ライフサイエンスコーパス: epithelial cell

1 cells as well as monocytes, macrophages, and epithelial cells).

2 maze-like patterns on the surface of mucosal epithelial cells.

3 ) and 'non-professional' phagocytes, such as epithelial cells.

4 facilitated by the synthetic TAR RNA in oral epithelial cells.

5 fibroblasts moved at an increased speed over epithelial cells.

6 y and invasiveness of TNBC and benign breast epithelial cells.

7 olarization and zonula adherens formation in epithelial cells.

8 h cells within glomeruli and collecting duct epithelial cells.

9 signals of the 2 miR expression in alveolar epithelial cells.

10 internalization and endosomal trafficking in epithelial cells.

11 d live influenza A virus (IAV) in human lung epithelial cells.

12 that are highly expressed in vertebrate lens epithelial cells.

13 nprotein bacterial constituents into gastric epithelial cells.

14 helial cells and insulin-sensitive bronchial epithelial cells.

15 ies of cGAS, STING, and PYHINs in human lung epithelial cells.

16 F-beta-mediated permeability across alveolar epithelial cells.

17 crisis with oncogenic potential in prostate epithelial cells.

18 ion and promotes cell cycle entry of tubular epithelial cells.

19 restricted self-antigens in medullary thymic epithelial cells.

20 nto autophagosomes for degradation in airway epithelial cells.

21 production and cellular adaptation in kidney epithelial cells.

22 itself and ST2 protein expression in airway epithelial cells.

23 moides bakeri that get into mouse intestinal epithelial cells.

24 to form biofilm and had reduced survival in epithelial cells.

25 e translocation efficiency across intestinal epithelial cells.

26 rom the basolateral to the apical surface of epithelial cells.

27 itro, with minimal effect on normal prostate epithelial cells.

28 genic KRAS on the cell surface of intestinal epithelial cells.

29 ly to make their initial host encounter with epithelial cells.

30 are conditionally co-expressed in prostatic epithelial cells.

31 a notable phenotype in nontransformed breast epithelial cells.

32 in FPR1-mediated wound healing in intestinal epithelial cells.

33 idative DNA damage) in podocytes and tubular epithelial cells.

34 antly increased in number surrounding breast epithelial cells.

35 ressing dendritic cells, B cells, and thymic epithelial cells.

36 transition leading to increased migration of epithelial cells.

37 rectal cancer cells, but not to normal colon epithelial cells.

38 ARID1A(WT) and ARID1A(KO) human endometrial epithelial cells.

39 tional actin cortex in intestinal and kidney epithelial cells.

40 in both HeLa and polarized Caco2 intestinal epithelial cells.

41 JT in differentiated primary human bronchial epithelial cells.

42 intracellular bacterial pathogens of mucosal epithelial cells.

43 he presentation of HLA-B, -C, and -E on lung epithelial cells.

44 eterogeneous by clustering analysis than the epithelial cells.

45 he population level in human retinal pigment epithelial cells.

46 ncogene activation on this process in normal epithelial cells.

47 nd muc5ac mRNA expression in cultured airway epithelial cells.

48 that block EBV and KSHV infection of target epithelial cells.

49 ALOX15 was predominantly expressed by epithelial cells.

50 the cortical cytoskeleton in normal mammary epithelial cells.

51 primary ADPKD and normal human kidney (NHK) epithelial cells.

52 o the binding to integrins on the surface of epithelial cells.

53 , IL-1beta and Cxcl-1) and also apoptosis of epithelial cells.

54 to productive replication in inducible SLK (epithelial) cells, absence of detectable involvement of

55 hiolar hyperplasia, proliferations of type 2 epithelial cells, accumulations of macrophages, edema an

56 f 632 colonies derived from single bronchial epithelial cells across 16 subjects.

57 t from reproducible availability of alveolar epithelial cells (AEC).

