ライフサイエンスコーパス: secretory vesicle

1 4 receptors and Myo2 motors per transporting secretory vesicle.

2 JA signaling that promotes the formation of secretory vesicles.

3 Ypt32p-GTP to recruit Sec2p to Golgi-derived secretory vesicles.

4 ation that is required for the exocytosis of secretory vesicles.

5 tion for full and partial collapses of large secretory vesicles.

6 rostatic interactions and may associate with secretory vesicles.

7 disorganized trafficking and fusion between secretory vesicles.

8 tilisin-like serine protease SUB1 in exoneme secretory vesicles.

9 5-HT(1B)), was delivered to the dendrites in secretory vesicles.

10 nd is present in purified human neuropeptide secretory vesicles.

11 ess that drives the budding and transport of secretory vesicles.

12 n compromised growth and the accumulation of secretory vesicles.

13 c reticulum (ER) and formation of many large secretory vesicles.

14 (GEF) that activates the Rab GTPase Sec4p on secretory vesicles.

15 ease of small molecules that are packaged in secretory vesicles.

16 (CgB) represent the major proteins of these secretory vesicles.

17 olved proteins only from plasma membranes or secretory vesicles.

18 intermediate forms that are then packed into secretory vesicles.

19 oduction of POMC-derived peptide hormones in secretory vesicles.

20 nsistent with its extralysosomal function in secretory vesicles.

21 , indicating that they function as bona fide secretory vesicles.

22 oviding a mechanism for PTPMEG2 targeting to secretory vesicles.

23 microm) basal cytoplasmic process devoid of secretory vesicles.

24 mogranin A neuropeptides that are present in secretory vesicles.

25 nsporting monoamines from the cytoplasm into secretory vesicles.

26 participates in the docking of a variety of secretory vesicles.

27 e growth and the depolarized accumulation of secretory vesicles.

28 hain, bearing bound IL-4, was mobilized into secretory vesicles.

29 ysaccharide, is trafficked within post-Golgi secretory vesicles.

30 preformed IL-4 from eosinophil granules into secretory vesicles.

31 e to promote Rab1-dependent binding of early secretory vesicles.

32 s6p, which sort selected cargo proteins into secretory vesicles.

33 or CFTR revealed its presence exclusively in secretory vesicles.

34 y1 functions selectively in the transport of secretory vesicles.

35 ology and interconnections of TGN-associated secretory vesicles.

36 nt in the concentration of catecholamines in secretory vesicles.

37 of Myo2 with its receptor, the Rab Sec4, on secretory vesicles.

38 holipid is enriched on the cytosolic face of secretory vesicles.

39 ort proteins at the trans-Golgi network into secretory vesicles.

40 During hyphal, but not yeast growth, secretory vesicles accumulate in an apical body called a

41 defects at a late stage of the pathway, with secretory vesicles accumulating near exocytic sites.

42 d functions to regulate trafficking of early secretory vesicles, activation of T cells, and expressio

43 The regulated secretory vesicle activity, represented by cathepsin B,

44 hizosaccharomyces pombe, Myosin Vs transport secretory vesicles along actin cables, which are dynamic

45 cumulation of solutes inside chromaffin cell secretory vesicles, although this has yet to be demonstr

46 partners that facilitates maturation of the secretory vesicle and helps to promote the directionalit

47 ane proteins and to compare the proteomes of secretory vesicle and plasma membranes.

48 Moreover, F. alocis-induced secretory vesicle and specific granule exocytosis were p

49 in the cytoplasm and also noncanonically in secretory vesicle and tertiary granule compartments.

50 show that myosin-V is activated by binding a secretory vesicle and that myosin-V mutations that compr

51 osine phosphate family located in dense core secretory vesicles and a major autoantigen in type 1 dia

52 run (KR) is an unconventional fusion between secretory vesicles and a target membrane that releases i

53 id formation during packing of peptides into secretory vesicles and amyloid dissociation upon release

54 Cells lacking Boi1/2 accumulate secretory vesicles and are defective in bud growth.

55 -SAAS, which are stored in and released from secretory vesicles and are expressed widely in nervous,

56 Here we track individual secretory vesicles and associated proteins in vivo durin

57 esicle release by promoting coupling between secretory vesicles and calcium channels.

