ライフサイエンスコーパス: endfeet

1 ion in astrocyte free Ca(2+) in the soma and endfeet.

2 eptors, and form aquaporin-4(+) perivascular endfeet.

3 of GLT-1 were also detected at perivascular endfeet.

4 both astrocytic cell bodies and perivascular endfeet.

5 nts, and pedicles, as well as to Muller cell endfeet.

6 PR56 is present in abundance in radial glial endfeet.

7 in the immediate vicinity of the glial cell endfeet.

8 microtubule-based transport, accumulating in endfeet.

9 , are less prominently concentrated in their endfeet.

10 gulator Cdc42 in radial glia regulates glial endfeet activities and inter-radial glial interactions.

11 er of dystrophin-associated protein in glial endfeet and a rare example of a glial protein with a rol

12 tion induced calcium transients in astrocyte endfeet and an associated dilation of upstream arteriole

13 etween TRPV4 channels and IP3Rs in astrocyte endfeet and demonstrate that TRPV4 channels are engaged

14 nteractions are mediated by growth cone-like endfeet and filopodia-like protrusions.

15 local TRPV4-mediated Ca(2+) oscillations in endfeet and further found that TRPV4 Ca(2+) signals are

16 s communicate with the adjacent radial glial endfeet and influence cortical development.

17 de of spontaneous Ca(2+) events in astrocyte endfeet and inversion of NVC from vasodilation to vasoco

18 pe mice, Kir4.1 is highly clustered in their endfeet and perivascular processes.

19 .1 was present and localized to the proximal endfeet and perivascular processes.

20 E-like immunoreactivity was localized to the endfeet and terminal process of Sus cells surrounding th

21 ward rectifying K(+) channel Kir4.1 at glial endfeet and that disruption of dystrophin and potassium

22 t membrane (BM) located between radial glial endfeet and the meninges during embryonic cerebellar dev

23 We further show that radial glial endfeet are required for the basement-membrane anchoring

24 oepithelial endfeet demonstrating that these endfeet are the preferred site of basal lamina assembly.

25 a in dorsomedial cortex retract their apical endfeet at midneurogenesis and translocate to the overla

26 ayer of the retina and then spread into cell endfeet at the inner retinal surface.

27 KAB-2), which is highly concentrated at the endfeet at the vitreal border and to processes envelopin

28 pecific Cre-mediated recombination disrupted endfeet BMs and led to hemorrhage in deep brain regions

29 We found no evidence of observable astrocyte endfeet Ca(2+) elevations following physiological visual

30 Astrocyte endfeet contacted the monolayer of BMVEC that formed tig

31 ion results in Ca(2+) increases in the glial endfeet contacting capillaries, but not arterioles, and

32 Astrocytic endfeet cover the entire cerebral vasculature and serve

33 tituting along the retracted neuroepithelial endfeet demonstrating that these endfeet are the preferr

34 e lateral membrane domain in the ventricular endfeet during interphase, mPar3 becomes dispersed and s

35 responsive to K(+) released from astrocytic endfeet during NVC, leading to impairment of this proces

36 Photolysis of caged Ca(2+) in astrocytic endfeet ensheathing the vessel wall was associated with

37 Astrocytic endfeet exhibited large-conductance, Ca2+-sensitive K+ (

38 scopy indicated that a similar proportion of endfeet exhibiting eHACSs also exhibited asymmetrical en

39 Here we show that the apical endfeet express high levels of the adhesion and signalin

40 m channel (Kir), whereas the vessel-adjacent endfeet express Kir and BK potassium channels.

41 atter contains radial processes with subpial endfeet expressing vimentin (Vim).

42 ter and Kir4.1 potassium channels from glial endfeet, formation of intracellular vacuoles in alpha-DB

43 of preexisting vessels, displace astrocytic endfeet from endothelial or vascular smooth muscle cells

44 paration to mechanically isolate radial glia endfeet from the soma, and we use photoconvertible prote

45 (eHACSs) after SAH that were not observed in endfeet from unoperated animals.