58 wer airway tissues, primary type II alveolar epithelial cells (AECIIs), and the mouse lung cell line

59 treated HO-exposed mice and primary alveolar epithelial cells (AECs) with the novel TREK-1 activators

60 17 and miR-548b were upregulated in alveolar epithelial cells after CI/EVR, which merit further explo

61 CE2 suggests tongue keratinocytes, olfactory epithelial cells, airway club cells and respiratory cili

62 d a gene and protein signature similar to an epithelial cell and gained chromatin accessibility sites

63 eased the proliferation of human colon tumor epithelial cells and blunted H(2)O(2)-induced STAT3 phos

64 immortalised bovine alveolar type II (BATII) epithelial cells and bovine pulmonary arterial endotheli

65 is present in nasal, tracheal, and bronchial epithelial cells and constitutes a central element of th

66 -stimulated gene (ISG) in vitro using airway epithelial cells and extend our findings to in vivo vira

67 (TRPV3) agonists can affect human bronchial epithelial cells and highlight novel physiological and p

68 to characterize the transcriptome of midgut epithelial cells and identified 22 distinct clusters rep

69 in 4 (OLFM4) is expressed in normal prostate epithelial cells and immortalized normal human prostate

70 primary swine nasal and tracheal respiratory epithelial cells and immortalized swine nasal epithelial

71 lial cell types: insulin-insensitive corneal epithelial cells and insulin-sensitive bronchial epithel

72 of fungal metabolites, which can be toxic to epithelial cells and lead to barrier dysfunction.

73 it alters nutrient metabolism in intestinal epithelial cells and microbiome, leading to increased la

74 larity (PCP) pathway is required in alveolar epithelial cells and myofibroblasts for alveologenesis i

75 led specialized synaptic connections between epithelial cells and nerve fibers and studies using opto

76 it enhances viral replication in human lung epithelial cells and primary human airway tissues by inc

77 pathway analysis were performed in bronchial epithelial cells and replicated.

78 AC8 was primarily expressed in renal tubular epithelial cells and time-dependently upregulated.

79 teract with host mucins lining the glandular epithelial cells and trigger inflammation.

80 share the ability to attach and invade oral epithelial cells, and from there each undergoes its own

81 the most upregulated pathway in sEV-treated epithelial cells, and genetic or pharmacologic targeting

82 Innate immune cells, epithelial cells, and many other cell types are capable

83 ormal human primary or immortalized prostate epithelial cells, and their differentiation capability w

84 These are gut sensory epithelial cells, and those that form synapses are refer

85 ST6Gal-I expression in blocking homeostatic epithelial cell apoptosis in gastric cancer pathogenesis

86 Although epithelial cells are among the first to encounter pneumo

87 levels of antimicrobial peptide derived from epithelial cells are reduced but the expression of lipid

88 Although immune and epithelial cells are thought to be the canonical orchest

89 c Pg-strains to invade human-retinal pigment epithelial cells(ARPE-19), their survival, intracellular

90 are complex tissues composed of transformed epithelial cells as well as cancer-activated fibroblasts

91 Moreover, we reveal a lung cancer epithelial cell-autonomous function for p38alpha promoti

92 , we provide evidence that a thermogenic fat-epithelial cell axis regulates intestinal disease tolera

93 ction, we studied an ex vivo human bronchial epithelial cell (BEC)/human lung fibroblast (HLF) cocult

94 g mesenchymal neighbors, while its overlying epithelial cells become WNT-restricted.

95 tic and epigenetic alterations in colorectal epithelial cells but also affect the gut microbiota and

96 demonstrate viral tropism for choroid plexus epithelial cells but little to no infection of neurons o

97 (AKI) with adaptive proliferation of tubular epithelial cells, but repair can also lead to fibrosis a

98 lori's ability to delay apoptosis in gastric epithelial cells by actively driving the degradation of

99 R2) is strongly upregulated on renal tubular epithelial cells by acute cell-mediated rejection (ACR.

100 SCCs were distinguished from the surrounding epithelial cells by calretinin and phospholipase C140 im

101 vival factor for functionally differentiated epithelial cells by expressing a hyperactive STAT5 mutan

102 Primary alveolar epithelial cells can be derived from human lung tissue b

103 ll of origin and the cancer subtype, as most epithelial cells can be reprogrammed toward diverse lung

104 innate immune signaling, in HT-29 intestinal epithelial cells challenged with TNF-alpha or STS.

105 application initiates changes in intestinal epithelial cell characteristics relative to those of sta

106 Here we review recent studies on how colon epithelial cells communicate directly with colon afferen

107 n of MNV receptor (CD300lf) in human HEK293T epithelial cells conferred susceptibility to MNV infecti

108 Insect epithelial cells contain cellular extensions such as bri

109 quisition of mesenchymal phenotypes by tumor epithelial cells contribute to metastasis?

