ライフサイエンスコーパス: oenocyte

1 ialized for lipid metabolism (fat bodies and oenocytes).

2 iate number of lipid-processing cells called oenocytes.

3 of an abdomen-specific cell fate: the larval oenocytes.

4 , neurons in the larval and adult brain, and oenocytes.

5 mammalian liver are performed in insects by oenocytes.

6 m: chordotonal sensory organs and non-neural oenocytes.

7 ets the binary cell-fate switch in favour of oenocytes.

8 cle but in the sub-epdiermal hepatocyte-like oenocytes.

9 Thus, in order to make an oenocyte, abdA regulates just one principal target, rho,

10 gulator and the Brummer lipase indicate that oenocytes act downstream of the fat body.

11 Garland cells and oenocytes (also called Drosophila nephrocytes) function

12 pecific loss of tracheal expression, leaving oenocyte and midline glia expression intact.

13 bset of abdominal SOP cells to induce larval oenocytes and showed that RhoBAD is regulated by an Abdo

14 Autotoxins are synthesised by oenocytes and some of them correspond to alkene hydrocar

15 of future research include the evolution of oenocytes and their cross talk with other tissues involv

16 most prominent expression in adult fat body, oenocytes, and the basolateral region of midgut cells an

17 t, in both short and long germ-band species, oenocytes are induced from a Spalt major/Engrailed ectod

18 bolium castaneum support the hypothesis that oenocytes are of ectodermal origin.

19 In turn, oenocytes are required for depleting stored lipid from t

20 Here we identify the oenocyte as the principal cell type accumulating lipid d

21 ctive activation of insulin/IGF signaling in oenocytes by a fat body-derived peptide represents a pre

22 methyl-Z7-octadecene, is most likely made in oenocyte cells associated with abdominal epidermal cells

23 tissues: the lymph glands, Garland cells and oenocyte cells, which are all specialized tissues in whi

24 d that expression of mFAS is undetectable in oenocytes (cells that produce CHCs) of a closely related

25 is identified as a critical component of the oenocyte/chordotonal fate switch.

26 midline glias of the ventral nerve cord, the oenocyte clusters, and all tracheal cells.

27 Oenocyte-directed RNAi knock-down of Drosophila CYP4G1 o

28 te that the SAL zinc-finger protein promotes oenocyte formation and supresses chordotonal organ induc

29 also required for proper RhoBAD activity and oenocyte formation.

30 When food is plentiful, oenocytes have critical roles in regulating growth, deve

31 Oenocytes have intrigued insect physiologists since the

32 ecific expression profiling, we confirm that oenocytes in adult flies play a central role in the meta

33 ased levels of lipid metabolites produced by oenocytes in spin mutants allude to a functional interac

34 ward oenocyte-less flies is attributed to an oenocyte-independent sustained production of the Or47b l

35 into some of the physiological functions of oenocytes indicate that they involve fatty acid and hydr

36 -metabolic coupling between the fat body and oenocytes is bidirectional.

37 the vigorous male courtship displayed toward oenocyte-less flies is attributed to an oenocyte-indepen

38 ulate rhomboid CRM activity to induce proper oenocyte numbers.

39 ecessary but not sufficient component of the oenocyte prepattern that also serves to raise the appare

40 ed for tracheal waterproofing and that adult oenocytes produce cuticular hydrocarbons required for de

41 ke peptide 6 (dILP6) induces lipid uptake in oenocytes, promoting lipid turnover during fasting and i

42 id accumulation in the midgut, fat body, and oenocytes (specialized hepatocyte-like cells) and decrea

43 SAL upregulation is triggered as part of the oenocyte-specific EGFR response.

44 Together, our results suggest that the oenocyte-specific LmCYP4G102 plays a critical role in th

45 es in D. melanogaster have shown that larval oenocytes synthesize very-long-chain fatty acids require

46 eraction between the fat body and liver-like oenocytes that regulates the mobilization of lipid store

47 h CYP4G16 and CYP4G17 are highly abundant in oenocytes, the insect cell type thought to secrete hydro

48 antly expressed in the fat body, midgut, and oenocytes: the principal sites of intermediary metabolis

49 We focus on the larval oenocyte, which is restricted to the abdomen and induced