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The Trypanosoma brucei TbHrg protein is a heme transporter involved in the regulation of stage-specific morphological transitions
E. Horáková, P. Changmai, M. Vancová, R. Sobotka, J. Van Den Abbeele, B. Vanhollebeke, J. Lukeš,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 2008 do Před 1 rokem
Freely Accessible Science Journals
od 1905 do Před 1 rokem
PubMed Central
od 2005
Europe PubMed Central
od 2005 do Před 1 rokem
Open Access Digital Library
od 1905-10-01
Open Access Digital Library
od 1905-10-01
ROAD: Directory of Open Access Scholarly Resources
od 1905
PubMed
28232490
DOI
10.1074/jbc.m116.762997
Knihovny.cz E-zdroje
- MeSH
- biologický transport MeSH
- down regulace MeSH
- flagella metabolismus MeSH
- hem metabolismus MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- membránové transportní proteiny metabolismus MeSH
- mikroskopie elektronová rastrovací MeSH
- moucha tse-tse parazitologie MeSH
- proliferace buněk MeSH
- protozoální proteiny metabolismus MeSH
- receptory buněčného povrchu metabolismus MeSH
- RNA interference MeSH
- sekvence aminokyselin MeSH
- stadia vývoje MeSH
- transgeny MeSH
- Trypanosoma brucei brucei metabolismus MeSH
- vývojová regulace genové exprese MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
The human parasite Trypanosoma brucei does not synthesize heme de novo and instead relies entirely on heme supplied by its vertebrate host or its insect vector, the tsetse fly. In the host bloodstream T. brucei scavenges heme via haptoglobin-hemoglobin (HpHb) receptor-mediated endocytosis occurring in the flagellar pocket. However, in the procyclic developmental stage, in which T. brucei is confined to the tsetse fly midgut, this receptor is apparently not expressed, suggesting that T. brucei takes up heme by a different, unknown route. To define this alternative route, we functionally characterized heme transporter TbHrg in the procyclic stage. RNAi-induced down-regulation of TbHrg in heme-limited culture conditions resulted in slower proliferation, decreased cellular heme, and marked changes in cellular morphology so that the cells resemble mesocyclic trypomastigotes. Nevertheless, the TbHrg KO developed normally in the tsetse flies at rates comparable with wild-type cells. T. brucei cells overexpressing TbHrg displayed up-regulation of the early procyclin GPEET and down-regulation of the late procyclin EP1, two proteins coating the T. brucei surface in the procyclic stage. Light microscopy of immunostained TbHrg indicated localization to the flagellar membrane, and scanning electron microscopy revealed more intense TbHrg accumulation toward the flagellar pocket. Based on these findings, we postulate that T. brucei senses heme levels via the flagellar TbHrg protein. Heme deprivation in the tsetse fly anterior midgut might represent an environmental stimulus involved in the transformation of this important human parasite, possibly through metabolic remodeling.
Citace poskytuje Crossref.org
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- $a Horáková, Eva $u From the Institute of Parasitology, Biology Center, Czech Academy of Sciences, 37005 České Budějovice (Budweis), Czech Republic.
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- $a The human parasite Trypanosoma brucei does not synthesize heme de novo and instead relies entirely on heme supplied by its vertebrate host or its insect vector, the tsetse fly. In the host bloodstream T. brucei scavenges heme via haptoglobin-hemoglobin (HpHb) receptor-mediated endocytosis occurring in the flagellar pocket. However, in the procyclic developmental stage, in which T. brucei is confined to the tsetse fly midgut, this receptor is apparently not expressed, suggesting that T. brucei takes up heme by a different, unknown route. To define this alternative route, we functionally characterized heme transporter TbHrg in the procyclic stage. RNAi-induced down-regulation of TbHrg in heme-limited culture conditions resulted in slower proliferation, decreased cellular heme, and marked changes in cellular morphology so that the cells resemble mesocyclic trypomastigotes. Nevertheless, the TbHrg KO developed normally in the tsetse flies at rates comparable with wild-type cells. T. brucei cells overexpressing TbHrg displayed up-regulation of the early procyclin GPEET and down-regulation of the late procyclin EP1, two proteins coating the T. brucei surface in the procyclic stage. Light microscopy of immunostained TbHrg indicated localization to the flagellar membrane, and scanning electron microscopy revealed more intense TbHrg accumulation toward the flagellar pocket. Based on these findings, we postulate that T. brucei senses heme levels via the flagellar TbHrg protein. Heme deprivation in the tsetse fly anterior midgut might represent an environmental stimulus involved in the transformation of this important human parasite, possibly through metabolic remodeling.
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- $a Changmai, Piya $u From the Institute of Parasitology, Biology Center, Czech Academy of Sciences, 37005 České Budějovice (Budweis), Czech Republic.
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- $a Vancová, Marie $u From the Institute of Parasitology, Biology Center, Czech Academy of Sciences, 37005 České Budějovice (Budweis), Czech Republic. Faculty of Sciences, University of South Bohemia, 37005 České Budějovice (Budweis), Czech Republic.
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- $a Sobotka, Roman $u Faculty of Sciences, University of South Bohemia, 37005 České Budějovice (Budweis), Czech Republic. Institute of Microbiology, Czech Academy of Sciences, 37981 Třeboň, Czech Republic.
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- $a Lukeš, Julius $u From the Institute of Parasitology, Biology Center, Czech Academy of Sciences, 37005 České Budějovice (Budweis), Czech Republic, jula@paru.cas.cz. Faculty of Sciences, University of South Bohemia, 37005 České Budějovice (Budweis), Czech Republic. Canadian Institute for Advanced Research, Toronto, Ontario M5G 1Z8, Canada.
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