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1.
Bioorg Med Chem Lett ; 29(16): 2208-2217, 2019 08 15.
Article in English | MEDLINE | ID: mdl-31272795

ABSTRACT

Targeting nuclear receptor RORγ is recognized to be beneficial in multiple autoimmune disorders. We disclosed new indole analogues as potent RORγ inverse agonists. RO-2 as one of the potent and orally bioavailable compounds was evaluated in various models of autoimmune disorder. It showed potent suppression of downstream markers of RORγt activity in murine and human primary cells, ex vivo PD assay and in multiple animal models of autoimmune diseases. The results indicate the potential of these indole analogues as orally bioavailable small molecule inverse agonists of RORγt, efficacious in various Th17 driven models of autoimmune disorders.


Subject(s)
Autoimmune Diseases/drug therapy , Indoles/chemistry , Nuclear Receptor Subfamily 1, Group F, Member 3/agonists , Animals , Humans , Mice , Models, Molecular , Structure-Activity Relationship
2.
Dev Biol ; 379(1): 76-91, 2013 Jul 01.
Article in English | MEDLINE | ID: mdl-23623898

ABSTRACT

The cuticular hairs and sensory bristles that decorate the adult Drosophila epidermis and the denticles found on the embryo have been used in studies on planar cell polarity and as models for the cytoskeletal mediated morphogenesis of cellular extensions. ZP domain proteins have recently been found to be important for the morphogenesis of both denticles and bristles. Here we show that the ZP domain protein Dusky-like is a key player in hair morphogenesis. As is the case in bristles, in hairs dyl mutants display a dramatic phenotype that is the consequence of a failure to maintain the integrity of the extension after outgrowth. Hairs lacking dyl function are split, thinned, multipled and often very short. dyl is required for normal chitin deposition in hairs, but chitin is not required for the normal accumulation of Dyl, hence dyl acts upstream of chitin. A lack of chitin however, does not mimic the dyl hair phenotype, thus Dyl must have other targets in hair morphogenesis. One of these appears to be the actin cytoskeleton. Interestingly, dyl mutants also display a unique planar cell polarity phenotype that is distinct from that seen with mutations in the frizzled/starry night or dachsous/fat pathway genes. Rab11 was previously found to be essential for Dyl plasma membrane localization in bristles. Here we found that the expression of a dominant negative Rab11 can mimic the dyl hair morphology phenotype consistent with Rab11 also being required for Dyl function in hairs. We carried out a small directed screen to identify genes that might function with dyl and identified Chitinase 6 (Cht6) as a strong candidate, as knocking down Cht6 function led to weak versions of all of the dyl hair phenotypes.


Subject(s)
Cell Polarity , Drosophila Proteins/metabolism , Drosophila/growth & development , Gene Expression Regulation, Developmental , Hair/growth & development , Membrane Proteins/metabolism , Wings, Animal/growth & development , Animals , Chitin/metabolism , Chitinases/genetics , Chitinases/metabolism , Crosses, Genetic , Drosophila/anatomy & histology , Drosophila/genetics , Drosophila/metabolism , Drosophila Proteins/genetics , Female , Genes, Insect , Hair/metabolism , Hair/ultrastructure , Male , Membrane Proteins/genetics , Microscopy, Electron, Scanning , Morphogenesis , Mutation , Phenotype , Wings, Animal/anatomy & histology , Wings, Animal/metabolism , rab GTP-Binding Proteins/genetics , rab GTP-Binding Proteins/metabolism
3.
Development ; 139(5): 906-16, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22278919

ABSTRACT

The morphogenesis of Drosophila sensory bristles is dependent on the function of their actin and microtubule cytoskeleton. Actin filaments are important for bristle shape and elongation, while microtubules are thought to mediate protein and membrane trafficking to promote growth. We have identified an essential role for the bristle cuticle in the maintenance of bristle structure and shape at late stages of bristle development. We show that the small GTPase Rab11 mediates the organized deposition of chitin, a major cuticle component in bristles, and disrupting Rab11 function leads to phenotypes that result from bristle collapse rather than a failure to elongate. We further establish that Rab11 is required for the plasma membrane localization of the ZP domain-containing Dusky-like (Dyl) protein and that Dyl is also required for cuticle formation in bristles. Our data argue that Dyl functions as a Rab11 effector for mediating the attachment of the bristle cell membrane to chitin to establish a stable cuticle. Our studies also implicate the exocyst as a Rab11 effector in this process and that Rab11 trafficking along the bristle shaft is mediated by microtubules.


Subject(s)
Drosophila Proteins/metabolism , Drosophila melanogaster/growth & development , Drosophila melanogaster/ultrastructure , Membrane Proteins/metabolism , rab GTP-Binding Proteins/metabolism , Animals , Chitin/metabolism , Chitin Synthase/antagonists & inhibitors , Chitin Synthase/metabolism , Cytoplasm/metabolism , Cytoplasm/ultrastructure , Drosophila Proteins/genetics , Drosophila melanogaster/genetics , Membrane Proteins/genetics , Microtubules/metabolism , Microtubules/ultrastructure , Morphogenesis , Phenotype , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Transgenes , rab GTP-Binding Proteins/genetics
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