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1.
Biotech Histochem ; 88(5): 242-9, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23387424

ABSTRACT

The standard method for assessing blood cell characteristics using an ocular micrometer is time-consuming and limited. We used the Nikon NIS Elements imaging software and May- Grünwald-Giemsa staining to determine whether automated image analysis is suitable for rapid and accurate quantitative morphometry of erythrocytes. Blood was collected during four seasons from 126 geometric tortoises and the blood smears were evaluated for cell (C) and nuclear (N) characteristics of the erythrocytes. We measured area, length (L), width (W), perimeter, elongation and pixelation intensity, and calculated L/W and N/C areas. Erythrocyte size differed among cohorts; females, the larger sex, had smaller erythrocytes than either males or juveniles. Males had more elongated erythrocytes than females and erythrocytes of adults were more elongated than those of juveniles. Erythrocyte size and shape influence the efficiency of gas exchange owing to surface area to volume ratios, which are greater for small, elongated cells than for large, round cells. The high N/C ratio and low pixelation intensities of males and juveniles indicate that they may have had more immature erythrocytes in their circulation than females. The use of pixelation intensity to indicate the presence of immature erythrocytes was validated by seasonal differences that corresponded to the biology of the tortoises. Pixelation intensity was lowest in winter. We found that automated image analysis is a rapid and reliable method for determining cell size and shape, and it offers the potential for distinguishing among developmental stages that differ in staining intensity. The method should be useful for rapid health assessments, particularly of threatened species, and for comparative studies among different vertebrates.


Subject(s)
Erythrocytes/cytology , Image Processing, Computer-Assisted/methods , Protozoan Proteins/blood , Animals , Endangered Species , Female , Male , Sexual Maturation , Software , Staining and Labeling
2.
Brain Res Bull ; 70(4-6): 270-7, 2006 Oct 16.
Article in English | MEDLINE | ID: mdl-17027762

ABSTRACT

Previous studies have suggested that nocturnal and diurnal species of rodents differ in their circadian responses to light including phase shifts and early gene expression. Rhabdomys pumilio, the four-striped field mouse, is diurnal both in nature and in the laboratory. We studied in this species the response of the suprachiasmatic nucleus (SCN) to light stimuli at different time periods using light-induced expression of Fos as marker of neuronal activity. Fos induction in the SCN was investigated using immunohistochemistry and quantitative image analysis. The animals were exposed to a 15 min light pulse with monochromatic green light at different circadian times throughout a 24-h cycle. Animals maintained in constant darkness served as controls. R. pumilio exhibited an endogenous Fos rhythm in the SCN during constant darkness with highest expression during the subjective day at circadian time (CT) 2 and CT10. Photic stimulation resulted in significant Fos induction in the SCN at CT6, CT14, CT18 and CT22, compared to controls kept in constant darkness, with a peak of expression at CT22, i.e. during late subjective night, mainly due to expression in the ventral SCN. In tract tracing experiments based on the use of cholera toxin subunit B, we found that retinal fibres innervate mainly the contralateral ventral SCN. The intergeniculate leaflet received bilateral retinal innervation with overlap between ipsilateral and contralateral fibres. Altogether the data show that the rodent R. pumilio is a unique diurnal model for chronobiological studies.


Subject(s)
Gene Expression/radiation effects , Light , Oncogene Proteins v-fos/metabolism , Retina/physiology , Suprachiasmatic Nucleus/radiation effects , Animals , Circadian Rhythm/physiology , Functional Laterality/physiology , Immunohistochemistry/methods , Male , Mice , Photic Stimulation/methods , Retina/radiation effects , Time Factors , Visual Pathways/anatomy & histology , Visual Pathways/radiation effects
3.
J Clin Endocrinol Metab ; 86(5): 2243-9, 2001 May.
Article in English | MEDLINE | ID: mdl-11344234

ABSTRACT

The prevalence of cervical cancer in South African women is reported as being the highest in the world, occurring, on the average, in 60 of every 100,000 women. Cervical cancer is thus considered an important clinical problem in sub-Saharan AFRICA: Recent studies have suggested that epithelial tumors may be regulated by cyclooxygenase (COX) enzyme products. The purpose of this study was to determine whether cyclooxygenase-2 (COX-2) expression and PGE(2) synthesis are up-regulated in cervical cancers. Real-time quantitative RT-PCR and Western blot analysis confirmed COX-2 ribonucleic acid and protein expression in all cases of squamous cell carcinoma (n = 8) and adenocarcinoma (n = 2) investigated. In contrast, minimal expression of COX-2 was detected in histologically normal cervix (n = 5). Immunohistochemical analyses localized COX-2 expression and PGE(2) synthesis to neoplastic epithelial cells of all squamous cell (n = 10) and adenocarcinomas (n = 10) studied. Immunoreactive COX-2 and PGE(2) were also colocalized to endothelial cells lining the microvasculature. Minimal COX-2 and PGE(2) immunoreactivity were detected in normal cervix (n = 5). To establish whether PGE(2) has an autocrine/paracrine effect in cervical carcinomas, we investigated the expression of two subtypes of PGE(2) receptors, namely EP2 and EP4, by real-time quantitative RT-PCR. Expression of EP2 and EP4 receptors was significantly higher in carcinoma tissue (n = 8) than in histologically normal cervix (n = 5; P < 0.01). Finally, the functionality of the EP2/EP4 receptors was assessed by investigating cAMP generation after in vitro culture of cervical cancer biopsies and normal cervix in the presence or absence of 300 nmol/L PGE(2). cAMP production was detected in all carcinoma tissue after treatment with exogenous PGE(2) and was significantly higher in carcinoma tissue (n = 7) than in normal cervix (n = 5; P < 0.05). The fold induction of cAMP in response to PGE(2) was 51.1 +/- 12.3 in cervical carcinoma tissue compared with 5.8 +/- 2.74 in normal cervix. These results confirm that COX-2, EP2, and EP4 expression and PGE(2) synthesis are up-regulated in cervical cancer tissue and suggest that PGE(2) may regulate neoplastic cell function in cervical carcinoma in an autocrine/paracrine manner via the EP2/EP4 receptors.


Subject(s)
Adenocarcinoma/metabolism , Carcinoma, Squamous Cell/metabolism , Dinoprostone/biosynthesis , Gene Expression Regulation, Enzymologic , Isoenzymes/genetics , Prostaglandin-Endoperoxide Synthases/genetics , Receptors, Prostaglandin E/physiology , Uterine Cervical Neoplasms/metabolism , Cyclooxygenase 2 , Female , Humans , Membrane Proteins , Receptors, Prostaglandin E, EP2 Subtype , Receptors, Prostaglandin E, EP4 Subtype , Reverse Transcriptase Polymerase Chain Reaction , Up-Regulation
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