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Undead cells up-regulate cytosolic Ca2+ signaling and produce Ca2+ flashes in a Dronc-dependent manner. Top: The disc outline is marked by yellow dashed lines. The white dotted lines highlight the ey-Gal4-expressing area of the eye discs. For all panels, scale bars are 50 μm. Confocal images of third instar larval eye imaginal disc expressing the Ca2+ reporter GCaMP6s in control (ey-Gal4, left, and ey>p35, middle) and in overgrown, undead (ey>hid,p35, right) discs. The GCaMP6s fluorescence directly represents the cytosolic Ca2+ level. The cytosolic Ca2+ level is significantly upregulated in undead (ey>hid,p35) discs compared to control discs (see white arrows in righthand panel). Bottom: Representative Ca2+ traces of eye imaginal discs expressing GCaMP6s obtained by time-lapse confocal imaging (600 frames, 1-second intervals). Ca²⁺ flashes refer to transient, localized increases in intracellular calcium levels, detected as brief bursts of elevated GCaMP6s fluorescence. These flashes are characterized by a rapid onset, short duration, and return to baseline, indicating discrete calcium signaling events within imaginal disc cells. Each line represents an independent disc (numbered). Undead discs display a strong increase in the number of Ca2+ flashes. Genotypes as for top row.

Undead cells up-regulate cytosolic Ca2+ signaling and produce Ca2+ flashes in a Dronc-dependent manner. Top: The disc outline is marked by yellow dashed lines. The white dotted lines highlight the ey-Gal4-expressing area of the eye discs. For all panels, scale bars are 50 μm. Confocal images of third instar larval eye imaginal disc expressing the Ca2+ reporter GCaMP6s in control (ey-Gal4, left, and ey>p35, middle) and in overgrown, undead (ey>hid,p35, right) discs. The GCaMP6s fluorescence directly represents the cytosolic Ca2+ level. The cytosolic Ca2+ level is significantly upregulated in undead (ey>hid,p35) discs compared to control discs (see white arrows in righthand panel). Bottom: Representative Ca2+ traces of eye imaginal discs expressing GCaMP6s obtained by time-lapse confocal imaging (600 frames, 1-second intervals). Ca²⁺ flashes refer to transient, localized increases in intracellular calcium levels, detected as brief bursts of elevated GCaMP6s fluorescence. These flashes are characterized by a rapid onset, short duration, and return to baseline, indicating discrete calcium signaling events within imaginal disc cells. Each line represents an independent disc (numbered). Undead discs display a strong increase in the number of Ca2+ flashes. Genotypes as for top row.

The initiator #caspase Dronc can trigger compensatory #apoptosis -induced proliferation (AiP). This study shows that Dronc-dependent Ca2+ influx into the cytosol is an important contributor to AiP & DUOX activation in #Drosophila (& likely in vertebrates) @plosbiology.org 🧪 plos.io/4pNG4PK

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Undead cells up-regulate cytosolic Ca2+ signaling and produce Ca2+ flashes in a Dronc-dependent manner. Top: The disc outline is marked by yellow dashed lines. The white dotted lines highlight the ey-Gal4-expressing area of the eye discs. For all panels, scale bars are 50 μm. Confocal images of third instar larval eye imaginal disc expressing the Ca2+ reporter GCaMP6s in control (ey-Gal4, left, and ey>p35, middle) and in overgrown, undead (ey>hid,p35, right) discs. The GCaMP6s fluorescence directly represents the cytosolic Ca2+ level. The cytosolic Ca2+ level is significantly upregulated in undead (ey>hid,p35) discs compared to control discs (see white arrows in righthand panel). Bottom: Representative Ca2+ traces of eye imaginal discs expressing GCaMP6s obtained by time-lapse confocal imaging (600 frames, 1-second intervals). Ca²⁺ flashes refer to transient, localized increases in intracellular calcium levels, detected as brief bursts of elevated GCaMP6s fluorescence. These flashes are characterized by a rapid onset, short duration, and return to baseline, indicating discrete calcium signaling events within imaginal disc cells. Each line represents an independent disc (numbered). Undead discs display a strong increase in the number of Ca2+ flashes. Genotypes as for top row.

