Induction of proinflammatory responses in macrophages by the glycosylphosphatidylinositols of Plasmodium falciparum: cell signaling receptors, glycosylphosphatidylinositol (GPI) structural requirement, and regulation of GPI activity (Q28579420)

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English	Induction of proinflammatory responses in macrophages by the glycosylphosphatidylinositols of Plasmodium falciparum: cell signaling receptors, glycosylphosphatidylinositol (GPI) structural requirement, and regulation of GPI activity	scientific journal article

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scholarly article

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PubMed publication ID

31 January 2017

Induction of proinflammatory responses in macrophages by the glycosylphosphatidylinositols of Plasmodium falciparum: cell signaling receptors, glycosylphosphatidylinositol (GPI) structural requirement, and regulation of GPI activity (English)

1 reference

PubMed publication ID

31 January 2017

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Plasmodium falciparum

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6

object named as

Shizuo Akira

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7

object named as

Amina S. Woods

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PubMed publication ID

31 January 2017

author name string

Gowdahalli Krishnegowda

1

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PubMed publication ID

31 January 2017

Adeline M. Hajjar

2

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PubMed publication ID

31 January 2017

Jianzhong Zhu

3

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PubMed publication ID

31 January 2017

Erika J. Douglass

4

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PubMed publication ID

31 January 2017

Satoshi Uematsu

5

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PubMed publication ID

31 January 2017

D. Channe Gowda

8

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PubMed publication ID

31 January 2017

language of work or name

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publication date

4 March 2005

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PubMed publication ID

31 January 2017

Journal of Biological Chemistry

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PubMed publication ID

31 January 2017

280

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PubMed publication ID

31 January 2017

9

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PubMed publication ID

31 January 2017

8606–8616

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PubMed publication ID

31 January 2017

Toll-like receptors 9 and 3 as essential components of innate immune defense against mouse cytomegalovirus infection

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Toll-like receptors

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A phospholipase D specific for the phosphatidylinositol anchor of cell-surface proteins is abundant in plasma

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Synchronization of Plasmodium falciparum Erythrocytic Stages in Culture

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Host age as a determinant of naturally acquired immunity to Plasmodium falciparum

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Malarial toxins and the regulation of parasite density

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Transfer of exogenous glycosylphos-phatidylinositol (GPI)-linked molecules to plasma membranes

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Structure and activity of glycosylphosphatidylinositol anchors of Plasmodium falciparum

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Proinflammatory activity of glycosylphosphatidylinositol anchors derived from Trypanosoma cruzi: structural and functional analyses.

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Activation of Toll-like receptor-2 by glycosylphosphatidylinositol anchors from a protozoan parasite

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Plasmodium falciparum glycosylphosphatidylinositol-induced TNF-alpha secretion by macrophages is mediated without membrane insertion or endocytosis

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29 September 2017

Glycosylphosphatidylinositol anchors of Plasmodium falciparum: molecular characterization and naturally elicited antibody response that may provide immunity to malaria pathogenesis

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Signaling of immune system cells by glycosylphosphatidylinositol (GPI) anchor and related structures derived from parasitic protozoa.

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Central role of endogenous gamma interferon in protective immunity against blood-stage Plasmodium chabaudi AS infection

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Highly purified glycosylphosphatidylinositols from Trypanosoma cruzi are potent proinflammatory agents

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Premunition in Plasmodium falciparum infection: insights from the epidemiology of multiple infections.

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Glycosylphosphatidylinositol-specific phospholipase D is expressed by macrophages in human atherosclerosis and colocalizes with oxidation epitopes

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Signal transduction in macrophages by glycosylphosphatidylinositols of Plasmodium, Trypanosoma, and Leishmania: activation of protein tyrosine kinases and protein kinase C by inositolglycan and diacylglycerol moieties

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Secretory phospholipases A2.

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Signal transduction in host cells by a glycosylphosphatidylinositol toxin of malaria parasites

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The structure and biosynthesis of glycosyl phosphatidylinositol protein anchors

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Neutralizing monoclonal antibodies to glycosylphosphatidylinositol, the dominant TNF-alpha-inducing toxin of Plasmodium falciparum: prospects for the immunotherapy of severe malaria.

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