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1 ialized for lipid metabolism (fat bodies and oenocytes).
2 flammation, specifically in fly hepatocytes (oenocytes).
3 cle but in the sub-epdiermal hepatocyte-like oenocytes.
4 g the Pi3K/Akt1/TOR signaling cascade in the oenocytes.
5 iate number of lipid-processing cells called oenocytes.
6 of an abdomen-specific cell fate: the larval oenocytes.
7 , neurons in the larval and adult brain, and oenocytes.
8  mammalian liver are performed in insects by oenocytes.
9 m: chordotonal sensory organs and non-neural oenocytes.
10 al import and elevated JNK signaling in aged oenocytes.
11 ets the binary cell-fate switch in favour of oenocytes.
12 t upd3 is significantly up-regulated in aged oenocytes.
13                    Thus, in order to make an oenocyte, abdA regulates just one principal target, rho,
14 lar to the mammalian hepatocytes, Drosophila oenocytes accumulate fat during fasting, but it is uncle
15 gulator and the Brummer lipase indicate that oenocytes act downstream of the fat body.
16  of the DsFAR2-B ortholog in D. melanogaster oenocytes affected CHCs in a similar way to that seen in
17                            Garland cells and oenocytes (also called Drosophila nephrocytes) function
18 pecific loss of tracheal expression, leaving oenocyte and midline glia expression intact.
19 bset of abdominal SOP cells to induce larval oenocytes and showed that RhoBAD is regulated by an Abdo
20                Autotoxins are synthesised by oenocytes and some of them correspond to alkene hydrocar
21 at1 in maintaining the proper functioning of oenocytes and the central role of oenocytes in the regul
22  of future research include the evolution of oenocytes and their cross talk with other tissues involv
23 most prominent expression in adult fat body, oenocytes, and the basolateral region of midgut cells an
24 t, in both short and long germ-band species, oenocytes are induced from a Spalt major/Engrailed ectod
25 bolium castaneum support the hypothesis that oenocytes are of ectodermal origin.
26                                     In turn, oenocytes are required for depleting stored lipid from t
27                         Here we identify the oenocyte as the principal cell type accumulating lipid d
28 ctive activation of insulin/IGF signaling in oenocytes by a fat body-derived peptide represents a pre
29 methyl-Z7-octadecene, is most likely made in oenocyte cells associated with abdominal epidermal cells
30 ductase gene, DsFAR2-B, that is expressed in oenocyte cells where CHCs are synthesized.
31 tissues: the lymph glands, Garland cells and oenocyte cells, which are all specialized tissues in whi
32 d that expression of mFAS is undetectable in oenocytes (cells that produce CHCs) of a closely related
33 is identified as a critical component of the oenocyte/chordotonal fate switch.
34 midline glias of the ventral nerve cord, the oenocyte clusters, and all tracheal cells.
35                                              Oenocyte-directed RNAi knock-down of Drosophila CYP4G1 o
36                     Fru or Hnf4 depletion in oenocytes disrupts lipid homeostasis, resulting in a sex
37 t ImpL2 (IGFBP7 in mammals) is secreted from oenocytes during starvation in a Desat1-dependent manner
38 or pheromone biosynthesis in hepatocyte-like oenocytes for sexual attraction.
39 te that the SAL zinc-finger protein promotes oenocyte formation and supresses chordotonal organ induc
40 also required for proper RhoBAD activity and oenocyte formation.
41                      When food is plentiful, oenocytes have critical roles in regulating growth, deve
42                                              Oenocytes have intrigued insect physiologists since the
43  of cytokine unpaired 3 (upd3) in Drosophila oenocytes (hepatocyte-like cells) is the primary non-aut
44 ecific expression profiling, we confirm that oenocytes in adult flies play a central role in the meta
45 ased levels of lipid metabolites produced by oenocytes in spin mutants allude to a functional interac
46                 DBLOX is highly expressed in oenocytes in the fat-body tissue, and these cells increa
47 tioning of oenocytes and the central role of oenocytes in the regulation of fat body lipid metabolism
48 ward oenocyte-less flies is attributed to an oenocyte-independent sustained production of the Or47b l
49  into some of the physiological functions of oenocytes indicate that they involve fatty acid and hydr
50 verexpression is restricted to the midgut or oenocytes, indicating that neither tissue is involved in
51 -metabolic coupling between the fat body and oenocytes is bidirectional.
52 se, Desat1 (SCD in mammals), specifically in oenocytes leads to more saturated lipids in the hemolymp
53 the vigorous male courtship displayed toward oenocyte-less flies is attributed to an oenocyte-indepen
54                              We propose that oenocytes may function as a population of cells that are
55 s also essential for a sustained increase in oenocyte numbers, HDF synthesis, and immune priming.
56 ulate rhomboid CRM activity to induce proper oenocyte numbers.
57 ecessary but not sufficient component of the oenocyte prepattern that also serves to raise the appare
58 ed for tracheal waterproofing and that adult oenocytes produce cuticular hydrocarbons required for de
59 ke peptide 6 (dILP6) induces lipid uptake in oenocytes, promoting lipid turnover during fasting and i
60 rapidly during this stage and that muscle-to-oenocyte Pvf1 signaling inhibits expansion of adipose ti
61                          Loss of Fru(COM) in oenocytes resulted in adults with reduced levels of cuti
62 id accumulation in the midgut, fat body, and oenocytes (specialized hepatocyte-like cells) and decrea
63 SAL upregulation is triggered as part of the oenocyte-specific EGFR response.
64                                   Flies with oenocyte-specific knockdown and overexpression of ImpL2
65                                              Oenocyte-specific knockdown of upd3 is sufficient to blo
66       Together, our results suggest that the oenocyte-specific LmCYP4G102 plays a critical role in th
67                                Intriguingly, oenocyte-specific overexpression of Pex5, the key peroxi
68                 Notably, time-restricted and oenocyte-specific silencing of Relish (an NF-kappaB homo
69 es in D. melanogaster have shown that larval oenocytes synthesize very-long-chain fatty acids require
70 re synthesised in sub-epidermal cells called oenocytes that are very difficult to isolate from surrou
71 eraction between the fat body and liver-like oenocytes that regulates the mobilization of lipid store
72 h CYP4G16 and CYP4G17 are highly abundant in oenocytes, the insect cell type thought to secrete hydro
73 antly expressed in the fat body, midgut, and oenocytes: the principal sites of intermediary metabolis
74 e utilise a transgenic line with fluorescent oenocytes to purify these cells for the first time.
75 nals to the Drosophila hepatocyte-like cells/oenocytes to suppress lipid synthesis by activating the
76                       We focus on the larval oenocyte, which is restricted to the abdomen and induced
77 al effects are localized to the fat body and oenocytes, which perform liver-like functions in insects