ライフサイエンスコーパス: pinocytosis

1 or of actin assembly, cell polarization, and pinocytosis.

2 d-phase pinocytosis or inducible fluid-phase pinocytosis.

3 delivered by DEC205-mediated endocytosis and pinocytosis.

4 tosis and the documented dynamin-independent pinocytosis.

5 serum treatment appeared to be the result of pinocytosis.

6 hilic leukemia cells and in cells performing pinocytosis.

7 ysiological downregulation of dendritic cell pinocytosis.

8 GF-induced membrane ruffling and fluid phase pinocytosis.

9 unaffected by inhibitors of endocytosis and pinocytosis.

10 timulates cell surface membrane ruffling and pinocytosis.

11 s as they are internalized into endosomes by pinocytosis.

12 either through these pores or by reparative pinocytosis.

13 dicated by the ability of v-Abl to stimulate pinocytosis.

14 isceral yolk sac cells, suggesting uptake by pinocytosis.

15 omitant reduction in the rate of fluid phase pinocytosis, a significant decrease in the efficiency of

16 rophages that show high rates of fluid-phase pinocytosis also show similar high rates of uptake of na

17 t cross the plasma membrane, utilizing fluid pinocytosis and a specific lysosomal transporter.

18 Together, these data suggest that pinocytosis and adhesion are raft-dependent functions in

19 vitelline fluid is initially internalized by pinocytosis and degraded by lysosomes; in later stages,

20 ortmannin and LY294002 inhibited fluid-phase pinocytosis and Fc receptor-mediated phagocytosis, but t

21 ke up LDL-sized nanoparticles by fluid-phase pinocytosis and indicate that fluid-phase pinocytosis of

22 IL-4 and IL-13 enhanced fluid phase pinocytosis and mannose receptor-mediated uptake by acti

23 L-10 or IFN-gamma decreased both fluid phase pinocytosis and mannose receptor-mediated uptake.

24 Pinocytosis and membrane ruffling are among the earliest

25 ne proteins and that SP-D enhances efficient pinocytosis and phagocytosis of DNA by macrophages and m

26 gregated LDL taken up by macrophages through pinocytosis and phagocytosis, respectively, aggregated L

27 the cell, and it has been shown to regulate pinocytosis and phagocytosis; however, its effects on po

28 as(G12V) separately activates Rab5-dependent pinocytosis and Rac1-dependent membrane ruffling.

29 ed CDG greatly enhances Ag uptake, including pinocytosis and receptor-mediated endocytosis in vivo.

30 we measured internalization of gelonin (via pinocytosis) and gelonin-based immunotoxins (via antigen

31 l important virulence functions, fluid-phase pinocytosis, and adhesion to host cell monolayers.

32 ative regulator of cell growth, cytokinesis, pinocytosis, and phagocytosis, as all are enhanced in co

33 e trafficking events including phagocytosis, pinocytosis, and transferrin receptor recycling were als

34 stimulation, was independent of endocytosis/pinocytosis, and was consistent with bidirectional, tran

35 tudy demonstrates that membrane ruffling and pinocytosis are regulated by distinct Ras signal transdu

36 mined that the mutant strain was impaired in pinocytosis but normal in phagocytosis of beads or bacte

37 The Ha-Ras(G12V)-stimulated pinocytosis but not membrane ruffling was abolished by e

38 cs the stimulatory effect of Ha-Ras(G12V) on pinocytosis but not membrane ruffling.

39 Cytochalasin B, which inhibited pinocytosis by 65% and phagocytosis by 93%, decreased ed

40 than that achieved previously by nonspecific pinocytosis, CBATP mediates time-, temperature- and conc

41 ied LDL by receptor-independent, fluid-phase pinocytosis converting these macrophages into foam cells

42 also taken up by cells in a temperature- and pinocytosis-dependent manner.

43 iameter beads, which can enter cells through pinocytosis, did not stimulate IL-12 expression.

