ライフサイエンスコーパス: chemotactic factor

1 ferred to as T-lymphocyte-derived eosinophil chemotactic factor.

2 chamber assay using PDGF-BB (20 ng/ml) as a chemotactic factor.

3 ive tissue is a principal smooth muscle cell chemotactic factor.

4 ctivator, or the tripeptide fMLP, which is a chemotactic factor.

5 ndependent growth, while serving as a potent chemotactic factor.

6 DEP represents a new class of chemotactic factor.

7 n of major inflammatory cytokines, including chemotactic factors.

8 timulation of HMPS activity or glycolysis by chemotactic factors.

9 ng an activation by Fas ligand of neutrophil chemotactic factors.

10 platelet-activating factor, IL-8, or RANTES chemotactic factors.

11 lar endothelial cell expression of leukocyte chemotactic factors.

12 ctivated by various cytokines, stresses, and chemotactic factors.

13 enhance the respiratory burst in response to chemotactic factors.

14 sue deposition by altering the production of chemotactic factors.

15 pid rafts, leading to expression of monocyte chemotactic factors.

16 from infected rats was used as the source of chemotactic factors.

17 ially and temporally controlled gradients of chemotactic factors.

18 e chemotactic response of neutrophils to the chemotactic factors.

19 also inhibit leukocyte chemotaxis induced by chemotactic factors.

20 t diseases involving leukocyte migration and chemotactic factors.

21 tly induced interleukin-10 (IL-10), monocyte chemotactic factor 1, IL-1beta, and tumor necrosis facto

22 nophil-derived cytokines include JE/monocyte chemotactic factor-1 and TGF-beta1, this cytokine networ

23 factor-alpha and cytokine-induced neutrophil chemotactic factor-1 in plasma were determined by enzyme

24 ta, basic fibroblast growth factor, monocyte chemotactic factor-1, and granulocyte CSF (G-CSF) had no

25 s cases are Ig light chain, AA, or leukocyte chemotactic factor 2 amyloidosis, but rare hereditary fo

26 ability of IGF-I to serve additionally as a chemotactic factor affecting the mobility and invasive p

27 eri generated significantly higher levels of chemotactic factors after 24 h of incubation than did ex

28 hibit a hyperactive phenotype in response to chemotactic factors after cell "priming" with IL-5 famil

29 tion of reactive oxygen species and monocyte chemotactic factors after exposure of adipocytes to satu

30 ines (alveolar macrophage-derived neutrophil chemotactic factor [AMCF]-I/interleukin-8 and AMCF-II).

31 ion revealed that histamine acts as a T cell chemotactic factor and defective T cell trafficking was

32 broblast growth factor 1 (FGF-1) is a potent chemotactic factor and induces tyrosine phosphorylation

33 , cholesterol-containing diet showed reduced chemotactic factor and proinflammatory cytokine expressi

34 infection depends in part upon a gradient of chemotactic factors and adhesion molecules expressed by

35 Positive regulation of cell migration by chemotactic factors and downstream signaling pathways ha

36 contact with fibrinogen, endothelial cells, chemotactic factors and indomethacin, and treatment with

37 Alterations in the levels of chemotactic factors and other proinflammatory cytokines

38 ts the production of MCP-1, a major monocyte chemotactic factor, and either decreases or minimally in

39 due to both the resistance of neutrophils to chemotactic factors, and reduced local production of neu

40 Chemotactic factors are postulated to direct emigration

41 Furthermore, DEK functions as a chemotactic factor, attracting neutrophils, CD8+ T lymph

42 sion of adhesion molecules and production of chemotactic factors, augmenting leukocyte adhesion and r

43 In neural precursors stimulated with the chemotactic factor BDNF, Numb binds to activated TrkB, t

44 r-like growth factor (HB-EGF), a mitogen and chemotactic factor, binds to two receptor tyrosine kinas

45 nt to plastic petri dishes with the purified chemotactic factors C5a and kallikrein increased their r

46 n of Th17 cells and production of neutrophil chemotactic factor CXCL1 in vitro.

47 xes resulted in expression of the neutrophil chemotactic factors CXCL1/KC, CXCL5/LIX, and CXCL8/IL-8.

48 ous PKCalpha increased the production of the chemotactic factors cytokine-induced neutrophil chemoatt

49 rming Growth Factor-beta (TGF-beta), and the chemotactic factor derived from the conditioned culture

50 The chemotactic factors differed for the PMN and J774 cells,

51 Excess glucose and SFAs regulate chemotactic factor expression by a mechanism that involv

52 uitment and activation by inducing leukocyte chemotactic factor expression from VEC.

53 ertain SFAs, but not excess glucose, trigger chemotactic factor expression via a TLR4-dependent pathw

54 ctive oxygen species generation and monocyte chemotactic factor expression.

