Grasshopper Lazarillo, a GPI-anchored Lipocalin, increases Drosophila longevity and stress resistance, and functionally replaces its secreted homolog NLaz

被引:19
作者
Ruiz, Mario [1 ]
Wicker-Thomas, Claude [2 ,3 ]
Sanchez, Diego [1 ]
Ganfornina, Maria D. [1 ]
机构
[1] Univ Valladolid, CSIC, Inst Biol & Genet Mol, Dept Bioquim & Biol Mol & Fisiol, Valladolid 47003, Spain
[2] CNRS, UPR9034, LEGS, F-91198 Gif Sur Yvette, France
[3] Univ Paris Sud, F-91198 Gif Sur Yvette, France
关键词
Lipocalin; Oxidative stress; NLaz; Aging; Lipid storage; BILIN-BINDING PROTEIN; APOLIPOPROTEIN-D; MEMBRANE-RECEPTOR; DEVELOPMENTAL EXPRESSION; EMBRYONIC-DEVELOPMENT; DOPA-DECARBOXYLASE; LIFE-SPAN; GENE; BRAIN; INSECTICYANIN;
D O I
10.1016/j.ibmb.2012.07.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lazarillo (Laz) is a glycosyl-phosphatidylinositol (GPI)-linked glycoprotein first characterized in the developing nervous system of the grasshopper Schistocerca americana. It belongs to the Lipocalins, a functionally diverse family of mostly secreted proteins. In this work we test whether-the protective capacity known for Laz homologs in flies and vertebrates (NLaz, GLaz and ApoD) is evolutionarily conserved in grasshopper Laz, and can be exerted from the plasma membrane in a cell-autonomous manner. First we demonstrate that extracellular forms of Laz have autocrine and paracrine protecting effects for oxidative stress-challenged Drosophila S2 cells. Then we assay the effects of overexpressing GPI-linked Laz in adult Drosophila and whether it rescues both known and novel phenotypes of NLaz null mutants. Local effects of GPI-linked Laz inside and outside the nervous system promote survival upon different stress forms, and extend lifespan and healthspan of the flies in a cell-type dependent manner. Outside the nervous system, expression in fat body cells but not in hemocytes results in protection. Within the nervous system, glial cell expression is more effective than neuronal expression. Laz actions are sexually dimorphic in some expression domains. Fat storage promotion and not modifications in hydrocarbon profiles or quantities explain the starvation desiccation resistance caused by Laz overexpression. This effect is exerted when Laz is expressed ubiquitously or in dopaminergic cells, but not in hemocytes. Grasshopper Laz functionally restores the loss of NLaz, rescuing stress-sensitivity as well as premature accumulation of aging-related damage, monitored by advanced glycation end products (AGEs). However Laz does not rescue NLaz courtship behavioral defects. Finally, the presence of two new Lipocalins with predicted GPI-anchors in mosquitoes shows that the functional advantages of GPI-linkage have been commonly exploited by Lipocalins in the arthropodan lineage. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:776 / 789
页数:14
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