58 rminal signal sequence allowing targeting to secretory vesicles and cytokine secretion, whereas usage

59 ClC-3 to polymorphonuclear leukocytes (PMN) secretory vesicles and demonstrated that it is required

60 shworks, and both caused homotypic fusion of secretory vesicles and formation of aqueous vacuoles in

61 his agent inhibited stimulated exocytosis of secretory vesicles and gelatinase and specific granules

62 ves a dual function, to both recruit Sro7 to secretory vesicles and inhibit its Rab-dependent tetheri

63 primary CPECs, including self-assembly into secretory vesicles and integration into endogenous choro

64 Recent evidence indicates that secretory vesicles and machinery are essential component

65 Ypt11, receptors for essential transport of secretory vesicles and mitochondria, respectively, bind

66 of IA-2 and IA-2beta, structural proteins of secretory vesicles and modulators of neuroendocrine secr

67 ons correspond to a paucity of foveolar cell secretory vesicles and notable loss of stomach but not i

68 cellular material into the bud: Myo2p moves secretory vesicles and organelles, whereas Myo4p transpo

69 Myo2p moves cargo including secretory vesicles and other organelles for several micr

70 e of phosphatidylserine in lipid bilayers of secretory vesicles and plasma membranes couples the doma

71 The zinc transporter ZnT2 imports zinc into secretory vesicles and regulates zinc export from the ma

72 ssibly modified in the acidic compartment of secretory vesicles and requiring a release mechanism tha

73 roups redundantly mobilize G2A latent within secretory vesicles and result in G2A receptor/Galphai/ph

74 ClC-3 protein was detected in the secretory vesicles and secondary granules of resting PMN

75 This interaction normally occurs on secretory vesicles and serves to couple nucleotide excha

76 proximately 3-fold increase in the number of secretory vesicles and the insulin content of cells.

77 hosphorylated after it has been recruited to secretory vesicles and the level of PI(4)P has been redu

78 ing pathway, increasing zinc accumulation in secretory vesicles and zinc secretion.

79 transmitters bind to a charged matrix within secretory vesicles, and release requires entry of counte

80 d CSLF6 to the endoplasmic reticulum, Golgi, secretory vesicles, and the PM and CSLH1 to the same loc

81 Both types of secretory vesicles appear to fuse into a type of prevacu

82 embrane system and packaged in Golgi-derived secretory vesicles, Arabidopsis (Arabidopsis thaliana) s

83 dhesive ligands mobilized from intracellular secretory vesicles are capped to the posterior end of th

84 Here we found that most secretory vesicles are delivered by myosin-V on linear a

85 n proteins suggests that the hypothesis that secretory vesicles are formed from plasma membranes by e

86 Secretory vesicles are neutrophil intracellular storage

87 Proteases within secretory vesicles are required for conversion of neurop

88 Secretory vesicles are required for release of chemical

89 ds perceive the haptoelectrical stimulation, secretory vesicles are tailored to be released in a sequ

90 In budding yeast, secretory vesicles are transported by the myosin-V Myo2p

91 In higher eukaryotes, secretory vesicles are transported to the plasma membran

92 Secretory vesicles are used during spermatogenesis to de

93 to synaptic vesicles and to large dense-core secretory vesicles as reported previously, whereas synap

94 vesicles recruited during phagocytosis were secretory vesicles as their recruitment was sensitive to

95 ents are brought to these sites by riding on secretory vesicles as they are actively transported alon

96 log, proprotein convertase 1/3, activates in secretory vesicles at a pH of 5.5.

97 Osh4p associates with secretory vesicles at least in part through its interact

98 exocytic machinery responsible for fusion of secretory vesicles at specific sites on the plasma membr

99 oproteins residing at the egg surface and in secretory vesicles at the egg cortex.

100 exocyst mediates the tethering of post-Golgi secretory vesicles at the plasma membrane for exocytosis

101 eric protein complex that tethers post-Golgi secretory vesicles at the plasma membrane for exocytosis

102 n complex implicated in tethering post-Golgi secretory vesicles at the plasma membrane in preparation

103 t, a conserved multiprotein complex, tethers secretory vesicles before fusion with the plasma membran

104 The tethering of the secretory vesicles before membrane fusion is mediated by

105 ynthase Mcs1 moves to the plasma membrane in secretory vesicles, being delivered by kinesin-1 and myo

106 secreted with catecholamines and crucial for secretory vesicle biogenesis in neuronal/neuroendocrine

107 Secretory vesicle budding (COPII) detected by the packag

108 asplakinolide rapidly disrupted transport of secretory vesicles, but each drug caused distinct respon

109 cal for the docking and fusion of post-Golgi secretory vesicles, but not for their transport to the P

110 d on the Golgi is normally incorporated into secretory vesicles, but the fate of that pool has been u

111 We propose that the exocyst is recruited to secretory vesicles by the combinatorial signals of Sec4-

112 Sec2p is recruited to secretory vesicles by the upstream Rab Ypt32p acting in

113 that increased sequestration of dopamine in secretory vesicles by VMAT2 is protective for PD.