44 ond, we found that CDG selectively activated pinocytosis-efficient-DCs, leading to T(H) polarizing cy

45 tive LDL by receptor-independent fluid-phase pinocytosis, either constitutively or in response to spe

46 -based behaviors that were tested, including pinocytosis, exocytosis, cytokinesis and morphogenesis,

47 eptor-mediated endocytosis and non-saturable pinocytosis for uptake of the conjugate.

48 Fluid-phase pinocytosis has been demonstrated by macrophages within

49 serve as models of LDL uptake by fluid-phase pinocytosis in cultured human monocyte-derived macrophag

50 amily of GTPases are involved in and control pinocytosis in dendritic cells.

51 The mechanisms of regulation of fluid-phase pinocytosis in macrophages and, specifically, the role o

52 SH2 domain, inhibited membrane ruffling and pinocytosis induced by GH and PDGF.

53 ed phagocytosis by >90% but had no effect on pinocytosis, inhibited edge cell liposome-DNA complex en

54 eptide transporter, and (iii) was blocked by pinocytosis inhibitors but not by brefeldin A.

55 oes not affect cell growth, phagocytosis, or pinocytosis, inhibits the formation of head-to-tail cell

56 phagocytosis, but not the receptor-mediated pinocytosis, is highly associated with the production of

57 fore sought to determine whether fluid-phase pinocytosis occurs in vivo in macrophages in atheroscler

58 ibited receptor-mediated endocytosis of LDL, pinocytosis of 10-nm microspheres, and phagocytosis of 2

59 overexpression, wortmannin abolished amebic pinocytosis of dextrans but had no inhibitory effects on

60 defective in capping and cytokinesis, while pinocytosis of fluorescent dextrans was not affected.

61 Fluid-phase pinocytosis of LDL by macrophages is regarded as a novel

62 se pinocytosis and indicate that fluid-phase pinocytosis of LDL is a mechanism for macrophage foam ce

63 s on an SP-A substrate demonstrated enhanced pinocytosis of mannose BSA and phagocytosis of Mycobacte

64 s not necessary for MR up-regulation, and 3) pinocytosis of mannose BSA via MR recycling was increase

65 , but degradation of internalized ligand and pinocytosis of the fluid-phase marker Lucifer Yellow wer

66 endocytosis, but not by compounds that block pinocytosis or cellular entry via scavenger or mannose r

67 demonstrate either constitutive fluid-phase pinocytosis or inducible fluid-phase pinocytosis.

68 cated by possible uptake through fluid-phase pinocytosis or membranous ducts.

69 HDMEC are similar to HUVEC in rates of pinocytosis or receptor-mediated endocytosis.

70 is internalized by a relatively nonspecific pinocytosis or transcytosis mechanism.

71 monocytes by receptor-mediated endocytosis, pinocytosis, or phagocytosis and measured internalizatio

72 is protein is not essential for cytokinesis, pinocytosis, phagocytosis, or development.

73 of wild-type SH2-Bbeta enhanced ruffling and pinocytosis produced by submaximal GH but not submaximal

74 mediated by phagocytosis and endocytosis or pinocytosis, respectively.

75 Thus, targeting macrophage fluid-phase pinocytosis should be considered when investigating stra

76 and was specific for endocytosis rather than pinocytosis since a TR mutant lacking an internalization

77 readouts: induction of membrane ruffling and pinocytosis, stimulation of cell motility, and Pak bindi

78 d Rac on plasma membrane morphology and bulk pinocytosis, there has been no evidence for their involv

79 to that by which Ags taken up by fluid phase pinocytosis traffick, suggesting that the accelerated BC

80 ve to control Ax2 cells, whereas fluid-phase pinocytosis was reduced threefold, primarily as the resu

81 nd activated Rho has been shown to stimulate pinocytosis when microinjected into Xenopus oocytes.

82 hosphatase inhibitor reduces Cdc42-regulated pinocytosis while stimulating caveolar endocytosis.