55 HDL, and methyl-beta-cyclodextrin inhibited chemotactic factor expression.

56 icates that exposure of human neutrophils to chemotactic factor FMLP as well as granulocyte-macrophag

57 the addition of IL-5 family cytokines or the chemotactic factors fMLP, CCL5, and CCL11.

58 to the surface of leukocytes serves as a co-chemotactic factor for C5a, significantly enhancing the

59 Thus, serum levels of IL-16, a key chemotactic factor for CD4(+) lymphocytes, were reduced

60 activity with HER4; and (iii) it is a potent chemotactic factor for cells overexpressing HER4.

61 noate (5-oxoETE) is gaining recognition as a chemotactic factor for eosinophilic (Eo) as well as neut

62 fold), a chemokine initially described as a chemotactic factor for eosinophils.

63 owth factor (HB-EGF) is a potent mitogen and chemotactic factor for fibroblasts, smooth muscle cells

64 c activity by itself; and (iii) it acts as a chemotactic factor for fibroblasts.

65 levated levels of circulating IL-8, a potent chemotactic factor for granulocytes and T lymphocytes, a

66 receptor CXCR3 and is known to function as a chemotactic factor for human T cells, particularly follo

67 -1alpha), is known to function in vitro as a chemotactic factor for lymphocytes, monocytes, and dendr

68 These results suggest that SDF-1 is a potent chemotactic factor for mature MKs.

69 amino-acid chemokine thought to be the major chemotactic factor for monocytes.

70 the delta subclass of chemokines, is a known chemotactic factor for monocytes/macrophages as well as

71 e inflammatory protein 2 (MIP-2), a powerful chemotactic factor for neutrophils which is secreted by

72 Murine (Mu)Mig functioned as a chemotactic factor for resting memory and activated T ce

73 disease that, we show, also acts as a potent chemotactic factor for the migration of these leukocytes

74 strated that IP-10 is a potent mitogenic and chemotactic factor for vascular smooth muscle cells, the

75 blastic and osteocytic cells contain soluble chemotactic factors for bone marrow mesenchymal progenit

76 f chemokines and triggered the production of chemotactic factors for macrophages and neutrophils.

77 is suggests neutrophils may be the source of chemotactic factors for monocytes.

78 Although MLO-Y4 cells secrete potent chemotactic factors for osteoclast precursors, CCL7 was

79 he Trk receptor tyrosine kinases, are potent chemotactic factors for smooth muscle cells, and the exp

80 In vitro, HepG2 cells secreted functional chemotactic factors for tumor-derived lymphocytes that c

81 (CyPA) and CyPB have been well described as chemotactic factors for various leukocyte subsets, sugge

82 lar cyclophilins have been well described as chemotactic factors for various leukocyte subsets.

83 in accordance with tissue gene expression of chemotactic factors, for which receptors are differently

84 siRNA suppressed ROS generation and monocyte chemotactic factor gene expression induced by both gluco

85 ies (ROS) in adipocytes, leading to monocyte chemotactic factor gene expression.

86 ucose-stimulated ROS generation and monocyte chemotactic factor gene expression.

87 ellular spatial information in the form of a chemotactic factor gradient is transduced into intracell

88 e structure of a small-molecule, non-peptide chemotactic factor has been determined from activity pur

89 Unlike chemotactic factors, however, AA was fully active on cel

90 an genes than is porcine alveolar macrophage chemotactic factor-II.

91 capable of migrating toward the CD4-specific chemotactic factor IL-16, providing another function for

92 as TNF-alpha, IL-1 beta, and the neutrophil chemotactic factor IL-8 and inhibitors (e.g., soluble TN

93 lar adhesion molecule-1 [ICAM-1] and soluble chemotactic factors (IL-8).

94 say revealed the presence of a single active chemotactic factor in the supernatant from this incubati

95 d monocytes, indicating that CRAMP acts as a chemotactic factor in vivo.

96 FFAs induce expression of monocyte chemotactic factors in adipocytes via both transcription

97 he PDGFbeta receptor and VSMC sensitivity to chemotactic factors in serum, leading to altered migrato

98 ability of HepG2 cells to secrete lymphocyte chemotactic factors in vitro suggests that the tumor con

99 ncrease in eotaxin, but not other eosinophil chemotactic factors, in bronchoalveolar lavage fluid aft

100 jury and in VSMCs stimulated with growth and chemotactic factors including angiotensin II, basic fibr

101 in reduced expression of numerous macrophage chemotactic factors, including CCL5.

102 anner secreted an array of T cell-recruiting chemotactic factors, including IL-8, macrophage-derived

103 s ERK1/2, we also observed an enhancement of chemotactic factor-induced Akt phosphorylation after IL-

104 ation and vascular permeability in models of chemotactic factor-induced alveolitis.

105 uce HUVEC expression of the potent leukocyte chemotactic factor interleukin-8 (IL-8).

106 several cellular genes, including the potent chemotactic factor interleukin-8 (IL-8).