114 at when Uso1 is inappropriately recruited to secretory vesicles by Ypt1-SW1(Sec4), the extended coile

115 its host cell requires protein release from secretory vesicles, called dense granules, to maintain t

116 These include peroxisomes, secretory vesicles, cargoes of Myo2p, and ASH1 mRNA, a c

117 In budding yeast, two classes of post-Golgi secretory vesicles carrying different sets of cargoes ty

118 was mainly due to elevated concentration of secretory vesicles close to the cell membrane.

119 ia a fusion pore that then dilates until the secretory vesicle collapses into the PM; or by "kiss-and

120 Non-classical secretory vesicles, collectively referred to as extracel

121 for the targeting of this phosphatase to the secretory vesicle compartment by association with other

122 ibuted throughout the cytoplasm and numerous secretory vesicles concentrated near the locular side.

123 localizes to a distinct class of peptidergic secretory vesicles containing IGF-1.

124 ertebrate MICAL-1 regulates the targeting of secretory vesicles containing immunoglobulin superfamily

125 toward the cell membrane and filopodia, and secretory vesicles containing the HSP90alpha-AHA1-surviv

126 membrane, the endoplasmic reticulum and the secretory vesicles contribute to the milk fat globule me

127 otein architecture of the 'human' dense core secretory vesicles (DCSV) to understand mechanisms for s

128 ng the bud-mother axis, providing tracks for secretory vesicle delivery.

129 ntly, cathespin L expression was directed to secretory vesicles, demonstrated by colocalization of ca

130 nt cell type is unique in containing a giant secretory vesicle derived from the Golgi apparatus.

131 cate that XGA is secreted by a novel type of secretory vesicles derived from trans-Golgi cisternae.

132 Because acidification of catecholamine secretory vesicles determines CHGA trafficking and proce

133 with redistribution of CypB(W128A)-GFP into secretory vesicles disconnected from the ER/Golgi networ

134 e cell plasma membrane, where membrane-bound secretory vesicles dock and fuse to release intravesicul

135 Secretory vesicles dock by multiple, PI(4,5)P2-dependent

136 The acidity of mammalian secretory vesicles drives concentration and processing o

137 iate the recruitment of exocyst subunits and secretory vesicles during exocytosis.

138 d mechanism for recruitment of Golgi-derived secretory vesicles during phagosome biogenesis, which wa

139 d that PI(4)P is required for late Golgi and secretory vesicle dynamics and targeting and, as a resul

140 itro and induced redistribution of CTSB to a secretory vesicle-enriched fraction.

141 teins from both plasma membrane-enriched and secretory vesicle-enriched fractions.

142 mbrane-enriched fractions, 418 (37%) only in secretory vesicle-enriched membrane fractions, and 127 (

143 olved in the calcium-dependent regulation of secretory vesicle exocytosis in neurons and neuroendocri

144 Understanding the functional consequences of secretory vesicle exocytosis requires knowledge of their

145 phatase (V-ATPase) is directly implicated in secretory vesicle exocytosis through a role in membrane

146 sma membrane where it functions in regulated secretory vesicle exocytosis, but it is also found on in

147 te mechanisms and functional consequences of secretory vesicle exocytosis.

148 ament (F-actin) coats around the exocytosing secretory vesicles followed by direct retrieval of some

149 g a positive-feedback loop that prepares the secretory vesicle for fusion with the plasma membrane.

150 About ten motors associate with each secretory vesicle for rapid transport to sites of cell g

151 crucial step in the tethering of post-Golgi secretory vesicles for exocytosis.

152 nt, budding yeast grows rapidly transporting secretory vesicles for localized growth and actively seg

153 transporter 3 (VGLUT3) loads glutamate into secretory vesicles for neurotransmission and is expresse

154 to provide an essential role in delivery of secretory vesicles for polarized growth and in the trans

155 olytic fragments that function in chromaffin secretory vesicles for release of bioactive molecules fo

156 that CHV1 utilizes trans-Golgi network (TGN) secretory vesicles for replication.

