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   <subfield code="a">Localization of calcium in murine epidermis following disruption and repair of the permeability barrier</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Gopinathan Menon, Peter Elias, Seung Lee, Kenneth Feingold]</subfield>
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   <subfield code="a">Summary: Perturbation of the cutaneous permeability barrier results in rapid secretion of epidermal lamellar bodies, and synthesis and secretion of new lamellar bodies leading to barrier repair. Since external Ca2+ significantly impedes the repair response, we applied ion capture cytochemistry to localize Ca2+ in murine epidermis following barrier disruption. In controls, the numbers of Ca2+ precipitates in the basal layer were small, increasing suprabasally and reaching the highest density in the stratum granulosum. Barrier disruption with acetone produced an immediate, marked decrease in Ca2+ in the stratum granulosum, accompanied by secretion of lamellar bodies. Loss of this pattern of Ca2+ distribution was associated with the appearance of large Ca2+ aggregates within the intercellular spaces of the stratum corneum. The Ca2+-containing precipitates progressively reappeared in parallel with barrier recovery over 24 h. Disruption of the barrier with tape stripping also resulted in loss of Ca2+ from the nucleated layers of the epidermis, but small foci persisted where the stratum corneum was not removed; in these sites the Ca2+ distribution did not change and accelerated secretion of lamellar bodies was not observed. Following acetone-induced barrier disruption and immersion in isoosmolar sucrose, the epidermal Ca2+ gradient did not return, and both lamellar body secretion and barrier recovery occurred. However, with immersion in isoosmolar sucrose plus Ca2+, the epidermal Ca2+ reservoir was replenished, and both secretion of lamellar bodies and barrier recovery were impeded. These results demonstrate that barrier disruption results in loss of the epidermal Ca2+ reservoir, which may be the signal that initiates lamellar body secretion leading to barrier repair.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">Epidermis</subfield>
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   <subfield code="a">Permeability</subfield>
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   <subfield code="a">Calcium ions</subfield>
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   <subfield code="a">Ionic localization</subfield>
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   <subfield code="a">Mouse (hr/hr)</subfield>
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   <subfield code="u">Department of Dermatology and Medicine, University of California, San Francisco, California, USA</subfield>
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   <subfield code="t">Cell and Tissue Research</subfield>
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