Dinudom A, Komwatana P, Young J A, Cook D I
Department of Physiology, University of Sydney, New South Wales, Australia.
Am J Physiol. 1995 May;268(5 Pt 1):G806-12. doi: 10.1152/ajpgi.1995.268.5.G806.
We have previously shown that unstimulated granular duct cells of mouse mandibular gland contain a hyperpolarization-activated Cl- conductance with characteristics resembling the hyperpolarization-activated volume-sensitive Cl- channel (ClC-2). We now show that stimulation of these cells with forskolin, but not 1,9-dideoxyforskolin, activates a second whole cell Cl- conductance with properties resembling the cystic fibrosis transmembrane conductance regulator (CFTR). This conductance has a linear current-voltage relation and is not voltage activated. Its anion permeability sequence is Br- (1.96) > NO3- (1.36) > Cl- (1) > I- (0.44), and its conductance sequence is Cl- (1) > NO3- (0.66) > Br- (0.34) > I- (0.21). The current carried by this conductance is attenuated 65% by 1 mmol/l diphenylamine-2-carboxylate but is not affected by 0.1 mmol/l4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid or 0.1 mmol/l glibenclamide. The current can be activated by norepinephrine (1 mumol/l), evidently acting via beta-adrenergic receptors, since the effect of norepinephrine is inhibited by propranolol (1 mumol/l). We conclude that this adrenergically evoked conductance is due to CFTR, which has previously been shown to be expressed in salivary duct cells, and suggest that it may form part of the mechanism by which beta-adrenergic agonists modulate NaCl absorption by salivary ducts.
我们之前已经表明,小鼠下颌下腺未受刺激的颗粒导管细胞含有一种超极化激活的氯离子电导,其特性类似于超极化激活的容积敏感性氯离子通道(ClC-2)。我们现在表明,用毛喉素刺激这些细胞,而不是1,9-二脱氧毛喉素,可激活第二种全细胞氯离子电导,其特性类似于囊性纤维化跨膜电导调节因子(CFTR)。这种电导具有线性电流-电压关系,且不是电压激活的。其阴离子通透性顺序为Br-(1.96)>NO3-(1.36)>Cl-(1)>I-(0.44),其电导顺序为Cl-(1)>NO3-(0.66)>Br-(0.34)>I-(0.21)。这种电导所携带的电流被1 mmol/l二苯胺-2-羧酸盐衰减65%,但不受0.1 mmol/l 4,4'-二异硫氰酸根合芪-2,2'-二磺酸或0.1 mmol/l格列本脲的影响。该电流可被去甲肾上腺素(1 μmol/l)激活,显然是通过β-肾上腺素能受体起作用,因为去甲肾上腺素的作用被普萘洛尔(1 μmol/l)抑制。我们得出结论,这种肾上腺素能诱发的电导是由于CFTR,此前已证明其在唾液导管细胞中表达,并表明它可能构成β-肾上腺素能激动剂调节唾液导管对NaCl吸收机制的一部分。