157 promoting recruitment of Sec2p by Ypt32p as secretory vesicles form.

158 Granins regulate secretory vesicle formation in neuroendocrine cells and

159 In its absence, secretory vesicle formation is impaired, leading to accu

160 ction of microvilli, and marked increases in secretory vesicle formation.

161 owed that G2A resides in the plasma membrane/secretory vesicle fraction and not in neutrophil primary

162 lysis, MRP-14 was present in plasma membrane/secretory vesicle fractions and gelatinase and specific

163 P bound Sec4p is required for the transit of secretory vesicles from the trans-Golgi to sites of pola

164 The newly defined secretory vesicle function of cathepsin L for biosynthes

165 (syt), a transmembrane protein localized to secretory vesicles, functions as a Ca2+ sensor that faci

166 a ubiquitous process in eukaryotes, whereby secretory vesicles fuse with the plasma membrane and rel

167 to occur either by "full fusion," where the secretory vesicle fuses with the plasma membrane (PM) vi

168 ng the apical plasma membrane at the site of secretory vesicle fusion and re-assembled directionally

169 C2B domain of Synaptotagmin-1 participate in secretory vesicle fusion, and in more upstream steps, es

170 tant are associated with the perturbation of secretory vesicle genesis from the TGN.

171 CAV1 is localized in the plasmalemma, secretory vesicles, Golgi, mitochondria, and endoplasmic

172 h HCN channels, which are located on or near secretory vesicles, have an important role in modulating

173 cellular structures that are consistent with secretory vesicles, however, in most cell types studied,

174 pool or by Ca(2+)-dependent exocytosis from secretory vesicles, i.e., by a mechanism similar to the

175 hat affect the recruitment of the exocyst to secretory vesicles identified genes encoding clathrin an

176 ules correlated with the positions of single secretory vesicles in a functionally rescued Munc18-1-nu

177 ere we show that vti1a is absent from mature secretory vesicles in adrenal chromaffin cells, but loca

178 CHGA) is coreleased with catecholamines from secretory vesicles in adrenal medulla and sympathetic ax

179 ired for the formation of large, specialized secretory vesicles in gastric zymogenic (chief) cells (Z

180 nsporter properly localized to intracellular secretory vesicles in HC11 and MCF-7 cells.

181 ored in, and secreted from, large dense-core secretory vesicles in nerve terminals in the median emin

182 c vesicle glycoprotein 2A (SV2A) is found in secretory vesicles in neurons and endocrine cells.

183 Mini202, we measured the pH of catecholamine secretory vesicles in PC-12 cells (pH approximately 5.9)

184 eviously unprecedented role of Golgi-derived secretory vesicles in phagocytic uptake, the key innate

185 ells, as well as accumulation of unpolarized secretory vesicles in the latter mutant cells.

186 th the tether and the motor reside on moving secretory vesicles in yeast cells, a necessary feature f

187 that Rab26 selectively directs synaptic and secretory vesicles into preautophagosomal structures, su

188 te and instead rapidly reseals such that the secretory vesicle is retrieved almost fully intact.

189 ne (PS) in the mammalian plasma membrane and secretory vesicles is maintained, in part, by an ATP-dep

190 Post-Golgi transport of secretory vesicles is mediated by the Rab GTPase Sec4, a

191 Thus, the marked acidity of mammalian secretory vesicles is not conserved in evolution, and a

192 organized, analysis of directed transport of secretory vesicles is still biased toward the bud, refle

193 (ATPase II), originally isolated from bovine secretory vesicles, is a member of this subfamily based

194 In mammalian cells, cargo-laden secretory vesicles leave the endoplasmic reticulum (ER)

195 nofluorescence was detected in lysosomes and secretory vesicle-like organelles in LG acinar cells and

196 ulation through a role in modulating insulin secretory vesicle localization and/or fusion via actin r

197 acts in retrograde trafficking by returning secretory vesicle material to the trans-Golgi network.

198 he actin coats results from the union of the secretory vesicle membrane and PM and that this compartm

199 ged regions in SNARE proteins in synaptic or secretory vesicle membrane lipid bilayers with positivel

200 logies to develop a more complete catalog of secretory vesicle membrane proteins and to compare the p

201 VGF cofractionated with secretory vesicle membranes but was not detected in dete

202 ion precedes actin and myosin recruitment to secretory vesicle membranes.

