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Printable Handouts
Navigable Slide Index
- Introduction
- Malaria - risk areas
- Malaria infection in vertebrates
- Plasmodium intraerithrocytic cycle
- Molecular machinery of signal transduction
- ATP release upon RBC deformation
- Testing the effect of ATP on P. falciparum in RBCs
- P.f. invasion into RBC involves a purinoreceptor
- ATP induces Ca rise & affects P.f. invasion of RBC
- Studying the role of Ca in protease modulation
- Purinergic receptors in P. berghei and P. yoelii
- ATP induces cytosolic Ca increase
- KN-62 changes MSP1 processing
- Simultaneous Ca imaging in the PV and cytosol
- Role of high Ca concentration at the PV
- Ca measurements at PVM - comments on paper
- The striking synchronicity of P. falciparum cycle
- Synchronization & melatonin transduction pathway
- Ca and mitochondria
- Ca uptake by plasmodium mitochondria
- cAMP and Ca interplay in P. falciparum
- Tryptophan catabolism & P. falciparum cell cycle
- Melatonin doesn't affect asynchronous infections
- IP3 dependent Ca signaling
- IP3 liberation upon UV pulse
- IP3 induces Ca2+ rise in infected erythrocytes
- Melatonin affects inositol polyphosphate levels
- Downstream effectors on parasite synchronization
- PfPK7 KO cell cycle not affected by melatonin
- Ca rise in PfPK7 KO parasites was reduced
- Melatonin affects PfNEK2 & PfNEK3 KO cell cycle
- Molecular effectors of 2nd messengers signaling
- Transcription factors in Plasmodium
- PfNF-YB-expressed in P.f. intraerythrocytic stages
- cAMP induces differential expression of PfNF-YB
- G-protein coupled receptors
- Detecting GPCR-like receptors in P. falciparum
- P. falciparum GPCR transcripts at RBC cycle
- SR10 P. falciparum GPCR localization
- Conclusions
- Acknowledgments
- References
Topics Covered
- Plasmodium signaling
- Control of the cell cycle mechanisms
- Clinical and diagnostic applications in malarial research
- Live cell microscope work
- Molecular techniques
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Regina da Silva Garcia, C. (2012, October 31). Cellular signaling on host-malaria parasite interactions [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/BUDN4457.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Dr. Celia Regina da Silva Garcia has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Cell Biology
Transcript
Please wait while the transcript is being prepared...
0:00
Hello!
My name is Celia Garcia, I'm a
professor at the University of Sao
Paulo, Brazil, and
the title of my talk
is "Cellular Signaling
on Host-Malaria Parasite
Interactions."
0:14
Malaria is a devastating disease
and often lethal infection,
with a mortality of up to
a million people per year,
and is transmitted by a
parasite of genus Plasmodium.
0:26
In vertebrates, malaria
infection's initiated by the bite
of the Anopheles mosquito,
when she draws three to four
microliters of blood
while injecting saliva
containing a few sporozoites.
Once in the bloodstream, the
sporozoites invade the hepatocytes
and develop into asexual
merozoites within 10 to 12 days.
During this period, the
infection is asymptomatic.
0:53
The pathogenicity becomes apparent
after the parasite cycle, when
parasites enter blood stream and
develop inside the red blood cells
through a stage known as ring, to
a more mature form-- throphozoite
and the schizont-- up to the moment
of the rupture of the host cells,
when merozoites were free to
invade new red blood cells.
Some merozoites differentiate
into gametocytes the mosquito
infective form of the parasite.
Unlike mammalian cells, where
we have a more clear picture
of cellular signaling and the
molecular machinery involved,
we do not know the vast majority
of cellular molecular mechanisms
that control the parasites
outside in development.
Therefore, the focus of our work is
to investigate cellular signaling
of host Plasmodium interactions
during red blood cell stages.