Undead cells up-regulate cytosolic Ca2+ signaling and produce Ca2+ flashes in a Dronc-dependent manner. Top: The disc outline is marked by yellow dashed lines. The white dotted lines highlight the ey-Gal4-expressing area of the eye discs. For all panels, scale bars are 50 μm. Confocal images of third instar larval eye imaginal disc expressing the Ca2+ reporter GCaMP6s in control (ey-Gal4, left, and ey>p35, middle) and in overgrown, undead (ey>hid,p35, right) discs. The GCaMP6s fluorescence directly represents the cytosolic Ca2+ level. The cytosolic Ca2+ level is significantly upregulated in undead (ey>hid,p35) discs compared to control discs (see white arrows in righthand panel). Bottom: Representative Ca2+ traces of eye imaginal discs expressing GCaMP6s obtained by time-lapse confocal imaging (600 frames, 1-second intervals). Ca²⁺ flashes refer to transient, localized increases in intracellular calcium levels, detected as brief bursts of elevated GCaMP6s fluorescence. These flashes are characterized by a rapid onset, short duration, and return to baseline, indicating discrete calcium signaling events within imaginal disc cells. Each line represents an independent disc (numbered). Undead discs display a strong increase in the number of Ca2+ flashes. Genotypes as for top row.

The initiator #caspase Dronc can trigger compensatory #apoptosis -induced proliferation (AiP). This study shows that Dronc-dependent Ca2+ influx into the cytosol is an important contributor to AiP & DUOX activation in #Drosophila (& likely in vertebrates) @plosbiology.org 🧪 plos.io/4pNG4PK

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Undead cells up-regulate cytosolic Ca2+ signaling and produce Ca2+ flashes in a Dronc-dependent manner. Top: The disc outline is marked by yellow dashed lines. The white dotted lines highlight the ey-Gal4-expressing area of the eye discs. For all panels, scale bars are 50 μm. Confocal images of third instar larval eye imaginal disc expressing the Ca2+ reporter GCaMP6s in control (ey-Gal4, left, and ey>p35, middle) and in overgrown, undead (ey>hid,p35, right) discs. The GCaMP6s fluorescence directly represents the cytosolic Ca2+ level. The cytosolic Ca2+ level is significantly upregulated in undead (ey>hid,p35) discs compared to control discs (see white arrows in righthand panel). Bottom: Representative Ca2+ traces of eye imaginal discs expressing GCaMP6s obtained by time-lapse confocal imaging (600 frames, 1-second intervals). Ca²⁺ flashes refer to transient, localized increases in intracellular calcium levels, detected as brief bursts of elevated GCaMP6s fluorescence. These flashes are characterized by a rapid onset, short duration, and return to baseline, indicating discrete calcium signaling events within imaginal disc cells. Each line represents an independent disc (numbered). Undead discs display a strong increase in the number of Ca2+ flashes. Genotypes as for top row.

Undead cells up-regulate cytosolic Ca2+ signaling and produce Ca2+ flashes in a Dronc-dependent manner. Top: The disc outline is marked by yellow dashed lines. The white dotted lines highlight the ey-Gal4-expressing area of the eye discs. For all panels, scale bars are 50 μm. Confocal images of third instar larval eye imaginal disc expressing the Ca2+ reporter GCaMP6s in control (ey-Gal4, left, and ey>p35, middle) and in overgrown, undead (ey>hid,p35, right) discs. The GCaMP6s fluorescence directly represents the cytosolic Ca2+ level. The cytosolic Ca2+ level is significantly upregulated in undead (ey>hid,p35) discs compared to control discs (see white arrows in righthand panel). Bottom: Representative Ca2+ traces of eye imaginal discs expressing GCaMP6s obtained by time-lapse confocal imaging (600 frames, 1-second intervals). Ca²⁺ flashes refer to transient, localized increases in intracellular calcium levels, detected as brief bursts of elevated GCaMP6s fluorescence. These flashes are characterized by a rapid onset, short duration, and return to baseline, indicating discrete calcium signaling events within imaginal disc cells. Each line represents an independent disc (numbered). Undead discs display a strong increase in the number of Ca2+ flashes. Genotypes as for top row.

