ライフサイエンスコーパス: chromaffin cell

1 ic vesicle, and a medium size vesicle in the chromaffin cell.

2 wo sequential priming steps in mouse adrenal chromaffin cells.

3 e nerve and form postsynaptic neuroendocrine chromaffin cells.

4 iated fusion pore expansion in mouse adrenal chromaffin cells.

5 ippocampus, dorsal root ganglia, and adrenal chromaffin cells.

6 ventional active zones and in neuroendocrine chromaffin cells.

7 augmented T-type Ca2+ current in IH-treated chromaffin cells.

8 correlation, confirming similar findings in chromaffin cells.

9 stimulated catecholamine release in cultured chromaffin cells.

10 spatial distribution of calcium channels in chromaffin cells.

11 d released by exocytosis in PC12 and primary chromaffin cells.

12 adapted from a model for fast exocytosis in chromaffin cells.

13 typical transmitter storage and release from chromaffin cells.

14 nd neuronal cells, including sympathoadrenal chromaffin cells.

15 on with a D1-like receptor on bovine adrenal chromaffin cells.

16 omosyn-syntaxin 1A complexes in live adrenal chromaffin cells.

17 type/reporter plasmids were transfected into chromaffin cells.

18 receptors on exocytosis from bovine adrenal chromaffin cells.

19 se frequency of catecholamine in dissociated chromaffin cells.

20 ant (>90%) mode of secretion in calf adrenal chromaffin cells.

21 calcium-triggered catecholamine release from chromaffin cells.

22 Ca) was produced by P2Y receptors in adrenal chromaffin cells.

23 motions related to the secretory response in chromaffin cells.

24 le priming and secretory amplitude in living chromaffin cells.

25 e in the Ca2+-cooperativity of exocytosis in chromaffin cells.

26 ficant reduction in DCG formation in adrenal chromaffin cells.

27 human embryonic kidney HEK293-S3 and adrenal chromaffin cells.

28 is a rare, but clinically important tumor of chromaffin cells.

29 18-1/syntaxin1A interaction in HEK293-S3 and chromaffin cells.

30 ive anion equilibrium potential, depolarizes chromaffin cells.

31 coupling after this peptidergic stimulus to chromaffin cells.

32 1-L61) were transiently expressed in adrenal chromaffin cells.

33 secretory response triggered by the toxin in chromaffin cells.

34 athetic neurons appears to represent adrenal chromaffin cells.

35 K"- or "Maxi K"-encoding Slo gene in adrenal chromaffin cells.

36 synapses as well as secretory cells, such as chromaffin cells.

37 d," was confirmed by immunohistochemistry at chromaffin cells.

38 in the exocytotic membrane fusion process in chromaffin cells.

39 ranscriptional activation of the VIP gene in chromaffin cells.

40 ease and extrusion from vesicles at mast and chromaffin cells.

41 ar calcium release, and elevation of cAMP in chromaffin cells.

42 ht to mediate BK channel inactivation in rat chromaffin cells.

43 ion is severely inhibited in Ophn1 knock-out chromaffin cells.

44 SPNs), respectively, from adrenal medullary chromaffin cells.

45 ind Rab3a-GTP and to stimulate exocytosis in chromaffin cells.

46 ar the plasma membrane (PM) of living bovine chromaffin cells.

47 ed action potentials (sAP) in bovine adrenal chromaffin cells.

48 properties of epinephrine-secreting adrenal chromaffin cells.

49 nist-induced hGH release from bovine adrenal chromaffin cells.

50 n the exocytotic membrane fusion reaction in chromaffin cells.

51 ease from the regulated secretory pathway in chromaffin cells.

52 ilar time course in AtT-20, CHO, and adrenal chromaffin cells.

53 ecretion observed in digitonin-permeabilized chromaffin cells.

54 was observed in native channels from bovine chromaffin cells.

55 hn1 knock-out mice and OPHN1-silenced bovine chromaffin cells.

56 ipid microdomains at the exocytotic sites in chromaffin cells.

57 he nAChR subtypes expressed by human adrenal chromaffin cells.

58 and is also essential for vesicle docking in chromaffin cells.

59 med during catecholamine exocytosis in mouse chromaffin cells.

60 nk exocytosis to compensatory endocytosis in chromaffin cells.

61 nergic stimulated catecholamine release from chromaffin cells.

