ライフサイエンスコーパス: coelomocyte

1 -striated muscles, and two non-muscle cells (coelomocytes).

2 es an ion-channel involved in endocytosis by coelomocytes.

3 st and generation of ectopic body muscle and coelomocytes.

4 s, including pharynx cells, body muscles and coelomocytes.

5 of striated body wall muscles and non-muscle coelomocytes.

6 ostendocytic trafficking in both neurons and coelomocytes.

7 containing four types of immunocytes called coelomocytes.

8 isplay TTR.4 fluorescence in macrophage-like coelomocytes.

9 nsible for the closure of lamellar wounds in coelomocytes.

10 ds in the peripheral cytoplasm of sea urchin coelomocytes.

11 muscle cells is endocytosed and degraded by coelomocytes.

12 exity in molecules expressed by invertebrate coelomocytes.

13 of intestinal cells, in spermathecae, and in coelomocytes.

14 are 5.5 kb and are specifically expressed in coelomocytes.

15 f NLP-7 and genes involved in endocytosis by coelomocytes also specifically shorten the life span of

16 cripts of all five OLF family members are in coelomocytes and adult radial nerve tissue.

17 and peripheral blood mononuclear cells), the coelomocytes and differentiated (macrophage-like) THP-1

18 xicity of dissolved silver salt on earthworm coelomocytes and human cells (THP-1 cells, differentiate

19 otein is expressed exclusively in muscle and coelomocytes and localizes to the postsynaptic surface o

20 following the onset of AgNP exposure in the coelomocytes and THP-1 cells.

21 oles in fate specification of sex myoblasts, coelomocytes, and multiple neuronal lineages in C. elega

22 pathways, NLP-7 signaling and endocytosis by coelomocytes, are required for life extension under diet

23 tion of the non-muscle mesodermal cells, the coelomocytes (CCs).

24 n cloned and sequenced from an LPS-activated coelomocyte cDNA library from the purple sea urchin, Str

25 no acids, respectively, were isolated from a coelomocyte cDNA library.

26 cts downstream of mls-2 to specify M-derived coelomocyte cell fates.

27 defects in endocytosis in the intestine and coelomocyte cells.

28 hibition of the Arp2/3 complex in sea urchin coelomocytes, cells that possess an unusually broad LP r

29 ty along the anterior-posterior axis, and 3) coelomocyte competence factor(s).

30 e bacteria resulted in a typical increase in coelomocyte concentration within 24 h, which included an

31 Coelomocytes contain a dense cortical actin network, whi

32 cursor cell fate decision and a sex myoblast/coelomocyte decision, but cannot suppress defects in two

33 es, including tube foot and intestine, or in coelomocytes, despite the presence of SpFGFR transcripts

34 fficient endocytosis of fluids by C. elegans coelomocytes, encodes a protein that is homologous to li

35 hree C. elegans MTMs play essential roles in coelomocyte endocytosis, a process that also requires VP

36 rme-8 mutant coelomocytes fail to accumulate visible quantities of en

37 Amassin-1 mediates intercellular adhesion of coelomocytes (immunocytes).

38 analysis revealed that AML-1 is expressed by coelomocytes in the nephridium and in round cells in the

39 coelomic GFP, indicating that endocytosis by coelomocytes is not essential for growth or survival of

40 made visible by Arp2/3 complex inhibition in coelomocytes may represent an exaggerated manifestation

41 rray hybridizations with repeated samples of coelomocyte messages revealed substantial alterations in

42 we have isolated a set of mutants that alter coelomocyte numbers.

43 body cavity, a massive cell-cell adhesion of coelomocytes occurs.

44 The coelomocytes of Caenorhabditis elegans are scavenger cel

45 te localization and block endocytosis in the coelomocytes of Caenorhabditis elegans.

46 composition for nanoparticle recognition by coelomocytes of the earthworm Eisenia fetida using E. fe

47 Using the six macrophage-like coelomocytes of the nematode Caenorhabditis elegans as a

48 In coelomocytes, postendocytic trafficking of the marker Te

49 Intracellular accumulation of AgNPs in the coelomocytes, predominantly in a phagocytic population,

50 Endocytosis markers taken up by the coelomocytes rapidly accumulate in these large RME-8-pos

51 Sea urchin coelomocytes represent an excellent experimental model s

52 We show that toxin-mediated ablation of coelomocytes results in viable animals that fail to endo

53 In the macrophage-like coelomocytes, RME-8 localizes to the limiting membrane o

54 The mutant has coelomocyte-specific defects without changes in other li

55 Coelomocytes, the heterogeneous population of sea urchin

56 arge disulfide-bonded aggregates that adhere coelomocytes to each other.

57 nce materials) and compared the responses of coelomocytes to protein coronas preformed of EfCP or FBS

58 enol from PVC or sand reduced the ability of coelomocytes to remove pathogenic bacteria by >60%.

59 Coelomocytes transcribe multiple SRCR genes from among a

60 RNAi for other known endocytosis genes, for coelomocyte uptake defective (Cup) phenotypes.

61 -IV) homolog, the recently identified cup-5 (coelomocyte-uptake defective) gene.

62 A general feature of the CK666 phenotype in coelomocytes was transverse actin arcs, and arc generati

63 naturally large endosomes of the C. elegans coelomocyte, we visualized complementary ESCRT-0 and RME

64 some of the genes expressed in LPS-activated coelomocytes, we sequenced randomly chosen clones from a

65 Phagocyte fractions enriched from coelomocytes were used in limiting dilutions to obtain s

66 b, and the gene is expressed specifically in coelomocytes, which are the immunocytes in the sea urchi