2019
DOI: 10.1016/j.celrep.2019.03.074
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The Exchangeable Apolipoprotein Nplp2 Sustains Lipid Flow and Heat Acclimation in Drosophila

Abstract: Highlights d We identified Nplp2, an exchangeable apolipoprotein in Drosophila d Nplp2 maximizes Lipophorin lipid loading capacity d Nplp2 controls dietary lipid extraction and optimal fat storage d Nplp2 fuels the stress response with dietary lipids and promotes heat acclimation

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Cited by 19 publications
(16 citation statements)
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“…The PL‐vir1 cluster contains 4.5% of the total hemocytes and expresses the same strong markers as PL‐Rel, including Rel, Jra, and Puc (Fig D, Dataset EV2). Compared to PL‐Rel, however, the marker of viral infection Vir1 (Dostert et al , ), the protein Pastrel involved in resistance to virus infection (Magwire et al , ; Martins et al , ), the predicted peptidase Ance‐5, and the apolipoprotein Nplp2 (Rommelaere et al , ) are all up‐regulated. PL‐vir1 also presents the same GO terms as PL‐Rel, with respect to the defense response to bacterium and to the Toll signaling pathway (Fig C).…”
Section: Resultsmentioning
confidence: 99%
“…The PL‐vir1 cluster contains 4.5% of the total hemocytes and expresses the same strong markers as PL‐Rel, including Rel, Jra, and Puc (Fig D, Dataset EV2). Compared to PL‐Rel, however, the marker of viral infection Vir1 (Dostert et al , ), the protein Pastrel involved in resistance to virus infection (Magwire et al , ; Martins et al , ), the predicted peptidase Ance‐5, and the apolipoprotein Nplp2 (Rommelaere et al , ) are all up‐regulated. PL‐vir1 also presents the same GO terms as PL‐Rel, with respect to the defense response to bacterium and to the Toll signaling pathway (Fig C).…”
Section: Resultsmentioning
confidence: 99%
“…2b). We scored highly enriched genes in the potential intermediate subclusters and noticed that expression of Nplp2, a novel apolipoprotein 38 , peaks at PH4, GST-rich, PM1, and CC1 and is lower in other subclusters (Fig. 2b).…”
Section: Resultsmentioning
confidence: 99%
“…Gut hormones also play key roles in metabolic adaptations and signal to a diverse set of target organs. Genetic, transcriptomic, and immunohistochemical evidence suggests that larval or adult midgut enteroendocrine cells express *AstA, *Allatostatin C (AstC), BursA, *CCHa1, *CCHa2, CNMamide (CNMa), Crustacean cardioactive peptide (CCAP), *Diuretic hormone 31 (Dh31), Ion-transport peptide (ITP), *Myoinhibitory peptide/Allatostatin B (MIP), Neuropeptide F (NPF), Neuropeptide-like precursor 2 (NPLP2, likely functioning as an apolipoprotein rather than, or in addition to, as a prepropeptide [190]), Orcokinin, *sNPF, and *Tachykinin (Tk), expressed in stereotyped combinations and anatomical regions [191][192][193][194][195][196][197]. However, without evidence of proper peptide processing and release, prepropeptide expression alone is insufficient to prove biological activity.…”
Section: Signals That Regulate the Ipcsmentioning
confidence: 99%