Fig. 4. Abdominal aortic aneurysm formation in zebrafish embryos following treatment with Angiotensin II or snuff extract. Abdominal aortic aneurysm formation.

Slides:



Advertisements
Similar presentations
Vegetal RNAs antagonise the dorsalising and BMP-inhibiting activity of Vrtn. Vegetal RNAs antagonise the dorsalising and BMP-inhibiting activity of Vrtn.
Advertisements

Rapid dilation of the abdominal aorta during infusion of angiotensin II detected by noninvasive high-frequency ultrasonography  Chiara Barisione, BSc,
Scanning electron microscopy analysis of EGK-I to -V chick embryos.
Il1b is required for the early and late recruitment of neutrophils but not macrophages. Il1b is required for the early and late recruitment of neutrophils.
Post-transcriptional deregulation of hnRNPH3 in sciatic nerve and neural cell bodies by loss of Ranbp2. Post-transcriptional deregulation of hnRNPH3 in.
Fig. 5 Local gel scaffold for T cell memory response.
Volume 20, Issue 21, Pages (November 2010)
Vascular endothelial growth factor enhances angiotensin II-induced aneurysm formation in apolipoprotein E-deficient mice  Edward Choke, PhD, MRCS, Gillian.
Volume 17, Issue 6, Pages (November 2016)
KIN-3 depletion leads to increased levels of centrosomal ZYG-1
CK2 is required for early cell divisions in C. elegans embryos
Effect of cxcr3.2 mutation on dissemination of local mycobacterial infection within 24 hpi. Effect of cxcr3.2 mutation on dissemination of local mycobacterial.
Fig. 6. crb_C mutant photoreceptor cells exhibit normal morphology.
Numerical analysis of cell morphology of tapetal cells in wild type.
Fig. 5. Prip silencing enhances the co-localization of GABARAP with insulin vesicles and β-tubulin.Co-localization of GABARAP (green) with insulin (red)
Fig. 4. Seeding density modulates cell shape in both cell types
Fig. 2. Proportion of motile objects and track length
Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle
Fig. 3. Lowered heart rate, ventricular dimensions, stroke volume and cardiac output in zebrafish embryos treated with cigarette smoke or snuff extracts.
Fig. 3. Knockdown of cited3 results in increased cell death but it does not affect proliferation.Embryos that are injected with the control MO (A–C), cited3.
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. 4. BMP and nodal induce invasion of metastatic and radial growth phase melanoma cells in human epidermal skin reconstructs. BMP and nodal induce invasion.
Fig. 1. Mitochondrial internalization in cardiomyocytes.
Fig. 1. E-cadherin localizes in nano-scale clusters.
Fig. 1. γ-Tubulin localizes in close proximity to centriole walls in interphase but within an extended PCM meshwork in mitosis.U2OS cells were fixed and.
Fig. 3. Genetic interactions between unc-53 and unc-6 and between unc-53 and unc-5 affect intracellular UNC-40::GFP localization.(A–H) Photomicrographs.
Impaired hemidesmosome formation in clint1 mutants.
Fig. 4. Non-autonomous rescue of puc expression in DME cells
Fig. 2. Ex vivo inducible knockout of PDCD2 in ESCs results in loss of S phase entry and increased p53.(A) Growth curve of inducible knockout and WT ESCs.
Combined treatment with LY and sunitinib rescued hypervascularization.
Elevated pAkt level in ptena−/−ptenb−/− mutants is suppressed by LY and to a lesser extent by sunitinib. Elevated pAkt level in ptena−/−ptenb−/−
Fig. 6. Comparison of Plk4 with Sas-6 localization
Fig. 7. Lhx1-RNAi reduces the eye size
Fig. 2. Centrosomal proteins display distinct localizations and radial distances from centriole walls.U2OS cells were fixed and stained with the indicated.
Fig. 5. UV reflections from the eye cup.
Fig. 2. Soluble sugar and organic acid levels with different K fertilization during fruit development. Soluble sugar and organic acid levels with different.
Fig. 7. Representative images of control (Cas9+GFP) and Cas9+gRNA+GFP co-injected embryos on day 4 of culture, showing nuclear-imported GFP (green) and.
Fig. 4. Co-immunostaining of nocodazole or ASNase treated RPE-1 cells with anti-hASNS and anti-alpha tubulin showed defect in both mitotic spindle formation.
Delayed formation of sensory hair cells in dlx3b/4b-deficient embryos
BMP signalling is dispensable for early gastruloid patterning.
Fig. 5. Combination of SAHA and ML produces augmented suppression of cellular proliferation with impaired cell cycle progression, enhanced apoptotic.
Fig. 3. Weak interaction between E-cadherin and N-cadherin null cells
The idefix phenotype first becomes visible during metamorphosis
Fig. 8. The morphology of the ventral nerve cord in Ror-Myc overexpressing embryos is normal. The morphology of the ventral nerve cord in Ror-Myc overexpressing.
prdm1a is co-expressed with foxd3 and tfap2a at the NPB
Transbilayer distribution of cholesterol in the plasma membrane is defective in staurosporine-treated cells. Transbilayer distribution of cholesterol in.
EpiDEG efficiently degrades GFP-tagged proteins that localize to different subcellular localizations. epiDEG efficiently degrades GFP-tagged proteins that.
Fig. 4. Perinuclear dynein regulators are not required for primary ciliogenesis.RPE cells were transfected with siRNA and either nocodazole-treated, fixed,
Sox2 regulates dental epithelial stem cell proliferation and differentiation. Sox2 regulates dental epithelial stem cell proliferation and differentiation.
Depleting CK2 restores centrosomal ZYG-1 levels in zyg-1(it25) embryos
Folic acid increases apical junctional pMLCK localization in vivo
Fig. 2. Non-homogeneous subcellular distribution of Vangl2 along the anteroposterior axis. Non-homogeneous subcellular distribution of Vangl2 along the.
Fig. 2. iPSCs produce functional osteoblasts.
Effects of Chd1-knockdown on Hmgpi and Klf5 expression
Ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis. ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis.
Chd1 expression and CHD1 localization during mouse preimplantation development. Chd1 expression and CHD1 localization during mouse preimplantation development.
Global cell proliferation replenishes epidermal cells.
Overexpression of cyp7a1 in the liver ameliorates tumor-induced liver inflammation. Overexpression of cyp7a1 in the liver ameliorates tumor-induced liver.
Fig. 2. Expression of Cx43 mutant T154A resulted in non-radial spreading and formation of protrusions in J558µm3 cells spreading in response to BCR signaling.(A)
Activation of glial cells.
Fig. 1. Rnd2 and Rnd3 induce stress fibres whereas Rnd1 reduces stress fibres in endothelial cells.(A) Rnd mRNAs are expressed in HUVECs. Total RNA was.
Fig. 3. MO-mediated smc3 knockdown results in reduced regenerate length, segment length and cell proliferation. MO-mediated smc3 knockdown results in reduced.
Fig. 5. EGL-20 inhibits anterior and posterior orientation of UNC-40 asymmetric localization and the formation of axons from these sites.(A–D) HSN neurons.
Nutrient availability regulates growth of the X. laevis optic tectum.
Fig. 1. Expression of a Ror-eGFP fusion protein under control of the endogenous Ror promoter in Drosophila embryos. Expression of a Ror-eGFP fusion protein.
mip120 null egg chambers have a condensed nurse cell DNA phenotype
Fig. 2. Defective development of lymphatic vessels in zebrafish embryos treated with cigarette smoke extract or snuff extract. Defective development of.
Fig. 5. Co-expression analyses of disease mutations in YFP-RPGRIP1α1 with wild-type RFP-RPGR1–19 or RFP-RPGRORF15 in COS7 cells.YFP-RPGRIP1α1 with disease-associated.
Phenotypic analysis of the CNS in mutants for Ror, otk and otk2
Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP
Presentation transcript:

