Presentation is loading. Please wait.

Presentation is loading. Please wait.

Mitochondria localize to both the front and the rear of neutrophils.

Published byθάλασσα Ανδρέου Modified over 6 years ago

Similar presentations

Presentation on theme: "Mitochondria localize to both the front and the rear of neutrophils."— Presentation transcript:

1 Mitochondria localize to both the front and the rear of neutrophils.
Mitochondria localize to both the front and the rear of neutrophils. (A) Random motility of neutrophils in the head mesenchyme of a 3 dpf larvae of Tg(lyzC:mitoDendra2)p14 crossed with Tg(lyzC:mCherry). (B) Quantification of fluorescence intensity along the indicated line (at 240 s). (C) Tg(lyzC:mitoDendra2)pu14 was crossed with Tg(lyzC:mCherry-H2B) to visualize mitochondria network relative to the nucleus. (D) Quantification of fluorescence intensity along the indicated line (at 140 s). Montages of one representative movie out of eight are shown. Arrows indicate the direction of cell migration. Scale bars: 5 µm. Wenqing Zhou et al. Dis. Model. Mech. 2018;11:dmm033027 © Published by The Company of Biologists Ltd

Download ppt "Mitochondria localize to both the front and the rear of neutrophils."

Similar presentations

Sec1p requires Boi1/2p for proper localization.

Sec1p requires Boi1/2p for proper localization.
TMZ and Ara-C treatment of slice co-cultures.

TMZ and Ara-C treatment of slice co-cultures.
The neuroepithelium of mid-neurulation mammalian embryos displays planar-polarised F-actin profiles. The neuroepithelium of mid-neurulation mammalian embryos.

The neuroepithelium of mid-neurulation mammalian embryos displays planar-polarised F-actin profiles. The neuroepithelium of mid-neurulation mammalian embryos.
Scanning electron microscopy analysis of EGK-I to -V chick embryos.

Scanning electron microscopy analysis of EGK-I to -V chick embryos.
CoC in practice. CoC in practice. The key input elements of CoC models are: (A) a microfluidic chip, (B) cancer cells, (C) additional cells (optional),

CoC in practice. CoC in practice. The key input elements of CoC models are: (A) a microfluidic chip, (B) cancer cells, (C) additional cells (optional),
Aggregation is not required for cytoplasmic relocalization induced by misfolding mutations. Aggregation is not required for cytoplasmic relocalization.

Aggregation is not required for cytoplasmic relocalization induced by misfolding mutations. Aggregation is not required for cytoplasmic relocalization.
BTN1 mRNA level in response to extracellular pH determined by comparative RT2PCR. BTN1mRNA level in response to extracellular pH determined by comparative.

BTN1 mRNA level in response to extracellular pH determined by comparative RT2PCR. BTN1mRNA level in response to extracellular pH determined by comparative.
Nephrogenesis in vitro can be rescued in 3D co-cultures by siRNA treatment of Renca cells. Nephrogenesis in vitro can be rescued in 3D co-cultures by siRNA.

Nephrogenesis in vitro can be rescued in 3D co-cultures by siRNA treatment of Renca cells. Nephrogenesis in vitro can be rescued in 3D co-cultures by siRNA.
Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.

Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.
Fig. 2. Proportion of motile objects and track length

Fig. 2. Proportion of motile objects and track length
An antagonistic relationship between myosin II and dynein controls bulk growth cone advance. An antagonistic relationship between myosin II and dynein.

An antagonistic relationship between myosin II and dynein controls bulk growth cone advance. An antagonistic relationship between myosin II and dynein.
A Drosophila cell culture model to study VAP(P58S) aggregation.

A Drosophila cell culture model to study VAP(P58S) aggregation.
Fig. 6. Cross-section of the stomach wall and spiral intestine of the embryo, stained with PAS. (A) Surface of the stomach wall (SW) and ingested material.

Fig. 6. Cross-section of the stomach wall and spiral intestine of the embryo, stained with PAS. (A) Surface of the stomach wall (SW) and ingested material.
OA and related amines modulate motility and length of schistosomula.

OA and related amines modulate motility and length of schistosomula.
Embryonic corneal defects in E18.5 AP-2β NCC KO mutant embryos.

Embryonic corneal defects in E18.5 AP-2β NCC KO mutant embryos.
Inflammation is associated with increased basal-cell plasticity in the Nkx3.1 mutant prostate. Inflammation is associated with increased basal-cell plasticity.

Inflammation is associated with increased basal-cell plasticity in the Nkx3.1 mutant prostate. Inflammation is associated with increased basal-cell plasticity.
Enterocytes fail to migrate consistently towards the villus tip in live APCMin/+ tissue. Enterocytes fail to migrate consistently towards the villus tip.

Enterocytes fail to migrate consistently towards the villus tip in live APCMin/+ tissue. Enterocytes fail to migrate consistently towards the villus tip.
Scanning EM shows cilia abnormalities in the neural tube.

Scanning EM shows cilia abnormalities in the neural tube.
Hipk induces cell spreading.

Hipk induces cell spreading.
Patient and control ONS cells had very large differences in gene expression. Patient and control ONS cells had very large differences in gene expression.

Patient and control ONS cells had very large differences in gene expression. Patient and control ONS cells had very large differences in gene expression.

Similar presentations

Ads by Google