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In the pigeon (Columba livia), a different response of cutaneous water evaporation (CWE) is seen at different acclimation states. While in heat-acclimated pigeons the CWE at high ambient temperatures will be activated as expected, no such response to appropriate thermal stimuli is seen in cold-acclimated birds. This difference is also reflected in the function of the water barrier, which in the stratum corneum modulates the diffusion of water through the skin. In this respect, the skin of birds seems to be more dynamic than that of mammals. In mammals, the formation of this barrier by extracellular lipid lamellae derived from lamellar bodies of viable keratinocytes is a prerequisite for normal skin function. It is present in cold-acclimated pigeons, but is lacking in heat-acclimated birds. The ionic stimulus of extracellular calcium (Ca2+) has been claimed to mediate the formation of the mammalian-type barrier. In order to elucidate the role of Ca2+ in water barrier formation in avians, we studied winter-acclimatized and thermally non-challenged pigeons for their epidermal barrier structure and Ca2+ distribution by calcium capture cytochemistry by electron microscopy. In both groups of pigeons, we show that both the extracellular and the intracellular domains in the stratum corneum contain organized lamellar lipids. In the stratum corneum, the bulk Ca2+ is located in corneocytes. In thermally non-challenged birds, Ca2+ is localized also in the outer extracellular spaces.
We may conclude that, unlike in mammals, (1) corneocytes contain massive intracellular lamellae that extend up to the outer layers of the stratum corneum, and (2) Ca2+ accumulates in the corneocytes. This suggests that pigeons may lose substantial amounts of Ca2+ via desquamation and, on the other hand, the skin may serve as a Ca2+ reservoir. These results indicate a different role of Ca2+ in the water barrier formation, as well as novel functions of the avian skin as compared to that of mammals.
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Elias, P.M., Cullander, C., Mauro, T., Rassner, U., Kömüves, L., Brown, B., Menon, G.K. 1998a. The secretory granular cell: the outermost granular cell as a specialized secretory cell. J. Invest. Dermatol. Symp. Proc. 3: 87-100.
Haftek, M., Teillon, M-H., Schmitt, D. 1998. Stratum corneum, corneodesmosomes and ex vivo percutaneous penetration. Microsc. Res. Tech. 43: 242-249.
Menon, G.K., Grayson, S., Elias, P.M. 1985. Ionic calcium reservoirs in mammalian epidermis: ultrastructural localization by ion-capture cytochemistry. J. Invest. Dermatol. 84: 508-512.
Piersma,T., Gudmundsson, G.A., Davidson, N.C., Morrison, R.I.G. 1996. Do arctic-breeding Red Knots (Calidris canutus) accumulate skeletal calcium before egg laying? Can. J. Zool. 74: 2257-2261.
Peltonen, L., Arieli, Y., Harjula, R., Pyörnilä, A., Marder, J. 2000. Local cutaneous water barrier in cold- and heat-acclimated pigeons (Columba livia) in relation to cutaneous water evaporation. J. Morphol. 246: 118-130.
Arieli, Y., Feinstein, N., Raber, P., Horowitz, M., Marder, J. 1999. Heat stress induces ultrastructural changes in cutaneous capillary wall of heat-acclimated rock pigeon. Am. J. Physiol. 277: 967-974.
Carey, C. 1996. Female reproductive energetics. In: Carey, C., ed. Avian energetics and nutritional ecology. Chapman & Hall, New York, pp. 324-374.
Menon, G.K., Elias, P.M., Feingold, K.R. 1994a. Integrity of the permeability barrier is crucial for maintenance of the epidermal calcium gradient. Br. J. Dermatol. 130: 139-147.
Menon, G.K., Price, L.F., Bommannan, B., Elias, P.M., Feingold, K.R. 1994b. Selective obliteration of the epidermal calcium gradient leads to enhanced lamellar body secretion. J. Invest. Dermatol. 102: 789-795.
Mori, J.G., George, J.C. 1978. Seasonal changes in serum levels of certain metabolites, uric acid and calcium in the migratory Canada Goose (Branta canadensis interior). Comp. Biochem. Physiol. B 59: 263-269.
Pallon, J., Malmqvist, K.G., Werner-Linde, Y., Forslind, B. 1996. PIXE analysis of pathological skin with special reference to psoriasis and atopic dry skin. Cell. Mol. Biol. 42: 111-118.
Elias, P.M., Nau, P., Hanley, K., Cullander, C., Crumrine, D., Bench, G., Sidderas-Haddad, E., Mauro, T., Williams, M.L., Feingold, K.R. 1998b. Formation of the epidermal Ca gradient coincides with key milestones of barrier ontogenesis in the rodent. J. Invest. Dermatol. 110: 399-404.
Forlind, B., Werner-Linde, Y., Lindberg, M., Pallon, J. 1999. Elemental analysis mirrors epidermal differentiation. Acta Derm.-Venereol. (Stockh) 79: 12-19.