Fig. 4. Abdominal aortic aneurysm formation in zebrafish embryos following treatment with Angiotensin II or snuff extract. Abdominal aortic aneurysm formation in zebrafish embryos following treatment with Angiotensin II or snuff extract. (A) Confocal micrographs of the central trunk region in fli1a:EGFP embryos at 4 days post-fertilization (dpf) either non-treated (control), injected at the 1-cell stage with 50 ng angiotensin II (AngII) in the yolk, or treated with cigarette smoke extract (CS) at 1:30 dilution or snuff extract at 1:50 dilution from the 2 dpf stage. The aorta is highlighted in a magnified image under the overview image and the abdominal (anterior) and distal (posterior) parts of the aorta further magnified in the left and right images, respectively, under the isolated aorta image. Red dots outline the aortic wall. Scale bars: 100 µm, 50 µm and 50 µm in the overview, aorta highlight and posterior aorta highlight images, respectively. (B) Quantification of the average aorta diameter in the abdominal region (anterior aorta images shown in A) of control zebrafish embryos during development. n=20, 9, 20, 19 and 12 embryos at 24, 48, 72, 98 and 120 hpf, respectively. *P<0.05, ***P<0.001. (C) Quantification of the average aorta diameter in the abdominal region (anterior aorta images shown in A) of zebrafish embryos treated with CS, snuff or AngII as in A. n=19, 7, 7 and 13 in the control, CS, Sn and AngII groups respectively. **P<0.01, ***P<0.001. All experiments were repeated twice with similar results. Results are shown as means±s.e.m. and statistical evaluation was done using Student’s two-tailed t-test assuming equal variance between the groups. Maggie Folkesson et al. Biology Open 2016;5:970-978 © 2016. Published by The Company of Biologists Ltd