ectodermal cells at 7–8 days of gestation into a more apparent stratified, keratinized epithelium at 22–24 weeks. Skin development is driven by the complex inter-play between intrinsic and extrinsic pathways. There has been significant interest in determining the molecular cues that regulate the proliferation of human epidermal cells.P2Y receptors are membrane bound G protein coupled receptors. Purinergic signalling mediated by nucleotides such as Adenosine Triphosphate (ATP) and Adenosine Diphosphate (ADP) has also been shown to play a significant role in embryogenesis. Aim:The aim of the study is to identify the presence of purinergic receptors P2Y1,P2Y2,and P2Y4 during human embryonic epidermis development. The expression of purinergic receptors is examined in various anatomical sites and embryonic stages. Human embryonic samples were obtained from fully informed,consenting patients undergoing spontaneous terminations of pregnancy from emergency department at Al-Hilla maternity. Anatomical Sites included abdomen,forehead,back and feet sole. A total of 15 embryos aged between 2-3 months were used for this study. Fresh tissues were sectioned using a freezing cryostat. Tissues were sectioned at 5µm in -24°C and collected on microscopic slides. Slides were allowed to air dry for 30 min prior to immunohistochemical processing. Our study shows strong positivestaining for purinergic receptors P2Y1,P2Y2,and P2Y4 in all selected anatomical sites. Immunohistochemical staining increases with gestational development in all selected anatomical sites. A strong expression of purinergic receptors is seen in anatomical areas which possess high rate of development and strong differentiation rate.purinergic receptors as stem cell markers are actively seen in human epidermis histogeneis and development. Their role is important is epidermal layer proliferation and differentiation.

Ultrastructure of the basal lamina of bovine ovarian follicles and its relationship to the membrana granulosa

Reproduction ◽  
2000 ◽  
pp. 221-228 ◽  
Author(s):  
HF Irving-Rodgers ◽  
RJ Rodgers
Keyword(s):  
Basal Lamina ◽  
Granulosa Cells ◽  
Light And Electron Microscopy ◽  
Single Layer ◽  
Antral Follicle ◽  
Basal Cells ◽  
Preantral Follicles ◽  
Antral Follicles ◽  
Cellular Processes ◽  
Innermost Layer

Different morphological phenotypes of follicular basal lamina and of membrana granulosa have been observed. Ten preantral follicles (< 0. 1 mm), and 17 healthy and six atretic antral follicles (0.5-12 mm in diameter) were processed for light and electron microscopy to investigate the relationship the between follicular basal lamina and membrana granulosa. Within each antral follicle, the shape of the basal cells of the membrana granulosa was uniform, and either rounded or columnar. There were equal proportions of follicles </= 4 mm in diameter with columnar basal cells and with rounded basal cells. Larger follicles had only rounded basal cells. Conventional basal laminae of a single layer adjacent to the basal granulosa cells were observed in healthy follicles at the preantral and antral stages. However, at the preantral stage, the conventional types of basal lamina were enlarged or even partially laminated. A second type of basal lamina, described as 'loopy', occurred in about half the preantral follicles and in half the antral follicles </= 4 mm diameter. 'Loopy' basal laminae were not observed in larger follicles. 'Loopy' basal laminae were composed of basal laminae aligning the basal surface of basal granulosa cells, but with additional layers or loops often branching from the innermost layer. Each loop was usually < 1 microm long and had vesicles (20-30 nm) attached to the inner aspect. Basal cellular processes were also common, and vesicles could be seen budding off from these processes. In antral follicles, conventional basal laminae occurred in follicles with rounded basal granulosa cells. Other follicles with columnar cells, and atretic follicles, had the 'loopy' basal lamina phenotype. Thus, follicles have different basal laminae that relate to the morphology of the membrana granulosa.

scholarly journals Experiments on skeletal growth and development in vitro in relation to the problem of avian phokomelia

1935 ◽  
Vol 118 (807) ◽  
pp. 133-154 ◽  
Keyword(s):  
Bone Formation ◽  
Bone Growth ◽  
Histological Study ◽  
Detailed Comparison ◽  
Specific Gene ◽  
Body Parts ◽  
Continue Development ◽  
Hatching Time ◽  
Stage Of Development

