Functional changes with feeding in the gastro-intestinal epithelia of the Burmese python (Python molurus).

The morphology of the digestive system in fasting and refed Burmese pythons was determined, as well as the localization of the proton (H(+), K(+)-ATPase) and sodium (Na(+), K(+)-ATPase) pumps. In fasting pythons, oxyntopeptic cells located within the fundic glands are typically non-active, with a thick apical tubulovesicular system and numerous zymogen granules. They become active Immediately after feeding but return to a non-active state 3 days after the Ingestion of the prey. The proton pump, expressed throughout the different fasting/feeding states, is either sequestered in the tubulovesicular system in non-active cells or located along the apical digitations extending within the crypt lumen in active cells. The sodium pump is rapidly upregulated in fed animals and is classically located along the baso-lateral membranes of the gastric oxyntopeptic cells. In the Intestine, it is only expressed along the lateral membranes of the enterocytes, i.e., above the lateral spaces and not along the basal side of the cells. Thus, solute transport within the Intestinal lining is mainly achieved through the apical part of the cells and across the lateral spaces while absorbed fat massively crosses the entire height of the cells and flows into the Intercellular spaces. Therefore, in the Burmese python, the gastrointestinal cellular system quickly upregulates after feeding, due to Inexpensive cellular changes, passive mechanisms, and the progressive activation and synthesis of key enzymes such as the sodium pump. This cell plasticity also allows anticipation of the next fasting and feeding periods.

Cytokine expression in rat colon during postnatal development: regulation by glucocorticoids.

OBJECTIVES: Cytokine expression and regulation by glucocorticoids and retinoic acid were investigated in the colon during postnatal development. MATERIALS AND METHODS: Gene expression of the transforming growth factors (TGFs) TGF-beta1, TGF-beta2 and TGF-alpha and the proinflammatory cytokines tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) was evaluated by reverse transcription-polymerase chain reaction (RT-PCR) in rat colon mucosa during weaning and in adult rats. Protein expression and distribution of TGF-betas was analysed in the colon from 14- and 60-day-old animals. The effect of hydrocortisone administration on mucosal cytokine transcripts (RT-PCR) and of dexamethasone on the expression of cytokines by the epithelial cell line IEC-18 and 2 subepithelial myofibroblasts (MIC 307-1 and 316) was examined. RESULTS: TGF-beta1 and TGF-beta2 messenger RNAs and proteins decreased in the entire colon from weaning to adult stages, whereas the amount of TGF-alpha messenger RNA increased in the proximal colon and decreased in the distal part of the colon in adult rats in comparison with weanlings. However, proinflammatory cytokines showed no postnatal changes in the proximal colon but decreased in the distal part in comparison with weaning rats. Hydrocortisone treatment did not affect growth factor expression but decreased proinflammatory cytokines. Likewise, dexamethasone decreased TNF-alpha and IL-1beta gene expression but did not affect TGF-betas in either epithelial or myofibroblast cells. CONCLUSIONS: During postnatal maturation, the expression of growth factors and proinflammatory cytokines decreased in the distal colon, whereas in the proximal colon, a differential maturation occurs with no changes in proinflammatory cytokines, an increase in TGF-alpha and a decrease in TGF-beta. Glucocorticoids may control the developmental profile of proinflammatory cytokines.

Immunolocalization of Na+,K+-ATPase in the branchial cavity during the early development of the crayfish Astacus leptodactylus (Crustacea, Decapoda).

The ontogeny of osmoregulation was examined in the branchial cavity of embryonic and early post-embryonic stages of the crayfish Astacus leptodactylus maintained in freshwater, at the sub-cellular level through the detection of the sodium-potassium adenosine triphosphatase (Na(+),K(+)-ATPase). The embryonic rate of development was calculated according to the eye index (EI) which was 430-450 microm at hatching. The distribution of the enzyme was identified by immunofluorescence microscopy using a monoclonal antibody IgGalpha5 raised against the avian alpha-subunit of the Na(+),K(+)-ATPase. Immunoreactivity staining, indicating the presence of Na(+), K(+)-ATPase appeared in the gills of late embryos (EI>/=400 microm), i.e. a few days before hatching time, and steadily increased throughout the late embryonic and early post-embryonic development. The appearance of the enzyme correlates with the ability to osmoregulate which also occurs late in the embryonic development at EI 410-420 microm and with tissue differentiation within the gill filaments. These observations indicate that the physiological shift from osmoconforming embryos to hyper-regulating late embryos and post-hatching stages in freshwater must originate partly from the differentiation in the gill epithelia of ionocytes which are the site of ion pumping, as suggested by the location of Na(+),K(+)-ATPase. Only the gills were immunostained and a lack of specific staining was noted in the lamina and the branchiostegites. Therefore, osmoregulation through Na(+)active uptake is likely achieved in embryos at the gill level; all the newly formed gills in embryos function in ion regulation; other parts of the branchial chamber such as the branchiostegites and lamina do not appear to be involved in osmoregulation.