1994
DOI: 10.1679/aohc.57.67
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Electron Microscopic Observation of the Transitional Portion in the Human Eccrine Sweat Gland.

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Cited by 3 publications
(4 citation statements)
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“…Anti-PCNA labelled a few secretory cells and outer cells of the duct, myoepithelial cells were not stained as in other eccrine glands [Morimoto and Saga, 1995]. In contrast to human eccrine glands, we could not find any highly proliferative germinative cells in the transitional portions or the coiled ducts [Hagiwara and Shibasaki, 1994], but the density of positively stained nuclei was higher in these parts if compared to the secretory compartments.…”
Section: Discussioncontrasting
confidence: 69%
“…Anti-PCNA labelled a few secretory cells and outer cells of the duct, myoepithelial cells were not stained as in other eccrine glands [Morimoto and Saga, 1995]. In contrast to human eccrine glands, we could not find any highly proliferative germinative cells in the transitional portions or the coiled ducts [Hagiwara and Shibasaki, 1994], but the density of positively stained nuclei was higher in these parts if compared to the secretory compartments.…”
Section: Discussioncontrasting
confidence: 69%
“…The transporters shown at the apical membrane of the inner layer and those at the basolateral membrane of the outer layer are those that have been reported in the literature: at the basolateral membrane are the Na ϩ /K ϩ -AT-Pase pump, localized at both cell layers (37), the chloride channel cystic fibrosis transport regulator (CFTR) (41), and a basolateral K ϩ channel (38,42); at the luminal membrane are the CFTR and the epithelial Na ϩ channel (ENaC) (10,38,44,46) and the vacuolar proton pump (V-ATPase) (11,18). As suggested by previous electron microscopy images (13,20), inner (luminal) and outer (peripheral) cell layers are represented as distinct, showing intercellular spaces between cells and gap junctions. This model differs from previous ones by incorporating the finding of the present study, showing the presence of NHE1 at the basolateral membrane of the outer layer (NHE1basal), at the lateral membrane of both cell layers (NHE1later), and at the junction between the inner and outer cell layers (NHE1inter).…”
Section: Chloride Involvement In Ph I Regulationmentioning
confidence: 73%
“…Given reabsorption rates of ϳ1 nl⅐ min Ϫ1 ⅐ mm Ϫ1 for the sweat duct (30) and an external diameter of 40 m (50), and estimating from the kidney the area of intercellular space per cm 2 of duct surface to be 0.004 (5,48), we obtain 3.33 ϫ 10 Ϫ3 cm/s for V. Next, with a value for epithelium thickness of 15 m (50), a tortuosity factor ␣ for the intercellular spaces, and an estimate of 10 Ϫ5 cm 2 /s for D, the EIPA diffusion coefficient, we obtain Jc /Jd ϭ 0.5␣. The intercellular spaces of the sweat duct are very tortuous (13,20), so ␣ and Jc /Jd must be much larger than 1. ing a concentration gradient of EIPA in these spaces. From this, it can be argued that the convective flux is very likely to reduce substantially the EIPA concentration in the intercellular spaces most remote from the basal side and therefore prevent full blockade of the exchangers in these area.…”
Section: Basolateral and Apical Membranes Of The Sweat Ductmentioning
confidence: 99%
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