203 a fusion pore opens between the plasma and a secretory vesicle membranes; typically, when the pore di

204 Previous in vitro studies have found that secretory vesicle motion at many sites of release is con

205 photobleaching analysis, we first show that secretory vesicles move toward and accumulate at the tip

206 erved surface residues that are required for secretory vesicle movement, but not vacuole movement.

207 atrunculinA resistant, leading to defects in secretory vesicle movement.

208 on of cathepsin V with enkephalin and NPY in secretory vesicles of human neuroblastoma cells was illu

209 the gelatinase and specific granules and the secretory vesicles of human PMNs.

210 n the plasma membrane and in the membrane of secretory vesicles of isolated rat lactotrophs.

211 the cytoplasm, RIG-I and MDA-5 are stored in secretory vesicles of neutrophils and showed that RIG-I

212 TgCPC1 and TgCPC2 localize to constitutive secretory vesicles of tachyzoites, the dense granules.

213 We show that actin-coated secretory vesicles of the exocrine pancreas travel this

214 e increased levels of (Met)enkephalin within secretory vesicles of the regulated secretory pathway.

215 t in a massive accumulation of intracellular secretory vesicles or their cargoes.

216 complex and Rab11 GTPase Ypt3 help to tether secretory vesicles or tubulovesicular structures along t

217 nalysis of membrane-bound containers such as secretory vesicles, organelles, and exosomes can provide

218 at the > or =30-fold (H+) difference between secretory vesicles (pH < or = 5.7) and the cytoplasm (pH

219 lutamate)-SNARE essential for Ca2+-dependent secretory vesicle-plasma membrane fusion in neuroendocri

220 CD45, confirming mobilization of the labile secretory vesicle pool.

221 s up cytosolic monoamines into intracellular secretory vesicles, preventing their neurotoxicity in th

222 two-hybrid screening identified a number of secretory vesicle proteins that interacted directly with

223 ntigens in type 1 diabetes and transmembrane secretory vesicle proteins, results in impaired secretio

224 les released during the fusion of individual secretory vesicles provides information about molecular

225 r, the trans-Golgi network Rab Ypt31/32p and secretory vesicle Rab Sec4p each bind directly, but dist

226 n in the biogenesis or maintenance of mature secretory vesicles, raising the possibility of a complet

227 the plasma membrane, tethering and fusion of secretory vesicles require the exocyst complex.

228 dependent of the endoplasmic reticulum/Golgi secretory vesicle route.

229 Here we show that on secretory vesicles SEC2 mRNA is physically associated wi

230 domains of positively charged amino acids of secretory vesicle SNARE proteins with similar domains of

231 of at least 24 carbon atoms are enriched in secretory vesicle subdomains of the TGN and are critical

232 his loop results in a modest accumulation of secretory vesicles, suggesting impaired exocyst function

233 Post-Golgi secretory vesicles (SVs) containing the RAB11 orthologue

234 intermolecular steps via which they prepare secretory vesicles (SVs) for fusion is key to understand

235 Secretory vesicle targeting and fusion require a conserv

236 residues 1-261, as the region containing the secretory vesicle targeting signal.

237 The temporary adhesive secretory vesicles (TASV) are released from the gland ce

238 Secretory vesicles tether to the plasma membrane very re

239 determining the sites at the membrane where secretory vesicles tether.

240 qt-SM is enriched in a subset of TGN-derived secretory vesicles that are also enriched in a glycophos

241 n in the swarming colony, ideally suited for secretory vesicles that diffuse poorly.

242 that control biogenesis and fusion of early secretory vesicles that exit the ER and host proteins th

243 VMAT2 thus defines a population of secretory vesicles that mediate the activity-dependent s

244 tion of beta-secretase activity in regulated secretory vesicles that produce beta-amyloid (Abeta).

245 dentification of the major proteins in these secretory vesicles that provide dynamic storage and secr

246 nules of adrenal medulla represent regulated secretory vesicles that secrete neuropeptides and catech

247 The exocyst serves to tether secretory vesicles to cortical sites specified by polari

248 Sec2p, is needed for polarized transport of secretory vesicles to exocytic sites and for exocytosis.

249 cated Sec3p subunit is capable of recruiting secretory vesicles to mitochondria.