110 levels of ST6GAL-I and SOX9 in human gastric epithelial cells correlated positively with one another

111 -infected canine and feline lungs and airway epithelial cells could serve as higher animal models to

112 ary ACE2 expression in vitro in human airway epithelial cell cultures and in vivo in mouse models of

113 uman intestinal enteroids (HIEs) are primary epithelial cell cultures that can provide insights into

114 lergens was evaluated on primary human nasal epithelial cell cultures.

115 RSV-induced epithelial cell death was associated with increased phos

116 l5, identify a pathogenic Cdkl5-Sox9 axis in epithelial cell-death, and support CDKL5 antagonism as a

117 d the infection of HEK293 and HEK293 T human epithelial cells, deficient in cGAS and in cGAS and STIN

118 al thickness (34%; P < 0.001), and increased epithelial cell density (13%; P < 0.001).

119 We evidence changes in epithelial cell density and distribution in C57/BL6J mic

120 pendent H33258 uptake was rarely observed in epithelial cells derived from the ectocervix and transfo

121 The epithelial cell-derived danger signal mediators thymic s

122 mpare the role of myeloid- versus intestinal epithelial cell-derived IL-33 during dextran sodium sulf

123 estrains colitic disease, whereas intestinal epithelial cell-derived IL-33 is dispensable.

124 oproliferative diseases/lymphomas as well as epithelial cell-derived nasopharyngeal cell carcinoma.

125 Pax2 expression ends once the epithelial cells differentiate into mature proximal and

126 actors and plays an important role in thymic epithelial cell differentiation and development.

127 of selected Par proteins in blastomeres and epithelial cells during the embryogenesis of the ctenoph

128 s demonstrated that LAMP3 expression induces epithelial cell dysfunction leading to apoptosis.

129 can blunt inflammatory signaling in alveolar epithelial cells (ECs) by transcellular delivery of supp

130 silico and in vitro using human endometrial epithelial cells (EEC) grown as monolayers or a 3-dimens

131 herapeutically relevant cell types including epithelial cells, endothelial cells, B cells, T cells an

132 sulted in increased Myc abundance in tubular epithelial cells, enhanced glycolysis, and suppression o

133 ice deficient in Chd4 specifically in thymic epithelial cells exhibited autoimmune phenotypes, includ

134 Here, we describe how regenerating biliary epithelial cells express Wnt-Planar Cell Polarity signal

135 Here, we show that intestinal epithelial cells expressing IRE1beta have an attenuated

136 Strikingly, medullary thymic epithelial cells expressing the autoimmune regulator wer

137 in IL-13 biology to determine whether airway epithelial cell expression of 2 key mediators critical f

138 alignancy cascade, indicating that increased epithelial cell expression of ST6Gal-I is associated wit

139 lucidate a mechanism of action on intestinal epithelial cells for extracellular CDNs.

140 Gingival epithelial cells form an anatomic architecture that conf

141 In human bronchial epithelial cells, formoterol, a long-acting beta (2)-adr

142 g gene expression data from nasal and airway epithelial cells from children and adults with asthma an

143 elium to define transcriptomes of individual epithelial cells from healthy BALB/c mice (controls) and

144 -ATPase mRNA were determined in the cultured epithelial cells from lenses of the two types of mice.

145 cipher the transcriptome of freshly isolated epithelial cells from normal and IPF lungs to discern di

146 TMPRSS2 expression ex vivo in primary airway epithelial cells from participants with and without type

147 anisms include podocyte (visceral glomerular epithelial cell/GEC) injury.

148 In A549 and BEAS-2B pulmonary epithelial cells, glucocorticoids induce KLF9 expression

149 axis essential for stromal cells to modulate epithelial cell growth during intestinal regeneration an

150 table for the study of any kind of monolayer epithelial cells growth.

151 In human lung epithelial cells, GSK3008348 induces rapid internalizati

152 Type 2 inflammatory conditions, human airway epithelial cells (HAECs) generate proferroptotic hydrope

153 ggest that promoting the survival of gastric epithelial cells has implications not only for H. pylori

154 l types, the cytoplasmic function of YAP1 in epithelial cells has not been well studied.

155 C6, we demonstrated that AC6 knockout airway epithelial cells have longer cilia compared with the WT

156 outgrowth forms through extreme increases in epithelial cell height.