107 imals as compared to controls, levels of the chemotactic factors interleukin-5, macrophage inflammato

108 The chemokine-like chemotactic factor leukocyte cell-derived chemotaxin 2 (

109 ficant inhibition of synthesis of the potent chemotactic factor leukotriene B4, and that process was

110 ation and renal expression of the neutrophil chemotactic factor macrophage inflammatory protein-2.

111 ha), and eotaxin, but not macrophage-derived chemotactic factor (MDC), than tissues from lymphoid hyp

112 de (ENA-78), and monocyte-derived neutrophil chemotactic factor (MDNCF).

113 duction of TNFalpha and the transcription of chemotactic factors (MIP-2, KC, S100A8/A9), vascular end

114 rotein-linked receptors for lipid or peptide chemotactic factors, neutrophils apparently also can uti

115 ed a receptor by which a non-serum-dependent chemotactic factor (NSCF) produced by C. albicans induce

116 l chemokine that can act either as a soluble chemotactic factor or as a transmembrane-anchored adhesi

117 ion also reduced the production of the mMDSC chemotactic factor osteopontin by tumor cells.

118 fied PDGF AA as the major stromal fibroblast chemotactic factor produced by tumor cells, and demonstr

119 CCL2, MIP-1alpha/CCL3, and RANTES/CCL5), and chemotactic factor receptors (CCR1, CCR2, and CCR5), but

120 onuclear neutrophils (PMNs) are recruited by chemotactic factors released by AMs to produce an intens

121 Chemotactic factors released by infected macrophages are

122 ainst LAM, suggesting that LAM is one of the chemotactic factors released by Mtb-infected alveolar ma

123 ions by preventing neutrophil activation via chemotactic factors released during reperfusion.

124 Local delivery of chemotactic factors represents a novel approach to tissu

125 These responses, similar to those caused by chemotactic factors, resulted from a rise in the number

126 ression and release of an epithelium-derived chemotactic factor(s) for PMN.

127 ed influx suggests the local production of a chemotactic factor(s) such as interleukin-8 (IL-8).

128 In search for chemotactic factor(s) that may mediate transmigration of

129 Chemokines are more than simple chemotactic factors, since they are also implicated in l

130 In contrast, these chemotactic factors stimulate weak or indiscernible ERK

131 vitro and in vivo towards a gradient of the chemotactic factor stromal cell-derived factor-1 (SDF-1)

132 f IL-22 strongly decreased the expression of chemotactic factors such as CCL3 and CXCL3 and of biomar

133 yperalgesia produced by BMSCs required their chemotactic factors such as CCL4 and CCR2, the integrati

134 tivates endothelial cells (EC) to synthesize chemotactic factors, such as interleukin (IL)-8.

135 induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8).

136 oline induce endothelial cells to synthesize chemotactic factors, such as interleukin 8 (IL-8).

137 GRO alpha is an inducible neutrophil chemotactic factor synthesized in inflamed corneal tissu

138 ascular smooth muscle cell (SMC) mitogen and chemotactic factor that is expressed by endothelial cell

139 ctor-like growth factor (HB-EGF) is a potent chemotactic factor that is induced during ischemia/reper

140 een described as an eosinophil and mast cell chemotactic factor that mediates a number of inflammator

141 stream to a site of infection is mediated by chemotactic factors that are often host-derived.

142 evaluate the entire picture of all monocyte chemotactic factors that potentially contribute to adipo

143 hat tumour hypoxia induces the expression of chemotactic factors that promote tolerance.

144 n of complement and generation of complement chemotactic factors that rapidly recruit macrophages.

145 secretion by cancer cells of proinflammatory chemotactic factors that recruit antitumor effector T ce

146 In this study, it is shown that a classic chemotactic factor, the bacterial chemotactic peptide N-

147 chemotactic response by preincubation with a chemotactic factor to achieve deactivation, 5 x 10(-7) M

148 The capacity of a chemotactic factor to stimulate glucose metabolism of hu

149 Interleukin (IL)-15 is a chemotactic factor to T cells.

150 Apoptotic cells secrete chemotactic factors to attract phagocytic cells, and we

151 The first chemotactic factors to be structurally defined were the

152 During stimulation with fMLP, a chemotactic factor, two Ca2+ waves traveling in opposite

153 es eosinophil responsiveness to a variety of chemotactic factors via a process called priming, althou

154 AC induces macrophage production of multiple chemotactic factors via NF-kappaB to promote monocyte mi

155 The chemotactic factor was concentrated by solid phase chrom

156 ic mAbs indicated that the serotonin-induced chemotactic factor was the previously characterized lymp

157 The release of chemotactic factors was dose dependent and was initiated

158 lthough interleukin-6 (IL-6) is not itself a chemotactic factor, we found that medium from il-6-/- ne

159 Six monocyte chemotactic factors were found to be predominantly upreg

160 g clear that there is a complex interplay of chemotactic factors, which changes over time as the infl

161 ction in direct response to locally produced chemotactic factors, which signal through specific G pro