The experiments to be reported in the following pages were suggested by observations made by one of us on the so-called Creeper fowl. Creeper chickens are characterized by a disproportionate shortness of the long bones of the extremities. Histological study has shown that Creeper chickens belong in the same category as the disproportionate dwarfism of mammals known as chondrodystrophy or achondroplasia (Landauer, 1931) . The Creeper characters are inherited as a Mendelian dominant and are lethal in homozygous condition (Landauer and Dunn, 1930). Homozygous Creeper embryos generally die after about 72 hours of incubation, but in rare cases they survive beyond this stage and continue development up to nearly hatching time. These late stages of homozygous Creeper embryos exhibit striking malformations of the extremities which are known as phokomelia (Landauer, 1933). A study of the early embryonic development of homozygous Creeper embryos (Landauer, 1932) led to the conclusion that the effects of the Creeper mutation are not brought about by specific gene action on those body parts which later show deformities, but by a general retardation of body growth at a definite stage of development. This conclusion was strengthened by a detailed comparison of embryonic and post-natal bone growth in heterozygous Creeper and normal chickens (Landauer, 1934). All evidence which so far has been obtained in this work points to the conclusion that the characteristic traits of heterozygous as well as homozygous Creeper chicks are produced by an unspecific retardation of development at a time when formation of the buds of the extremities (and of the head which in homozygous embryos also shows deformities later on) are proceeding at a particularly rapid rate, thereby causing specific disturbances in the differentiation of these parts. It seemed to us that it should be possible to put these conclusions to an experimental test. The most promising way of approach appeared to be an attempt to produce in vitro the extreme abnormalities of bone formation shown by the extremities of phokomelic homozygous Creeper embryos. These abnormalities chiefly consist in (1) a general retardation of cartilage differentiation; (2) lack of bone formation; and (3) frequent partial fusion of ulna and radius on the one hand, tibia and fibula on the other, or presence of only one bone in these segments instead of two.

scholarly journals Anatomical and histological study of the kidneys and salt glands in great flamingos (Phoenicopterus roseus)

2016 ◽  
Vol 40 (1) ◽  
pp. 140-146
Author(s):  
Ali Faris Reshag
Keyword(s):  
Histological Study ◽  
Left Kidney ◽  
Relative Weight ◽  
Single Layer ◽  
Salt Gland ◽  
Total Body Weight ◽  
Peripheral Zone ◽  
Salt Glands ◽  
Connective Tissue Capsule ◽  
Collecting Ducts

     This study was designed to explain the anatomy and histology of kidneys and salt glands in Great Flamingos. Eight adult healthy Great Flamingos of both sexes have been used. The results showed that the kidneys in Great Flamingos consist of three separated lobes. The right kidney was longer 8.9±0.3 mm than the left kidney 8.4±0.4mm. The ratio of the kidneys weight to the total body weight was 0.39%. The salt gland was very large crescent shape, and occupied the supraorbital fossa and has 20.8±0.2mm long and 3.9±0.2mm in diameter. The volume of cortex was 60-70% and the medulla was 30-40%. Within the middle region of cortex there were numerous large corpuscles (mammalian type) and few of small corpuscles (reptilian type). There was a variation between the means diameters of mammalian type 59±1µm and reptilian type 42±0.9µm. The proximal and distal convoluted tubules and collecting ducts were lined by simple cuboidal epithelium and their means diameters were 46±0.9, 44±1 and 55.1±0.7µm, respectively. Within medulla the thick and thin segments were arranged at the peripheral zone of medullary cone while the collecting ducts were at the central part of cone and all were lined with simple cuboidal epithelium except thin segments were lined with squamous cells. The salt gland were consisted of lobules surrounded by thick connective tissue capsule and each has mass of branched tubuloacinar secretory unites. The latter were made up by single layer of cuboidal cells. The tubules lead into central duct lined by double layer of cuboidal cells while the main duct lined with stratified cuboidal epithelium. The secretory units of salt gland gave negative reaction to PAS and combined AB (pH 2.5) and PAS stains and this indicate the absence of neutral mucosubstances. The results concluded that the kidneys in great flamingo was small size organ with low relative weight in compare to birds size and the salt glands was active organ.

scholarly journals A study of histological changes of human placenta in rural population of eastern India

2018 ◽  
Vol 7 (8) ◽  
pp. 3280
Author(s):  
Mrinal Kanti Karmakar ◽  
Sambit Kar ◽  
S. M. Kumar ◽  
Subir Kumar Chattopadhyay ◽  
L. K. Vaid ◽  
...  
Keyword(s):  
Umbilical Cord ◽  
Cellular Proliferation ◽  
Histological Study ◽  
Normal Growth ◽  
Normal Pregnancy ◽  
Eastern India ◽  
Histological Changes ◽  
Endothelial Proliferation ◽  
Umbilical Cord Insertion ◽  
Normal Placenta

Background: Placenta is essential for maintenance of pregnancy and for promoting normal growth and development of fetus. It forms the morphological record of anatomical condition, intrauterine events and intrapartum events of gestation. Present study has been undertaken to record the data on the morphology and histology of placenta from mothers with hypertension and diabetes.Methods: This study showed several significant morphological and histological differences in the placenta of the mother with GDM and hypertensive placenta. The histological study of the placenta was done under microscope and number of syncytial knots, cytotrophoblastic cellular proliferation, fibrinoid necrosis, endothelial proliferation, calcified and hyalinised villous spots were noted per low power field in the diabetics and hypertensive group in comparison to control group.Results: All other parameters including area, thickness, diameter, and circumference of GDM placenta show a significant increase when compared with normal placenta. The gross anatomic features of placentae e.g infarcted areas, calcified areas and marginal insertion of the umbilical cord in the study group show significant increase in value (p>0.01) in diabetic and hypertensive groups when compared to that of the control or normal group.Conclusions: In present study we found that hypertensive placentae tend to be slightly smaller in size, weight, volume, area, thickness, diameter, circumference and feto-placental ratio than normal placentae but the parameters were found to be significantly greater than that of normal placentae in case of diabetic placentae. No significant differences were found in umbilical cord insertion. In normal pregnancy cases we found several histological findings which were increased in hypertensive and diabetic cases.