62 duced bulk endocytosis also occurs in bovine chromaffin cells.

63 tivator (tPA) (over many seconds) in adrenal chromaffin cells.

64 large, dense core vesicles (LDCVs) in mouse chromaffin cells.

65 uptake at the synaptic terminals and adrenal chromaffin cells.

66 mice, we find that NPY is synthesized by all chromaffin cells.

67 es in a millisecond time resolution in mouse chromaffin cells.

68 successfully from multiple individual living chromaffin cells.

69 AP-25 x synaptotagmin-1 interaction in mouse chromaffin cells.

70 iNW-FET) to detect the K(+)-efflux from live chromaffin cells.

71 holamines released from small populations of chromaffin cells.

72 echolamines, exclusively, from fetal adrenal chromaffin cells.

73 Adrenal chromaffin cells (ACCs), stimulated by the splanchnic ne

74 e changes in the surface membrane of adrenal chromaffin cells after stimulation of exocytosis with a

75 e via desensitization/down-regulation of the chromaffin cell alpha(2)-adrenergic receptors that norma

76 n of neural crest-derived catecholaminergic (chromaffin) cells already associated with blood vessels

77 Ganglion neurons and adrenal chromaffin cells also show strong expressions.

78 In addition to the catecholamines, chromaffin cells also synthesize a range of peptides, in

79 onitoring of exocytotic events from cultured chromaffin cells and adrenal slices.

80 in the purified large dense-core vesicles of chromaffin cells and associated with synaptotagmin-1.

81 an directly affect the secretory capacity of chromaffin cells and contribute, in part, to elevated ca

82 nsmission on sympathetic neurons and adrenal chromaffin cells and elevates cytosolic ROS.

83 the internal pH of the secretory vesicles of chromaffin cells and enteric neurons.

84 and vesicular catecholamine transporters of chromaffin cells and facilitates localization of the pri

85 investigated this question in mouse adrenal chromaffin cells and found that SNAP-25 inhibits Ca(2+)

86 nergic receptors are found on bovine adrenal chromaffin cells and have been implicated in the facilit

87 (APWs) using both native channels in adrenal chromaffin cells and heterologously expressed channels i

88 irst study of EP receptor signaling in mouse chromaffin cells and identifies a molecular mechanism fo

89 s, in vesicle docking and secretion in mouse chromaffin cells and in cell-free assays.

90 tory capacity measured amperometrically from chromaffin cells and in the expression of tyrosine hydro

91 nd [Ca2+]i responses in neonatal rat adrenal chromaffin cells and involves reactive oxygen species (R

92 Using adrenal chromaffin cells and neurons, we now find that both over

93 th catecholamines from secretory vesicles in chromaffin cells and noradrenergic neurons.

94 repinephrine released from adrenal medullary chromaffin cells and norepinephrine released locally fro

95 mega-shaped structure in live neuroendocrine chromaffin cells and pancreatic beta-cells, visualized u

96 and histamine H(1) receptor in mouse adrenal chromaffin cells and PC12 cells.

97 ibitor of catecholamine release from adrenal chromaffin cells and postganglionic sympathetic axons.

98 protein released from secretory granules of chromaffin cells and sympathetic nerves, triggers endoth

99 entiation and increased apoptosis in adrenal chromaffin cells and sympathetic neurons.

100 hrough voltage-gated Ca2+ channels in bovine chromaffin cells and the domain of this receptor variant

101 n the development of sympathetic neurons and chromaffin cells and the mechanisms involved in Lin28B-i

102 proximity to the surface of adherent bovine chromaffin cells and to amperometrically record single e

103 (TH) in catecholamine-producing neurons and chromaffin cells and tyrosinase in melanocytes.

104 at controls epinephrine release from adrenal chromaffin cells and, consequently, hepatic glucose prod

105 that is found in neurons, platelets, adrenal chromaffin cells, and a few other neurosecretory cells.

106 epinephrine is released from adrenomedullary chromaffin cells, and compensatory glucogenesis ensues.