157 -culture on patient-derived human intestinal epithelial cells (HIECs), and incorporate perfused vascu

158 have elevated expression of HLA-DR in tumor epithelial cells; HLA-DR expression was also significant

159 orphic Rag mutations while preserving thymic epithelial cell homeostasis.

160 r macrophages and primary human small airway epithelial cells (HSAEpCs) from patients with COPD.

161 Using mice with inducible intestinal epithelial cell (IEC)-specific deletion of Phb1 (Phb1(iD

162 Here, we integrated intestinal epithelial cells (IEC) derived from human intestinal org

163 Intestinal epithelial cells (IEC) exclusively express the desmosoma

164 Among barrier cells, intestinal epithelial cells (IECs) are particularly dependent on ty

165 Myeloid cells interact with intestinal epithelial cells (IECs) by producing various mediators;

166 ells as a model, we observed that intestinal epithelial cells (IECs) were permissive to EV-A71 infect

167 hematopoietic and mesenchymal cells, but not epithelial cells (IECs), in the intestine.

168 In human epithelial cells, IFN-lambda1 production was also induce

169 tein of the LINC complex of fibroblastic and epithelial cells in culture.

170 By imaging epithelial cells in intact ChP explants, we observed cal

171 l cells, with reduced expression in alveolar epithelial cells in IPF lungs.

172 that TGFbeta1 activity is reduced in breast epithelial cells in obesity.

173 Cytokine production by vaginal epithelial cells in response to lactobacilli in the pres

174 y expressed in neutrophils, macrophages, and epithelial cells in response to wounding.

175 chromatin remodeling machinery in intestinal epithelial cells in the colitis response and shows how a

176 ow two extragenic CREs that are prominent in epithelial cells in the lung, regulate expression of the

177 RS-CoV-2 replication in primary human airway epithelial cells in vitro-both prophylactic and therapeu

178 membrane herniations in the apical domain of epithelial cells, indicative of cortex abnormalities.

179 ifferentiation of the human prostate luminal epithelial cells induced by caAKT1 and c-Myc and reveals

180 The tropism of EBV for B cells and epithelial cell infection has been well characterized, b

181 How intestinal epithelial cells interact with the microbiota and how th

182 splaying characteristic conversion of planar epithelial cells into multipolar and invasive mesenchyma

183 eas the function of individual mature thymic epithelial cells is compromised only modestly.

184 However, when proliferation of resident epithelial cells is impaired, alternative regeneration m

185 to maintain adhesion in confluent sheets of epithelial cells is not known.

186 behavior, but how this signal is received by epithelial cells is unknown.

187 chnique to measure the tension in individual epithelial cell junctions of cells in various locations

188 Epithelial cells kept their original levels of prolifera

189 s a premalignant phenotype of normal mammary epithelial cells lacking PTEN.

190 sion of miR-183 cluster in the human retinal epithelial cells leads to the reprogramming and transfor

191 we differentiated the nontumorigenic breast epithelial cell line (MCF10A) from its cancerous PTEN mu

192 transiently disrupted TJs in the human lung epithelial cell line 16HBE and delayed TJ formation in p

193 A recombinant human corneal limbal epithelial cell line expressing a LC3-GFP fusion protein

194 ured cells was studied using a human mammary epithelial cell line that expresses SULT1A3 at levels co

195 ed R-loop formation in a normal human breast epithelial cell line when ERalpha was introduced.

196 ed that hypothesis by infecting an oviductal epithelial cell line with C muridarum, followed by immun

197 nd tryptamine toxicity on a human intestinal epithelial cell line.

198 cis-regulatory networks of two human mammary epithelial cell lines (184A1 and MCF10A) are investigate

199 Human cholangiocytes, epithelial cells lining bile ducts, were cultured as pol

200 is an ER stress sensor uniquely expressed in epithelial cells lining mucosal surfaces.

201 human pathogen Chlamydia trachomatis targets epithelial cells lining the genital mucosa.

202 g of cytotoxic T cells to mediate intestinal epithelial cell lysis.

