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Alain Grodet

Researcher at French Institute of Health and Medical Research

Publications -  23
Citations -  1989

Alain Grodet is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Apoptosis & Mitochondrion. The author has an hindex of 20, co-authored 23 publications receiving 1872 citations. Previous affiliations of Alain Grodet include Paris Diderot University & University of Paris.

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Release of OPA1 during Apoptosis Participates in the Rapid and Complete Release of Cytochrome c and Subsequent Mitochondrial Fragmentation

TL;DR: It is demonstrated that cytochrome c release during apoptosis precedes mitochondrial fragmentation, and it is suggested that an initial mitochondrial leak of OPA1 leads to cristae structural alterations and exposure of previously sequestered protein pools, permitting continued release in a feed-forward manner to completion.
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Bax/Bak-dependent release of DDP/TIMM8a promotes Drp1-mediated mitochondrial fission and mitoptosis during programmed cell death.

TL;DR: Following Bax/Bak-mediated mitochondrial outer membrane permeabilization (MOMP), IMS proteins released comprise not only apoptogenic factors such as cytochrome c involved in caspase activation but also DDP/TIMM8a, which activates Drp1-mediated fission to promote mitochondrial fragmentation and subsequently elimination during PCD.
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On the evolution of programmed cell death: apoptosis of the unicellular eukaryote Leishmania major involves cysteine proteinase activation and mitochondrion permeabilization.

TL;DR: It is reported that staurosporine, that induces apoptosis in all mammalian nucleated cells, also induces in L. major a death process with several cytoplasmic and nuclear features of apoptosis, including cell shrinkage, phosphatidyl serine exposure, maintenance of plasma membrane integrity, mitochondrial transmembrane potential (ΔΨm) loss and cytochrome c release, nuclear chromatin condensation and fragmentation, and DNA degradation.
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Adverse Effects of Industrial Multiwalled Carbon Nanotubes on Human Pulmonary Cells

TL;DR: It is demonstrated that MWCNT produced for industrial purposes exert adverse effects without being internalized by human epithelial and mesothelial pulmonary cell lines.