Stéphane Egée
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Stéphane Egée has a total of 35 co-authors. Here are the top co-authors by number of shared publications:
- Abdelrazak Aissat
Département de Biochimie‐Biologie Moléculaire, Pharmacologie, Génétique Médicale, AP‐HP Hôpitaux Universitaires Henri Mondor 51 Avenue du Maréchal de Lattre de Tassigny Créteil Val‐deMarne France
1 shared publication - Abdoulaye Sissoko
INSERM-U1134, BIGR, Universite Paris Cite and Universite des Antilles, Paris, France
1 shared publication - Anthony Marteau
Parasitology-Mycology Department, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, 93009 Bobigny, France
1 shared publication - Ariane Lunati‐Rozie
Département de Biochimie‐Biologie Moléculaire, Pharmacologie, Génétique Médicale, AP‐HP Hôpitaux Universitaires Henri Mondor Créteil France
1 shared publication - Benoît Funalot
Département de Biochimie‐Biologie Moléculaire, Pharmacologie, Génétique Médicale, AP‐HP Hôpitaux Universitaires Henri Mondor 51 Avenue du Maréchal de Lattre de Tassigny Créteil Val‐deMarne France
1 shared publication - Bertrand Godeau
Department of Internal Medicine and Clinical Immunology, coordinating center of the national reference center for adult' immune cytopenias, Henri Mondor university hospital, Assistance Publique Hôpitaux de Paris, Université Paris-Est Créteil, Paris, France
1 shared publication
Latest Publications
- Open Access
- 18 May 2021
- Published by Wiley in American Journal of Hematology
- Vol. 96 (9) , E318-E321
Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation
- 18 May 2021
- Published by Wiley in American Journal of Hematology
- Vol. 96 (9) , E318-E321
Open AccessMultiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation
- Open Access
Plasmodium falciparum sexual parasites regulate infected erythrocyte permeability
To ensure the transport of nutrients necessary for their survival, Plasmodium falciparum parasites increase erythrocyte permeability to diverse solutes. These New Permeation Pathways (NPP) have been extensively characterized in the pathogenic asexual parasite stages, however the existence of NPP has never been investigated in gametocytes, the sexual stages responsible for transmission to mosquitoes. Here, we show that NPP are still active in erythrocytes infected with immature gametocytes and that this activity declines along gametocyte maturation. Our results indicate that NPP are regulated by cyclic AMP (cAMP) signaling cascade during sexual parasite stages, and that the decrease in cAMP levels in mature stages results in a slowdown of NPP activity. We also show that NPP facilitate the uptake of artemisinin derivatives and that phosphodiesterase (PDE) inhibitors can reactivate NPP and increase drug uptake in mature gametocyte-infected erythrocytes. These processes are predicted to play a key role in P. falciparum gametocyte biology and susceptibility to antimalarials.
Open AccessPlasmodium falciparum sexual parasites regulate infected erythrocyte permeability
To ensure the transport of nutrients necessary for their survival, Plasmodium falciparum parasites increase erythrocyte permeability to diverse solutes. These New Permeation Pathways (NPP) have been extensively characterized in the pathogenic asexual parasite stages, however the existence of NPP has never been investigated in gametocytes, the sexual stages responsible for transmission to mosquitoes. Here, we show that NPP are still active in erythrocytes infected with immature gametocytes and that this activity declines along gametocyte maturation. Our results indicate that NPP are regulated by cyclic AMP (cAMP) signaling cascade during sexual parasite stages, and that the decrease in cAMP levels in mature stages results in a slowdown of NPP activity. We also show that NPP facilitate the uptake of artemisinin derivatives and that phosphodiesterase (PDE) inhibitors can reactivate NPP and increase drug uptake in mature gametocyte-infected erythrocytes. These processes are predicted to play a key role in P. falciparum gametocyte biology and susceptibility to antimalarials.