The initiator #caspase Dronc can trigger compensatory #apoptosis -induced proliferation (AiP). This study shows that Dronc-dependent Ca2+ influx into the cytosol is an important contributor to AiP & DUOX activation in #Drosophila (& likely in vertebrates) @plosbiology.org 🧪 plos.io/4pNG4PK

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bsky.app/profile/did:...

#DOPAMINA
multi-search-tag-explorer.allgraph.ro/advanced-sea...
#CASPASE
multi-search-tag-explorer.allgraph.ro/advanced-sea...
allgraph.ro

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Left: representative images of livers with staining of the hepatocyte marker HNF4α, cholangiocyte marker CK19, the Kupffer cell marker CD68 or the endothelial cell marker CD31. Right: Schematic showing the regulation of JAK/STAT3 pathway by executioner caspases.

Left: representative images of livers with staining of the hepatocyte marker HNF4α, cholangiocyte marker CK19, the Kupffer cell marker CD68 or the endothelial cell marker CD31. Right: Schematic showing the regulation of JAK/STAT3 pathway by executioner caspases.

Some executioner caspases also have non-apoptotic functions. This study shows that sublethal executioner #caspase activation enhances #hepatocyte proliferation via JAK/STAT3 signaling, revealing a role for executioner caspases in promoting liver #regeneration @plosbiology.org 🧪 plos.io/3JEsH57

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Left: representative images of livers with staining of the hepatocyte marker HNF4α, cholangiocyte marker CK19, the Kupffer cell marker CD68 or the endothelial cell marker CD31. Right: Schematic showing the regulation of JAK/STAT3 pathway by executioner caspases.

Left: representative images of livers with staining of the hepatocyte marker HNF4α, cholangiocyte marker CK19, the Kupffer cell marker CD68 or the endothelial cell marker CD31. Right: Schematic showing the regulation of JAK/STAT3 pathway by executioner caspases.

Some executioner caspases also have non-apoptotic functions. This study shows that sublethal executioner #caspase activation enhances #hepatocyte proliferation via JAK/STAT3 signaling, revealing a role for executioner caspases in promoting liver #regeneration @plosbiology.org 🧪 plos.io/3JEsH57

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Left: representative images of livers with staining of the hepatocyte marker HNF4α, cholangiocyte marker CK19, the Kupffer cell marker CD68 or the endothelial cell marker CD31. Right: Schematic showing the regulation of JAK/STAT3 pathway by executioner caspases.

Left: representative images of livers with staining of the hepatocyte marker HNF4α, cholangiocyte marker CK19, the Kupffer cell marker CD68 or the endothelial cell marker CD31. Right: Schematic showing the regulation of JAK/STAT3 pathway by executioner caspases.

Some executioner caspases also have non-apoptotic functions. This study shows that sublethal executioner #caspase activation enhances #hepatocyte proliferation via JAK/STAT3 signaling, revealing a role for executioner caspases in promoting liver #regeneration @plosbiology.org 🧪 plos.io/3JEsH57

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DNA damage caused by #ChromosomalInstability boosts #cancer cell invasiveness. #Caspase activation plays a key role in this process.

Image by Mariana Muzzopappa, from @milanlab.bsky.social.

📌 https://doi.org/10.1016/j.cub.2023.09.004

🧪🐡

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Preview
Inflammasome signaling in astrocytes modulates hippocampal plasticity The function of immune pathways in homeostatic neurobiology remains underexplored. Zengeler et al. find that the inflammasome complex, typically associated with immune responses, is involved in memory...