107 ed transcriptional mechanisms in transfected chromaffin cells, and concluded with observations on blo

108 n of individual secretory granules in living chromaffin cells, and related their mobilities to postfu

109 , is preferentially phosphorylated in intact chromaffin cells, and the levels of annexin 7 phosphoryl

110 Adrenal chromaffin cells are an important part of the neuroendoc

111 Adrenal medullary chromaffin cells are innervated by the sympathetic splan

112 Chromaffin cells are known to express functional GABA(A)

113 onclude that sympathetic neurons and adrenal chromaffin cells are more vulnerable to diabetes than pa

114 findings demonstrate that the fetal adrenal chromaffin cells are the source for acute hypoxaemia-ind

115 We demonstrate that large numbers of chromaffin cells arise from peripheral glial stem cells,

116 ecretory vesicles (chromaffin granules) from chromaffin cells as a glycoprotein of 72-73 kDa.

117 d catestatin is secreted from neuroendocrine chromaffin cells as an autocrine regulator of nicotine-s

118 hromocytoma cells and bovine adrenomedullary chromaffin cells as detected by Northern blotting, Weste

119 acitance measurements to probe exocytosis in chromaffin cells at low concentrations of intracellular

120 When secretion was measured from chromaffin cells, brief depolarizations triggered peptid

121 ion did not evoke action potential firing in chromaffin cells but did cause a persistent subthreshold

122 brane area through exocytosis does not swell chromaffin cells but may decrease membrane tension.

123 nt from mature secretory vesicles in adrenal chromaffin cells, but localizes to a compartment near th

124 ls (a rat insulinoma cell line) and cultured chromaffin cells, but not in AtT-20 cells (derived from

125 ediating SNARE-dependent exocytosis in mouse chromaffin cells, but the role of a closely related calc

126 or monitoring single vesicle exocytosis from chromaffin cells by constant potential amperometry as we

127 alin in secretory vesicles of neuroendocrine chromaffin cells by immunofluorescent confocal and immun

128 sponse element motif, an effect confirmed in chromaffin cells by site-directed mutagenesis on the tra

129 These results show that chromaffin cells can respond to depolarizing stimuli wit

130 ssociated with the effects of CIH on adrenal chromaffin cell catecholamine secretion.

131 Direct nicotinic stimulation of chromaffin cells caused catecholamine release and transg

132 e was measured from bovine adrenal medullary chromaffin cell (CC) cultures maintained over a period o

133 In chromaffin cells, CHGA and KLKB1 proteins co-localized i

134 In this study we demonstrate that chromaffin cells contain a protein antigenically similar

135 o shrink the Omega-profile in neuroendocrine chromaffin cells containing approximately 300 nm vesicle

136 are increased by Sp and that elevate 5-HT in chromaffin cell cultures, suggesting direct metabolic si

137 describes the primary culture of individual chromaffin cells derived by enzymatic digestion from the

138 We used amperometric recordings from chromaffin cells derived from mice that overexpress A30P

139 of NGF signaling for sympathetic neural and chromaffin cell development.

140 l sympathetic neuroblast hyperplasia, blocks chromaffin cell differentiation, and ultimately triggers

141 evoked secretion simultaneously from several chromaffin cells directly cultured on the device surface

142 owever, unlike hypothalamic nerve terminals, chromaffin cells do not display syntilla activation by d

143 synapses lacking Munc13s, the corresponding chromaffin cells do not exhibit a vesicle docking defect

144 surface membrane while secretory granules in chromaffin cells do not.

145 techolamine biosynthetic capacity of adrenal chromaffin cells during periods of sustained catecholami

146 rms, even upon high-frequency stimulation of chromaffin cells during stress responses.

147 Application of etomidate directly to the chromaffin cells elicited robust catecholamine secretion

148 Evidence suggests that chromaffin cells employ separate mechanisms for evoked e

149 e) Ca2+ and voltage-dependent K+ channels in chromaffin cells exhibit an inactivation that probably a

150 ding potentials to remove inactivation, many chromaffin cells exhibit N-type calcium channel currents

151 Thus chromaffin cells exhibit two kinetically and mechanistic

152 ously reported that N-type current in bovine chromaffin cells exhibits very little voltage-dependent

153 evious studies have shown that naive adrenal chromaffin cells express a nominal Ca(v)3.2-dependent co

154 Recently, we found that chromaffin cells express components of the plasmin(ogen)

155 d secretion from Munc18-1-null mouse adrenal chromaffin cells expressing Munc18-1 mutants designed to

156 residues, single exocytotic events in bovine chromaffin cells expressing R198Q, R198E, K201Q, or K201

157 Single exocytotic events in chromaffin cells expressing this mutant were characteriz

158 arge dense core vesicle (LDCV) exocytosis in chromaffin cells follows a well characterized process co

159 Stimulation of bovine chromaffin cells for 5 min with 6 mum free intracellular

160 at the plasma membrane and in the cytosol in chromaffin cells from adrenal medulla.