250 Beta cells from nondiabetic mice transfer secretory vesicles to phagocytic cells.

251 g by E-Syt1 (ER to PM) and by synaptotagmin (secretory vesicles to PM) undergo a similar regulation b

252 pathway, from the endoplasmic reticulum via secretory vesicles to release into the interstitial spac

253 complex required for targeting and fusion of secretory vesicles to sites of exocytosis at the plasma

254 exocyst subunits, which function in docking secretory vesicles to sites of polarized secretion, in t

255 multiprotein complex essential for tethering secretory vesicles to specific domains of the plasma mem

256 complex plays an essential role in tethering secretory vesicles to specific domains of the plasma mem

257 lex that has been implicated in tethering of secretory vesicles to specific regions on the plasma mem

258 MyoVc has been implicated in transporting secretory vesicles to the apical membrane [5].

259 exocyst complex is required for tethering of secretory vesicles to the apical plasma membrane.

260 he activity of molecular motors that deliver secretory vesicles to the growth region or which mediate

261 ex implicated in the tethering of post-Golgi secretory vesicles to the plasma membrane before fusion.

262 was believed to target and tether post-Golgi secretory vesicles to the plasma membrane during exocyto

263 hat align in a side-by-side manner to tether secretory vesicles to the plasma membrane in preparation

264 rmissive conditions, although trafficking of secretory vesicles to the plasma membrane is unimpaired,

265 complex mediates the tethering of post-Golgi secretory vesicles to the plasma membrane prior to fusio

266 eric effector of Sec4p involved in tethering secretory vesicles to the plasma membrane.

267 It requires the delivery of post-Golgi secretory vesicles to the site of polarized growth.

268 is process involves the polarized traffic of secretory vesicles to the Spitzenkorper (SPK) and their

269 sicaceae dry stigma to deliver cargo-bearing secretory vesicles to the stigmatic papillar plasma memb

270 Transport of SEC2 mRNA on secretory vesicles to the tip localizes SEC2 translation

271 d growth requires the continuous delivery of secretory vesicles to the tip region.

272 able actin cables, accompanied by defects in secretory vesicle traffic during polarized growth and se

273 cturally altered cables, along with impaired secretory vesicle traffic.

274 ents though it is believed to participate in secretory vesicle trafficking in vertebrate cells.

275 Post-Golgi secretory vesicle trafficking is a coordinated process,

276 ion inhibits a vesicle "priming" step, after secretory vesicle trafficking to "docking" sites but bef

277 cle of myosin-V in its essential function of secretory vesicle transport along actin cables in yeast.

278 Myo2-mediated transport processes, including secretory vesicle transport, mitochondrial inheritance,

279 shape, and velocity and, in turn, efficient secretory vesicle transport.

280 that intracellular cytokine receptors within secretory vesicles transport their cognate cytokines req

281 Before secretory vesicles undergo exocytosis, they must recruit

282 orted, the motors remain associated with the secretory vesicles until they undergo exocytosis.

283 pon the corelease of glutamate and zinc from secretory vesicles via exocytosis.

284 (diameter approximately 200 nm), a model for secretory vesicles, were prepared by extrusion and loade

285 and Snc2p from the plasma membrane into new secretory vesicles where they act to recruit the exocyst

286 he trans-Golgi network and possibly immature secretory vesicles, where it may be involved in the form

287 ytoplasmic face of the enclosing membrane of secretory vesicles, where it regulates vesicle size by p

288 th is supported by tip-directed transport of secretory vesicles, which accumulate temporarily in a st

289 hese cells have an abundance of large apical secretory vesicles, which contain highly glycosylated ma

290 meric protein complex required for tethering secretory vesicles, which is a prerequisite for membrane

291 ve peptides are packaged in large dense-core secretory vesicles, which mediate regulated secretion by

292 e hypothesis is that diffusion can transport secretory vesicles, while actin plays a regulatory role

293 In many animals, the acrosome is a secretory vesicle with exocytosis essential for sperm pe

294 dundantly with Boi1 to promote the fusion of secretory vesicles with the plasma membrane at sites of

295 re required for a late step in the fusion of secretory vesicles with the plasma membrane of the growi

296 Exocytosis involves fusion of secretory vesicles with the plasma membrane, thereby del

297 te for cytoskeletal remodeling and fusion of secretory vesicles with the plasma membrane.

298 ause of an intrinsic defect in the fusion of secretory vesicles with the plasma membrane.

299 lminating in the calcium-dependent fusion of secretory vesicles with the plasma membrane.

300 vesicle trafficking and ultimately fusion of secretory vesicles with the plasma membrane.