Histological changes in free jejunal grafts used in pharyngeal reconstruction

1991 ◽  
Vol 105 (7) ◽  
pp. 556-557 ◽  
Author(s):  
J. A. J. Deans ◽  
J. Hill ◽  
M. Bennett
Keyword(s):  
Inflammatory Infiltrate ◽  
Histological Study ◽  
Histological Changes ◽  
Free Grafts ◽  
Pharyngeal Reconstruction

AbstractA histological study was performed of biopsies taken from jejunal free grafts used in pharyngeal reconstruction. The main findings were a decreased crypt/villi ratio and a mild chronic inflammatory infiltrate. There was no evidence of metaplastic or dysplastic transformation.

Integrin expression during human epidermal development in vivo and in vitro

Development ◽  
1991 ◽  
Vol 112 (1) ◽  
pp. 193-206 ◽  
Author(s):  
M.D. Hertle ◽  
J.C. Adams ◽  
F.M. Watt
Keyword(s):  
Basement Membrane ◽  
Spatial Organization ◽  
Basal Layer ◽  
Subsequent Development ◽  
Sweat Glands ◽  
Collagen Type Iv ◽  
Integrin Expression ◽  
Basal Cells

In order to investigate the role of extracellular matrix receptors of the integrin family in establishing the spatial organization of epidermal kerotinocytes, we used immunofluorescence microscopy to examine the expression of a range of integrin subunits during development of human palm and sole skin. All of the integrins expressed during development were also present in mature epidermis and were largely confined to the basal layer of keratinocytes in a pericellular distribution. The alpha 3 and beta 1 subunits were expressed prior to the initiation of stratification and did not change in abundance or distribution during subsequent development. alpha 4 and beta 3 were not detected at any time in the epidermis. Every other subunit examined showed spatial or temporal changes in expression. Staining for alpha 1 was strong before stratification and until mid-development, but was greatly decreased in neonatal epidermis. alpha 2 was first detected in small patches of basal cells prior to stratification, and thereafter was found in the entire basal layer, with greater staining in developing sweat glands. alpha 5 was not expressed until mid-development, and then primarily in developing sweat glands, with faint expression in neonatal epidermis. alpha v was detected following stratification, in developing sweat glands, and occasionally in neonatal epidermis. alpha 6 and beta 4 were peribasally expressed before stratification, but thereafter became concentrated at the basal cell surface in contact with the basement membrane, co-localizing with hemidesmosomes as determined by staining with bullous pemphigoid antiserum. We also examined the distribution of three known ligands for keratinocyte integrins: laminin and collagen type IV were present in the basement membrane zone at all stages of development, whereas fibronectin was only evident there until about 13 weeks estimated gestational age. Finally, we found that the changes in integrin expression that occur on initiation of stratification in vivo could be reproduced in organ cultures of developing skin; such cultures therefore provided a useful experimental model for further studies of the role of integrins in epidermal stratification.

scholarly journals Influence of S(+)-ketamine analgesia in renal intraoperative ischemia: histological study in rats

2006 ◽  
Vol 21 (4) ◽  
pp. 242-246 ◽  
Author(s):  
Eloy Rusafa Neto ◽  
Pedro Thadeu Galvão Vianna ◽  
Rosa Marlene Viero ◽  
Norma Sueli Pinheiro Módolo ◽  
Eliana Marisa Ganem ◽  
...  
Keyword(s):  
Heart Rate ◽  
Arterial Pressure ◽  
Rectal Temperature ◽  
Wistar Rats ◽  
Histological Study ◽  
Sodium Pentobarbital ◽  
Histological Changes ◽  
Renal Histology ◽  
Male Wistar Rats ◽  
Arterial Hemorrhage

PURPOSE: To study in rats the effect of S(+)ketamine on the renal histology after intraoperative hemorrhage. METHODS: Twenty male Wistar rats, anesthetized with sodium pentobarbital, were randomly divided in 2 groups: G1 - control (n=l0) and G2 - S(+)-ketamine (n=10), both submitted to arterial hemorrhage of 30% of volemia in 3 moments (10% each 10 min) 60 min after anesthesia. G2 received S(+)-ketamine, 15 mg. kg-1, i.m., 5 min after anesthesia and 55 min before the 1st hemorrhage moment (Ml). Medium arterial pressure (MAP), rectal temperature (T) and heart rate were monitored. The animals were sacrificed in M4, 30 min after the 3rd hemorrhage moment (M3) and the kidneys and blood collected from hemorrhage were utilized for histological study and hematocrit (Ht) determination. RESULTS: There were significant reduction of MAP, T, and Ht. The histological study verified G1 = G2 for tubular dilation, congestion, and necrosis. The total score addition were significant1y different and G2 > G 1. CONCLUSION: Hemorrhage and hypotension determined changes in kidney histology. The rise in catecholamine blood concentration probably was the cause of S(+)-ketamine-induced higher score of histological changes.

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