161 A30P or wild-type (WT) alpha-syn, as well as chromaffin cells from control and alpha-syn null mice, t

162 We show that adrenal chromaffin cells from CPX II knockout mice exhibit marke

163 Additionally, mRNA analyses of purified chromaffin cells from Gata3 mutants show that levels of

164 e have examined the kinetics of secretion in chromaffin cells from mice lacking phosphatidylinositol

165 ime and characterized in freshly dissociated chromaffin cells from mouse.

166 nctional properties and cell excitability in chromaffin cells from normal and hypophysectomized (pitu

167 SCR-1 calcium-insensitive mutant or by using chromaffin cells from PLSCR-1(-)/(-) mice prevents outwa

168 ar mechanisms by which PGE(2) might modulate chromaffin cell function.

169 grams down-regulate SCP-gene and up-regulate chromaffin cell-gene networks.

170 s highly expressed in bovine adrenomedullary chromaffin cells, human pheochromocytoma tissue, PC12 ph

171 We electrically stimulated chromaffin cells in adrenal tissue slices at the sympath

172 ime-lapse imaging of Lifeact-GFP-transfected chromaffin cells in combination with fluorescent 70 kDa

173 lar sites expressed in intact bovine adrenal chromaffin cells in culture.

174 small and different subpopulations of bovine chromaffin cells in culture.

175 -R(KT) mAb was observed in adrenal medullary chromaffin cells in murine and human tissue.

176 es and other hormones, released from adrenal chromaffin cells in response to Ca(2+) influx through vo

177 to the extent of catecholamine release from chromaffin cells in response to stimulation by carbachol

178 s on T-type Ca(v)3.2 calcium influx in mouse chromaffin cells in situ.

179 Stimulation of chromaffin cells in the presence of a plasma membrane ma

180 catecholamines and a neuropeptide from mouse chromaffin cells in vitro.

181 0 were colocalized to the Golgi apparatus of chromaffin cells in vivo and shared localization with CH

182 We hypothesize that Slo splicing in adrenal chromaffin cells in vivo is differentially regulated by

183 ociated with distinctive membrane changes of chromaffin cells including increased electron density, a

184 evealed decreased LDCV size in noradrenergic chromaffin cells, increased adrenal norepinephrine and e

185 he enhancement of secretion in permeabilized chromaffin cells indicates that N-terminal Rim1 does not

186 ated exocytic function in Mecp2(-/y) adrenal chromaffin cells, indicating that the Mecp2 null mutatio

187 pression of Ca(v)3.2 channels in MPC 9/3L-AH chromaffin cells induced low-threshold secretion that co

188 In chromaffin cells, inhibition of H(+)-ATPase diverted CHG

189 under physiological electrical stimulation, chromaffin cells internalise membrane via two distinct p

190 In chromaffin cells, IRM detects the fusion of individual g

191 ominant calcium signal regulating release in chromaffin cells is generated by the cooperative action

192 Transient stimulation of secretion in calf chromaffin cells is invariably followed by rapid endocyt

193 Exocytosis in adrenal chromaffin cells is strongly influenced by the pattern o

194 heteromeric nAChR expressed by human adrenal chromaffin cells is the alpha3beta4* subtype (asterisk i

195 on of neurotransmitters and neuropeptides in chromaffin cells, is poorly understood.

196 In chromaffin cells isolated from a PICK1 knockout (KO) mou

197 Chromaffin cells isolated from transgenic mice that over

198 analyzed their role in LDCV exocytosis using chromaffin cells lacking individual isoforms.

199 equently, the absence of Snapin in embryonic chromaffin cells leads to a significant reduction of cal

200 These findings suggest one way in which chromaffin cells may regulate cargo release is via diffe

201 Thus, chromaffin cells may regulate release of different trans

202 Mouse chromaffin cells (MCCs) fire spontaneous action potentia

203 e docking, neither synchronized secretion in chromaffin cells nor Ca(2+)-triggered SUV-GUV fusion was

204 exhibiting differential mobility shifting to chromaffin cell nuclear proteins during EMSA, binding of

205 own to accumulate mainly in association with chromaffin cells, occasional nerve endings and macrophag

206 also expressed in neonatal adrenal medullary chromaffin cells of rats and mice whose hypoxia-evoked c

207 To specifically delete GRK2 in the chromaffin cells of the adrenal gland, we crossed PNMTCr

208 Chromaffin cells of the adrenal medulla (AM) represent t

209 Chromaffin cells of the adrenal medulla are a primary ne

210 Chromaffin cells of the adrenal medulla are innervated b

211 c neurons are severely depleted in CIPA, but chromaffin cells of the adrenal medulla are spared.

