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2.
Phytochemistry ; 184: 112669, 2021 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-33524856

RESUMO

Neem (Azadirachta indica L.) is well known for its medicinal, agricultural, and pesticidal applications since ages. The secondary metabolites, limonoids, confer these biological properties, wherein over 150 different limonoids have been reported from neem. To understand limonoid biosynthesis, we analyzed tissue-specific (kernel, pericarp, leaves, and flower) transcriptome that resulted in the identification of one farnesyl diphosphate synthase (AiFDS), one squalene synthase (AiSQS), three squalene epoxidases (AiSQE1, AiSQE2, and AiSQE3), two triterpene synthases (AiTTS1 and AiTTS2), cycloartenol synthase (AiCAS), two cytochrome P450 reductases, and ten cytochrome P450 systems. Comparative tissue-expression analysis indicated that AiFDS, AiSQS, AiSQE3, and AiTTS1 are expressed higher in the kernel than in the other tissues. Heterologously expressed recombinant AiTTS1 produced tirucalla-7,24-dien-3ß-ol as the sole product. Expression profile data, phylogeny with triterpene synthases from Meliaceae and Rutaceae families, real-time PCR of different tissues, and transient transformation revealed the involvement of tirucalla-7,24-dien-3ß-ol synthase (AiTTS1) in limonoid biosynthesis. Further, mutagenesis studies of AiTTS1 indicated that Y125 and F260 are probably involved in stabilization of dammarenyl cation. A 2.6-fold increase in production of tirucalla-7,24-dien-3ß-ol was observed when AiSQE1 was co-expressed with mutant AiTTS1 in a yeast system. Furthermore, we functionally characterized the highly expressed cytochrome P450 reductases and cycloartenol synthase. This study helps in further analysis and identification of genes involved in limonoid biosynthesis in Meliaceae/Rutaceae and their production in a metabolically tractable heterologous system.


Assuntos
Azadirachta , Limoninas , Meliaceae , Triterpenos , Folhas de Planta/genética
3.
Mucosal Immunol ; 9(5): 1250-62, 2016 09.
Artigo em Inglês | MEDLINE | ID: mdl-26838049

RESUMO

Inflammatory bowel disease (IBD) is associated with dysregulated macrophage responses, such that quiescent macrophages acquire a pro-inflammatory activation state and contribute to chronic intestinal inflammation. The transcriptional events governing macrophage activation and gene expression in the context of chronic inflammation such as IBD remain incompletely understood. Here, we identify Kruppel-like transcription factor-6 (KLF6) as a critical regulator of pathogenic myeloid cell activation in human and experimental IBD. We found that KLF6 was significantly upregulated in myeloid cells and intestinal tissue from IBD patients and experimental models of IBD, particularly in actively inflamed regions of the colon. Using complementary gain- and loss-of-function studies, we observed that KLF6 promotes pro-inflammatory gene expression through enhancement of nuclear factor κB (NFκB) signaling, while simultaneously suppressing anti-inflammatory gene expression through repression of signal transducer and activator of transcription 3 (STAT3) signaling. To study the in vivo role of myeloid KLF6, we treated myeloid-specific KLF6-knockout mice (Mac-KLF6-KO) with dextran sulfate sodium (DSS) and found that Mac-KLF6-KO mice were protected against chemically-induced colitis; this highlights the central role of myeloid KLF6 in promoting intestinal inflammation. Collectively, our results point to a novel gene regulatory program underlying pathogenic, pro-inflammatory macrophage activation in the setting of chronic intestinal inflammation.


Assuntos
Colite Ulcerativa/imunologia , Colite/imunologia , Colo/imunologia , Doença de Crohn/imunologia , Fatores de Transcrição Kruppel-Like/imunologia , Macrófagos/imunologia , Proteínas Proto-Oncogênicas/imunologia , Animais , Linhagem Celular , Plasticidade Celular/imunologia , Colite/induzido quimicamente , Colite/genética , Colite/patologia , Colite Ulcerativa/genética , Colite Ulcerativa/patologia , Colo/patologia , Doença de Crohn/genética , Doença de Crohn/patologia , Sulfato de Dextrana , Regulação da Expressão Gênica , Humanos , Fator 6 Semelhante a Kruppel , Fatores de Transcrição Kruppel-Like/deficiência , Fatores de Transcrição Kruppel-Like/genética , Ativação de Macrófagos , Macrófagos/patologia , Masculino , Camundongos , Camundongos Knockout , Monócitos/imunologia , Monócitos/patologia , NF-kappa B/genética , NF-kappa B/imunologia , Proteínas Proto-Oncogênicas/deficiência , Proteínas Proto-Oncogênicas/genética , Fator de Transcrição STAT3/genética , Fator de Transcrição STAT3/imunologia , Transdução de Sinais , Transcrição Gênica
4.
Phys Rev Lett ; 95(17): 175003, 2005 Oct 21.
Artigo em Inglês | MEDLINE | ID: mdl-16383835

RESUMO

Three kinds of electrostatic modes are experimentally observed to propagate along magnetic-field lines for the first time in the pair-ion plasma consisting of only positive and negative fullerene ions with an equal mass. It is found that the phase lag between the density fluctuations of positive and negative ions varies from 0 to pi depending on the frequency for ion acoustic wave and is fixed at pi for an ion plasma wave. In addition, a new mode with the phase lag about pi appears in an intermediate-frequency band between the frequency ranges of the acoustic and plasma waves.

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