46 lium, extending long basal processes to form endfeet hundreds of micrometers away from the soma.

47 mon with the glia limitans that is formed by endfeet in other cortical areas.

48 e B cells are anchored by specialized apical endfeet in the center of a pinwheel of ependymal cells.

49 tigated the coverage of vessels by astrocyte endfeet in the prefrontal cortex in MDD.

50 of radial glia and is concentrated at their endfeet in the stratum opticum, at the time retinal axon

51 The clustering of GLT-1 at astrocyte endfeet indicates that it might serve a specialized func

52 our understanding of how basal processes and endfeet influence neurogenesis.

53 n-associated protein scaffolds in astrocytic endfeet, is essential for the formation and functioning

54 ith) mice display detachment of radial glial endfeet, marginal zone heterotopias, and cortical dyslam

55 de that cytoskeletal and signaling events at endfeet may be controlled through translation of specifi

56 )-sensitive potassium channels in astrocytic endfeet mediated a majority of the dilation and the enti

57 expression is markedly reduced in astrocyte endfeet membranes adjacent to blood vessels in cerebellu

58 Retraction of radial glial endfeet, midline fusion of brain hemispheres, and gliosi

59 ane (BM), abnormal anchorage of radial glial endfeet, mislocalized Cajal-Retzius cells, and neuronal

60 The coverage of blood vessels by endfeet of AQP4-immunoreactive (IR) astrocytes was signi

61 on in capillary endothelial cells and in the endfeet of capillary astrocytes, which suggests decrease

62 SARA is enriched at the apical endfeet of radial glia of the neocortex.

63 l studies confirmed that the cell bodies and endfeet of Sus cells expressed high levels of apoE.

64 s, such as an irreversible retraction of the endfeet of the neuroepithelial cells from the vitreal su

65 by cellular receptor proteins on the vitreal endfeet of the retinal neuroepithelial cells.

66 ainly localized to Muller cell processes and endfeet, photoreceptor terminals, and photoreceptor oute

67 atory substances from perivascular astrocyte endfeet, resulting in improved local blood flow.

68 composed of endothelial cells and astrocyte endfeet separated by a basal lamina at their interface.

69 godendrocytes surrounding axons to astrocyte endfeet surrounding capillaries, the proposed panglial s

70 active agents (e.g., K(+)) from perivascular endfeet surrounding parenchymal arterioles.

71 l cells in the brain with fine processes and endfeet that intimately contact both neuronal synapses a

72 es and capillaries, where they terminate in "endfeet" that encase the blood vessels.

73 cellular acidification measured beneath cell endfeet was 304% of the amplitude of the acidification b

74 munoprecipitation and microarray analyses of endfeet, we discover FMRP-bound transcripts, which encod

75 Additionally, astrocytic endfeet were hypertrophic and lacked appropriately polar

76 water homeostasis in perivascular astrocyte endfeet where it is concentrated.

77 eptide colocalizes in perivascular astrocyte endfeet where the 32 kDa polypeptide is abundantly expre

78 al processes and is localized to radial glia endfeet, whereas vimentin mRNA is not localized in radia

79 s of N-cadherin concentrations at the apical endfeet, which can be partially restored by forced Yap e

80 Radial glial endfeet, which comprise glia limitans, grew out of the n

81 d assemble basement membranes (BMs) at their endfeet, which ensheath the cerebrovasculature.

82 itin mRNA is highly localized to radial glia endfeet, which is suggestive of its transport in these c

83 glial network as mature astrocytes that form endfeet with blood vessels, couple electrically to neigh

84 Furthermore, the percentage of endfeet with eHACSs varied with time and paralleled the

85 Endfeet with eHACSs were present only around arterioles

86 enclosing numerous fibroblast and astrocyte endfeet, with pouches of collagen fibrils at the interfa