Graveland, J., Van Gijzen, T. 1994. Arthropods and seeds are not sufficient as calcium sources for shell formation and skeletal growth in passerines. Ardea 82: 299-314.
Jiang, S., Koo, S.-W., Lee, S.H. 1998. The morphologic changes in lamellar bodies and intercorneocyte lipids after tape stripping and occlusion with a water vapor-impermeable membrane. Arch. Dermatol. Res. 290: 145-151.
Lee, S.H., Choi, E.H., Feingold, K.R., Jiang, S., Ahn, S.K. 1998. Iontophoresis itself on hairless mouse skin induces the loss of the epidermal calcium gradient without skin barrier impairment. J. Invest. Dermatol. 111: 39-43.
Menon, G.K., Elias, P.M. 1997. Morphologic basis for a pore-pathway in mammalian stratum corneum. Skin Pharmacol. 10: 235-246.
Menon, G.K., Aggarwal, S.K., Lucas A.M. 1981. Evidence for the holocrine nature of lipoid secretion by avian epidermal cells: a histochemical and fine structural study of rictus and the uropygial gland. J. Morphol. 167: 185-199.
Ravazzolla, M. 1976. Intracellular localization of calcium in the chromaffin cells of the rat adrenal medulla. Endocrinology 98: 950-953.
Reynolds, E.S. 1963. The use of lead citrate at high pH as an electron opaque stain in electron microscopy. J. Cell Biol 17: 208-212.
Van den Bergh, B.A.I., Swartzendruber, D.C., Bos-Van der Geest, A., Hoogstraate, J.J., Schrijver, A.H.G.J., Boddé, H.E., Junginger, H.E., Bouwstra, J.A. 1997. Development of an optimal protocol for the ultrastructural examination of skin by transmission electron microscopy. J. Microsc. 187: 125-133.
Van der Meulen, J., Van den Bergh, B.A.I., Mulder, A.A., Mommaas, A.M., Bouwstra, J.A., Koerten, H.K. 1996. The use of vibratome sections for the ruthenium tetroxide protocol: a key for optimal visualization of epidermal lipid bilayers of the entire human stratum corneum in transmission electron microscopy. J. Microsc. 184: 67-70.
Vicanova, J., Boelsma, E., Mommaas, A.M., Kempenaar, J.A., Forslind, B., Pallon, J., Egelrud, T., Koerten, H.K., Ponec, M. 1998. Normalization of epidermal calcium distribution profile in reconstructed human epidermis is related to improvement of terminal differentiation and stratum corneum barrier formation. J. Invest. Dermatol. 111: 97-106.
| Insgesamt | Letzte 365 Tage | In den letzten 30 Tagen | |
|---|---|---|---|
| Aufrufe von Kurzbeschreibungen | 122 | 25 | 5 |
| Gesamttextansichten | 8 | 0 | 0 |
| PDF-Downloads | 8 | 0 | 0 |
In the pigeon (Columba livia), a different response of cutaneous water evaporation (CWE) is seen at different acclimation states. While in heat-acclimated pigeons the CWE at high ambient temperatures will be activated as expected, no such response to appropriate thermal stimuli is seen in cold-acclimated birds. This difference is also reflected in the function of the water barrier, which in the stratum corneum modulates the diffusion of water through the skin. In this respect, the skin of birds seems to be more dynamic than that of mammals. In mammals, the formation of this barrier by extracellular lipid lamellae derived from lamellar bodies of viable keratinocytes is a prerequisite for normal skin function. It is present in cold-acclimated pigeons, but is lacking in heat-acclimated birds. The ionic stimulus of extracellular calcium (Ca2+) has been claimed to mediate the formation of the mammalian-type barrier. In order to elucidate the role of Ca2+ in water barrier formation in avians, we studied winter-acclimatized and thermally non-challenged pigeons for their epidermal barrier structure and Ca2+ distribution by calcium capture cytochemistry by electron microscopy. In both groups of pigeons, we show that both the extracellular and the intracellular domains in the stratum corneum contain organized lamellar lipids. In the stratum corneum, the bulk Ca2+ is located in corneocytes. In thermally non-challenged birds, Ca2+ is localized also in the outer extracellular spaces.
We may conclude that, unlike in mammals, (1) corneocytes contain massive intracellular lamellae that extend up to the outer layers of the stratum corneum, and (2) Ca2+ accumulates in the corneocytes. This suggests that pigeons may lose substantial amounts of Ca2+ via desquamation and, on the other hand, the skin may serve as a Ca2+ reservoir. These results indicate a different role of Ca2+ in the water barrier formation, as well as novel functions of the avian skin as compared to that of mammals.
| Insgesamt | Letzte 365 Tage | In den letzten 30 Tagen | |
|---|---|---|---|
| Aufrufe von Kurzbeschreibungen | 122 | 25 | 5 |
| Gesamttextansichten | 8 | 0 | 0 |
| PDF-Downloads | 8 | 0 | 0 |