212 ium channels are expressed in neurosecretory chromaffin cells of the adrenal medulla.

213 opening of a narrow fusion pore, in adrenal chromaffin cells of wild-type and Rab3A(-/-) mice.

214 gs of quantal exocytosis from bovine adrenal chromaffin cells on the device.

215 By culturing chromaffin cells on the VAL-PVC/SiNW-FET, the conductanc

216 ak amplitude of nicotine-induced currents in chromaffin cells or in human embryonic kidney cells ecto

217 cement of exocytosis by PMA in either bovine chromaffin cells or the INS-1 insulin-secreting cell lin

218 ytomas and paragangliomas are rare tumors of chromaffin cell origin.

219 Thus, in chromaffin cells, PKC enhances exocytosis both by increa

220 Internalisation of PrP(d) from the chromaffin cell plasma membrane occurred in association

221 suggest that PROG inhibits CA secretion from chromaffin cells predominantly by rapidly inhibiting nAC

222 The bovine chromaffin cell procedure should yield approximately 10-

223 In cultured chromaffin cells, reducing endogenous CHGA expression by

224 Adrenal chromaffin cells release hormones and neuropeptides that

225 est that a spontaneous syntilla, at least in chromaffin cells, releases Ca2+ into a cytosolic microdo

226 wise, inactivation of the V0 a1-I subunit in chromaffin cells resulted in a decreased frequency and p

227 comparable with those of bPAC1hop in bovine chromaffin cells resulted in acquisition by PC12-G cells

228 hat overexpression of neuronal AP-3 in mouse chromaffin cells results in a striking decrease in the n

229 rometric measurements of exocytosis in mouse chromaffin cells revealed that syb2 TMD mutations altere

230 medullary slices that permit separating the chromaffin cell secretion from sympathetic input.

231 Stimulation of chromaffin cell secretion in vitro triggers not only sec

232 CG10 by synthetic siRNAs virtually abolished chromaffin cell secretion of a transfected CHGA-EAP chim

233 revented the effects of IH on hypoxia-evoked chromaffin cell secretion.

234 extraordinary accumulation of solutes inside chromaffin cell secretory vesicles, although this has ye

235 r with time, that vesicles in bovine adrenal chromaffin cells segregate into distinct populations, ba

236 We provide data to show that chromaffin cells selectively release catecholamine under

237 l firing rates, set by the sympathetic tone, chromaffin cells selectively release catecholamines at a

238 Neuroendocrine chromaffin cells selectively secrete a variety of transm

239 In summary, PAI-1 is expressed in chromaffin cells, sorted into the regulated pathway of s

240 e mice, expressing Cre recombinase under the chromaffin cell-specific phenylethanolamine N-methyltran

241 Chromaffin cells stimulated with high KCl showed both sl

242 ndogenous proteins are expressed in separate chromaffin cell subpopulations.

243 gnals was severalfold faster than in adrenal chromaffin cells, suggesting profound differences in the

244 eterogeneous release of catecholamine at the chromaffin cell surface.

245 ltered transmission at the preganglionic --> chromaffin cell synapse.

246 In bovine chromaffin cells, syntaxin and SNAP-25 colocalize in def

247 Two Syt isoforms are expressed in chromaffin cells: Syt-1 and Syt-7.

248 medulla gland and of cultured human adrenal chromaffin cells that demonstrated prominent expression

249 chains supported secretion in permeabilized chromaffin cells that had been allowed to rundown.

250 hromocytoma is a rare but important tumor of chromaffin cells that is frequently considered in the ev

251 Src family kinases (SFKs) are abundant in chromaffin cells that reside in the adrenal medulla and

252 ase, present in the local environment of the chromaffin cell, that selectively cleaves CgA to generat

253 In cultured chromaffin cells, the total cytosolic catechol concentra

254 irectly activated GABA(A) receptors found in chromaffin cells thereby elevating [Ca(2+)](i).