203 at constitutive AKT activation in intestinal epithelial cells markedly enhances tumor invasion and me

204 In epithelial cells, ME spread more efficiently, consistent

205 not GT-I) invaded bovine and murine mammary epithelial cells (MECs) and induced apoptosis, as determ

206 PRRSV-induced autophagy in thymic epithelial cells modulates the development of T cells, a

207 Here we examine medullary thymic epithelial cell (mTEC) heterogeneity and its influence o

208 mediating deletion, namely medullary thymic epithelial cells (mTECs) and dendritic cells, whereas TR

209 asthma pathophysiology, including on airway epithelial cells, mucus hypersecretion, and airway remod

210 Alveolar epithelial cells, myofibroblasts and endothelial cells u

211 methylation and acetylation associated with epithelial cells, NKT, MAIT, TCR-gammadelta, Monocytes,

212 The effect of EtHOBA on mutations in gastric epithelial cells of H pylori-infected INS-GAS mice was a

213 activity was sharply increased in intestinal epithelial cells of microbiota-replete mice compared wit

214 Most paramyxoviruses enter epithelial cells of the airway using sialic acid as a re

215 cells that surround the biliary tree but not epithelial cells of the canals of Hering.

216 the main duct of a portal tract but not the epithelial cells of the ductular reaction, which were in

217 The virus naturally infects epithelial cells of the feather follicle epithelium from

218 uding apical midbody migration in polarizing epithelial cells of the gut, pharynx and sensory neurons

219 nonnephropathogenic strain M41 bound to the epithelial cells of the trachea.

220 Apical domains of epithelial cells often undergo dramatic changes during m

221 Pretreatment of cultured Vero epithelial cells or freshly isolated human nasal epithel

222 ts role has not been investigated in gastric epithelial cells or gastric tumorigenesis.

223 agy gene Atg7 specifically in all intestinal epithelial cells or in Lgr5(+)ISC, we show that loss of

224 issue-specific deletion of VDR in intestinal epithelial cells or myeloid cells.

225 Adhesion to vaginal epithelial cells, pH, D/L-lactate production and lactate

226 specific respiratory, corneal and intestinal epithelial cells, potentially explaining the high effici

227 hypothesized that Chlamydia-infected DCs and epithelial cells present overlapping sets of Chlamydia-M

228 report in Science that type III IFNs disrupt epithelial cell proliferation and differentiation in the

229 ing of E-cadherin and EdU revealed decreased epithelial cell proliferation at the cervical region of

230 d HDM resulted in a significant reduction in epithelial cell proliferation in PSW compared to control

231 Here, we report how epithelial cells recognize and respond to aeroallergen a

232 , HCMV downregulated the expression of nasal epithelial cell-related genes.

233 infection of polarized primary human airway epithelial cells resulted in increased adherence of NTHI

234 arious cell types, including fibroblasts and epithelial cells resulted in the formation of unusually

235 w that ablation of HNF-1beta in mIMCD3 renal epithelial cells results in activation of beta-catenin a

236 In multiple systems examined, epithelial cells round up and move in the apical directi

237 IR-AF) provided evidence for retinal pigment epithelial cell (RPE) involvement.

238 cells and immortalized normal human prostate epithelial cells (RWPE1), but the identity of OLFM4-expr

239 While endocervical epithelial cells secreted large amounts of several cytok

240 Tubular epithelial cells showed strong production of periostin d

241 pithelial cells and immortalized swine nasal epithelial cells (siNEC) and tracheal epithelial cells (

242 nasal epithelial cells (siNEC) and tracheal epithelial cells (siTEC) that retained the abilities to

243 Development, homeostasis, and repair entail epithelial cell size changes driven by mechanical forces

244 Epithelial cells spontaneously form acini (also known as

245 In human primary bronchial epithelial cells ST2 mRNA and protein expression were as

246 f macrophages in obese mice enhanced mammary epithelial cell stem/progenitor activity, elevated expre

247 emonstrate a novel mechanism by which cystic epithelial cells stimulate myofibroblasts in the pericys

248 e marrow chimeras, GILT expression in thymic epithelial cells (TECs), but not hematopoietic cells, wa

249 estinal mucosa is lined by a single layer of epithelial cells that forms a tight barrier, separating

250 ed of a monolayer of diverse and specialized epithelial cells that perform functions ranging from nut

251 ave developed immortalized swine respiratory epithelial cells that retain the ability to differentiat

252 ry mediators) that feed back to regulate the epithelial cells themselves.