Los inflamasomas son complejos multiproteicos que promueven la producción de interleucina (IL)-1 e IL-18 en respuesta a patógenos y daño tisular. Se autoregula en astrocitos del Hipocampo en respuesta al aprendizaje y la actividad.
#Astrocitos #Neurología #Caspase
www.cell.com/immunity/ful...

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Published on February 28, 2024, in Genes & Diseases, researchers have identified Ferroptosis Suppressor Protein 1 (FSP1) as a central factor in intervertebral disc degeneration.
#Caspase 3 #FSP1
Details: doi.org/10.1016/j.gendis.2024.101251

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Rupert Beale @bealelab.bsky.social and co-workers @crick.ac.uk @imperialcollegeldn.bsky.social show that #caspase cleavage of #influenza A #virus M2 disrupts M2-LC3 interaction and regulates virion production.

-> www.embopress.org/doi/full/10....

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Top: Graphical representation of current working model. Bottom: Representative immunofluorescence images of SKBR3 parental, DKO or CASP3 + 7-WT re-expression in DKO cells treated with 0.25 µM DALGreen in fed (top row) or starved (bottom row) conditions. BafA1 in both fed and starved conditions serves as controls.

Top: Graphical representation of current working model. Bottom: Representative immunofluorescence images of SKBR3 parental, DKO or CASP3 + 7-WT re-expression in DKO cells treated with 0.25 µM DALGreen in fed (top row) or starved (bottom row) conditions. BafA1 in both fed and starved conditions serves as controls.

Caspases have well known roles in #apoptosis, but roles in other cellular processes are emerging... This study shows that #caspase -3 & -7 promote cytoprotective #autophagy in response to non-lethal stress by modulating PARP1 activity in #BreastCancer cells 🧪 @plosbiology.org plos.io/41xfLVm

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Top: Graphical representation of current working model. Bottom: Representative immunofluorescence images of SKBR3 parental, DKO or CASP3 + 7-WT re-expression in DKO cells treated with 0.25 µM DALGreen in fed (top row) or starved (bottom row) conditions. BafA1 in both fed and starved conditions serves as controls.

Top: Graphical representation of current working model. Bottom: Representative immunofluorescence images of SKBR3 parental, DKO or CASP3 + 7-WT re-expression in DKO cells treated with 0.25 µM DALGreen in fed (top row) or starved (bottom row) conditions. BafA1 in both fed and starved conditions serves as controls.

Caspases have well known roles in #apoptosis, but roles in other cellular processes are emerging... This study shows that #caspase -3 & -7 promote cytoprotective #autophagy in response to non-lethal stress by modulating PARP1 activity in #BreastCancer cells 🧪 @plosbiology.org plos.io/41xfLVm

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Top: Graphical representation of current working model. Bottom: Representative immunofluorescence images of SKBR3 parental, DKO or CASP3 + 7-WT re-expression in DKO cells treated with 0.25 µM DALGreen in fed (top row) or starved (bottom row) conditions. BafA1 in both fed and starved conditions serves as controls.

Top: Graphical representation of current working model. Bottom: Representative immunofluorescence images of SKBR3 parental, DKO or CASP3 + 7-WT re-expression in DKO cells treated with 0.25 µM DALGreen in fed (top row) or starved (bottom row) conditions. BafA1 in both fed and starved conditions serves as controls.

Caspases have well known roles in #apoptosis, but roles in other cellular processes are emerging... This study shows that #caspase -3 & -7 promote cytoprotective #autophagy in response to non-lethal stress by modulating PARP1 activity in #BreastCancer cells 🧪 @plosbiology.org plos.io/41xfLVm

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#CotM: at the start of the year we look at the end of a cell's life: the #caspase cascade activates #apoptosis:
e.g. Casp-6 autocleaves or is cleaved by Casp-3,-8,-10 & cleaves Casp-2,-8,-10 and affects the apoptosome (incl. Casp-9):@PDBeurope #3p45

ebi.ac.uk/complexportal/…

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