255 , high-affinity nAChRs expressed in cultured chromaffin cells, they do not appear to be involved in f

256 1 was to greatly increase the sensitivity of chromaffin cells to channel formation by alpha-latrotoxi

257 Stimulation causes chromaffin cells to fire action potentials, leading to t

258 We used bovine chromaffin cells to investigate the effects of PROG on C

259 tentials delivered at 0.5 Hz) causes adrenal chromaffin cells to selectively release catecholamines t

260 hetic tone, basal synaptic excitation drives chromaffin cells to selectively secrete modest levels of

261 CPE and PC activity in extracts of cultured chromaffin cells; total protein levels were unaltered fo

262 In a chromaffin cell-transfected CHGA 3'-UTR/luciferase repor

263 ies have demonstrated that adrenal medullary chromaffin cells transplanted into the spinal subarachno

264 ection of catecholamine release from adrenal chromaffin cells trapped in a microfluidic network.

265 ificity for the diagnosis of adrenomedullary chromaffin cell tumors can be jeopardized by physiologic

266 PC12 cells, like endocrine chromaffin cells, undergo neuronal-like differentiation

267 We studied insertion of granules in bovine chromaffin cells using capacitance as a measure of plasm

268 stics of individual secretory events in calf chromaffin cells using catecholamine amperometry combine

269 ne release in individual quantal events from chromaffin cells using cell-attached patch amperometry.

270 s of exocytosis from populations of mast and chromaffin cells using chemoreceptive neuron MOS (CnuMOS

271 We investigated its role in chromaffin cells using Doc2b knock-out mice and high tem

272 Experiments on diI-stained bovine adrenal chromaffin cells using polarized TIRFM demonstrate rapid

273 strate that CIH increases the RRP in adrenal chromaffin cells via ROS-mediated activation of PKC and

274 Secretion of catestatin intermediates from chromaffin cells was accompanied by the cosecretion of c

275 Endopin 2 in neuroendocrine chromaffin cells was colocalized with the secretory vesi

276 histamine in H(1) receptor/TRPC4-expressing chromaffin cells was comparable with that triggered by a

277 ing of individual exocytotic fusion pores in chromaffin cells was imaged electrochemically with high

278 eover, regulated secretion of endopin 2 from chromaffin cells was induced by nicotine and KCl depolar

279 lamines, measured by amperometry in cultured chromaffin cells, was found to be increased either by pr

280 In Cplx 2-null adrenal chromaffin cells, we also find decreased and desynchroni

281 Here, in adrenal chromaffin cells, we expressed a Munc18 mutant with redu

282 In bovine adrenal chromaffin cells, we found Rac1, but not Cdc42, to be ra

283 ophysiological measurements in mouse adrenal chromaffin cells, we show that PI(4,5)P2 uncaging potent

284 In individual chromaffin cells, we tracked conformational changes in S

285 We show that bovine adrenal chromaffin cells were excited by etomidate at clinically

286 Bovine adrenal chromaffin cells were induced to express Rab3AQ81L and g

287 egulates stimulus-secretion coupling, bovine chromaffin cells were infected with Semliki Forest virus

288 Bovine adrenal chromaffin cells were loaded into the microfluidic chann

289 Bovine adrenal chromaffin cells were superfused with a variety of GABA(

290 Small populations of chromaffin cells were trapped in the microfluidic device

291 vity was also evident in a subset of adrenal chromaffin cells where labeling appeared to be predomina

292 red how alpha-syn overexpression in PC12 and chromaffin cells, which exhibit low endogenous alpha-syn

293 s to hypoxia by the carotid body and adrenal chromaffin cells, which regulate cardio-respiratory func

294 Combined treatment of chromaffin cells with 40 mm KCl, which elevates intracel

295 y monitoring CME of single vesicles in mouse chromaffin cells with cell-attached capacitance measurem

296 Stimulation of chromaffin cells with lysophosphatidic acid, a nonsecret

297 s and whole-cell recordings from rat adrenal chromaffin cells with parallel experiments on inactivati

298 Treatment of cultured bovine adrenal chromaffin cells with the catecholamine transport blocke

299 in each inhibited catecholamine release from chromaffin cells, with superior potency for the shorter

300 foundly impairs priming of granules in mouse chromaffin cells without altering catecholamine release