253 been shown to stimulate DNA damage in breast epithelial cells through mechanisms mediated by estrogen

254 s able to transform fallopian tube secretory epithelial cells through the inhibition of RB1 and stimu

255 tro exposure of human renal proximal tubular epithelial cells to C5a led to altered mitochondrial res

256 of PCP signaling from polarizing a field of epithelial cells to conferring new properties at subcell

257 quence and RNA sequence from human bronchial epithelial cells to dissect functional genes/SNPs for as

258 ed within photoreceptors and retinal pigment epithelial cells to facilitate retinoid trafficking, to

259 n induced pluripotent stem cell-derived lung epithelial cells to model early-stage lung adenocarcinom

260 ge outlined here demonstrates the ability of epithelial cells to possess highly organized defense mac

261 We then cultured WI-38 fibroblasts and A549 epithelial cells to probe their motile response to the s

262 , the cellular processes and contribution of epithelial cells to the host response are poorly underst

263 ch in turn facilitates the movement of tumor epithelial cells toward nutrient-rich territories.

264 y activating the p62-NRF2 axis, resulting in epithelial cell transformation.

265 gment epithelium (RPE) is a highly polarized epithelial cell type maintained at a senescence state, a

266 mokers, we generate a comprehensive atlas of epithelial cell types and states, connect these into lin

267 Using single-cell transcriptomics, novel epithelial cell types are being unraveled that might pla

268 ution representation of the multiple mammary epithelial cell types in the organoids, and demonstrate

269 We recovered key epithelial cell types including principal cells, clear c

270 ron progenitor cells (NPCs) give rise to all epithelial cell types of the nephron, the filtering unit

271 : Single-cell RNA sequencing was used to map epithelial cell types of the normal and IPF human airway

272 Due to rapid turnover of most epithelial cell types, the cytoplasmic function of YAP1

273 tochondrial respiration in two human mucosal epithelial cell types: insulin-insensitive corneal epith

274 the DeltassrA strain was also abnormal: the epithelial cells underwent premature swelling, and host

275 type and TP53 knockout human retinal pigment epithelial cells using a focused dual guide RNA library

276 econd, when Xist is conditionally deleted in epithelial cells using Keratin14-Cre or in B cells using

277 HSV-1 enters epithelial cells via an endocytosis mechanism that is lo

278 Immortalised vaginal epithelial cells (VK2 E6/E7), modelling the vaginal epit

279 proliferation of normal or tumor intestinal epithelial cells was observed upon genetic inactivation

280 Cellular growth of lens epithelial cells was photo-documented daily.

281 lung microvascular endothelial and alveolar epithelial cells, we demonstrated that N-WASP downregula

282 tion factor TFIIH, in both B lymphocytes and epithelial cells, we hypothesized that SM utilizes XPB t

283 LT also promotes ETEC adhesion to intestinal epithelial cells, we postulated that increases in cAMP,

284 IL-33eGFP + epithelial cells were decreased in Alt Ext challenged Es

285 g to and subsequent infection of respiratory epithelial cells were increased upon preincubation of th

286 Yellow staining of detached pigment epithelial cells were rare.

287 PBMCs from healthy donors and/or respiratory epithelial cells were stimulated with soluble antigens o

288 ity of myelin, and at the apical membrane of epithelial cells, where it has a critical role in transp

289 multiple, dispersed assembly compartments in epithelial cells, which complicates the study of HSV ass

290 ss I and II molecules in endothelial but not epithelial cells, which exhibited constitutive expressio

291 its expression transformed immortalized lung epithelial cells while a transgenic model featuring indu

292 rticipants underwent bronchoscopy to collect epithelial cells whose DNA methylation was measured usin

293 These genes are co-expressed in nasal epithelial cells with genes involved in innate immunity,

294 helial cells or freshly isolated human nasal epithelial cells with low concentrations of sphingosine

295 el: the fusion was faster for spheroids from epithelial cells with lower apparent surface tension tha

296 s of an increase in the number of intestinal epithelial cells with nuclear beta-catenin and SRY-box t

297 T. trichiura larvae moult within intestinal epithelial cells, with adult worms embedded in a partial

298 cation, is found predominantly in intestinal epithelial cells, with chromogranin A-positive enteroend

299 to exert a detrimental effect primarily upon epithelial cells, with corresponding increases in IL8, T

300 ssed predominantly in bronchial and alveolar epithelial cells, with reduced expression in alveolar ep