BMP signalling is dispensable for early gastruloid patterning.

Slides:



Advertisements
Similar presentations
inhibits BMP signalling.
Advertisements

Mitochondria localize to both the front and the rear of neutrophils.
Sec1p requires Boi1/2p for proper localization.
Vegetal RNAs antagonise the dorsalising and BMP-inhibiting activity of Vrtn. Vegetal RNAs antagonise the dorsalising and BMP-inhibiting activity of Vrtn.
Scanning electron microscopy analysis of EGK-I to -V chick embryos.
Fig. 4. Specific versus nonspecific NP accumulation.
Arc expression increases H4K12Ac levels.
KIN-3 depletion leads to increased levels of centrosomal ZYG-1
Cortical NuMA enrichment upon Plk1 inhibition is dynein independent.
Numerical analysis of cell morphology of tapetal cells in wild type.
Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial cells using live-imaging. Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial.
Aggregation is not required for cytoplasmic relocalization induced by misfolding mutations. Aggregation is not required for cytoplasmic relocalization.
Retinoic acid sentinels in live embryos and responding to exogenous RA in half-embryo cultures. Retinoic acid sentinels in live embryos and responding.
Fig. 8. CCA and ChQ treatment induce accumulation of F-actin rings.
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
Fig. 4. smc3 regulates the expression of cx43 in regenerating fins.
Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.
Fig. 5. Differentiated cells sort to the outer layer, regardless of E- or N-cadherin status.Wildtype and mutant ES cells were distinguished by GFP expression.
Fig. 4. Seeding density modulates cell shape in both cell types
Altered oligodendrocyte progenitor cell (OPC) marker protein expression in two white matter regions of ShhΔFP/ΔFP and SmoΔNT/ΔNT embryos at E15.5. Altered.
Fig. 4. A primary screen based on scrape closure
Embryonic corneal defects in E18.5 AP-2β NCC KO mutant embryos.
Fig. 1. Mitochondrial internalization in cardiomyocytes.
Fig. 5. Expression of either dFMRP or human FMRP does not induce eIF2α phosphorylation.(A) Analysis of eIF2α phosphorylation upon dFMRP expression. Expression.
Fig. 3. Inactivation of the Wnt/β-catenin signaling pathway inhibited cell proliferation and induced apoptosis in A549 and SPC-A-1 cells. Inactivation.
Fig. 1. E-cadherin localizes in nano-scale clusters.
Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.
The initial targeting of Sec61b mRNA to the ER is partially dependent on ribosomes and translation. The initial targeting of Sec61b mRNA to the ER is partially.
Kinetics of induced and non-induced AR, and its relationship to cell death and motility. Kinetics of induced and non-induced AR, and its relationship to.
Fig. 5. The bulk of Cep135 localizes distantly from Sas-6 and STIL
Fig. 6. Comparison of Plk4 with Sas-6 localization
Fig. 2. Morphological analysis of acentriolar mitotic spindles
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.
Simultaneous perturbations to shuttling result in defects in the Dl gradient and in the sna domain. Simultaneous perturbations to shuttling result in defects.
Fig. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent.
Comparison ofMyc-induced zebrafish liver tumors with different stages of human HCC and seven mouse HCC models. Comparison ofMyc-induced zebrafish liver.
Wnt/β-catenin inhibition delays but does not inhibit T/Bra::GFP expression. Wnt/β-catenin inhibition delays but does not inhibit T/Bra::GFP expression.
Axial organisation of gastruloids.
Nodal signalling is absolutely required for T/Bra induction and correct patterning. Nodal signalling is absolutely required for T/Bra induction and correct.
Involvement of IRS-1 in L-783,281–stimulated increases in [Ca2+]i and exocytosis. Involvement of IRS-1 in L-783,281–stimulated increases in [Ca2+]i and.
ArfGAP1 expression alters GBF1 recruitment to Golgi membranes.
Effect of the plastid translation inhibitor Spec on LR development
Effects of fAS stimulation on cathepsin-B activity, mitochondrial quality and microglial cell survival after autophagy inhibition. Effects of fAS stimulation.
EpiDEG efficiently degrades GFP-tagged proteins that localize to different subcellular localizations. epiDEG efficiently degrades GFP-tagged proteins that.
Fig. 9. Loss of the cholinergic receptor subunit Chrna6 does not alter the development and organization of the mdDA system.(A) In situ hybridization experiments.
Depleting CK2 restores centrosomal ZYG-1 levels in zyg-1(it25) embryos
Wnt/β-catenin signalling stabilises and enhances spontaneous symmetry-breaking and polarisation events in gastruloids. Wnt/β-catenin signalling stabilises.
Deletion of Sox2 in adult mice inhibits incisor regeneration.
Differential optogenetic stimulation of Rac and Cdc42 induces lamellipodia and directed migration on a FN substrate. Differential optogenetic stimulation.
Ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis. ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis.
dcn1-deletion results in attenuated cohesin cleavage at anaphase
Defective MEK-Erk1/2 kinase activation in RIAM-depleted cells accounts for their impaired FA disassembly. Defective MEK-Erk1/2 kinase activation in RIAM-depleted.
Global cell proliferation replenishes epidermal cells.
VEGF stimulation together with inhibition of mTORC1 induces endothelial cell elongation independently of Foxo1. VEGF stimulation together with inhibition.
Altered intracellular distributions of acetylated α-tubulin, mitochondria and peroxisomes. Altered intracellular distributions of acetylated α-tubulin,
Nutrient availability regulates Xenopus laevis tadpole growth and progression through developmental stages. Nutrient availability regulates Xenopus laevis.
Fig. 1. Cell adhesion molecule expression and the aggregation of wildtype and mutant ES cells.(A) Wildtype (WT), E-cadherin null (9J), and N-cadherin null.
Nutrient availability regulates growth of the X. laevis optic tectum.
The BRCA1 aggregates exclude large nuclear structures.
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.
Depletion of COPI protein inhibits cis to trans cisternal maturation.
GCaMPs in Drosophila. GCaMPs in Drosophila. A, Schematic of larval NMJ preparation, and close-up of Type 1b boutons from muscle 13 (segments A3–A5) used.
Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.
Sensory neurons grow and downregulate UCHL1 expression levels during postnatal maturation. Sensory neurons grow and downregulate UCHL1 expression levels.
Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP
Two REMS-like iterations demonstrating common patterns of rapid brightness changes of skin patterning. Two REMS-like iterations demonstrating common patterns.
2DG suppresses of lamellipodia and filopodia and causes disorganization of F-actin filaments in murine endothelial cells. 2DG suppresses of lamellipodia.
Example of swimming trajectories from three groups of fish from three different weeks along with the extracted behavioral parameters. Example of swimming.
Distinct mitochondrial membrane potential, ATP-to-ADP ratio and NAD(P)H responses to glucose and methylsuccinate. Distinct mitochondrial membrane potential,
Presentation transcript:

BMP signalling is dispensable for early gastruloid patterning. BMP signalling is dispensable for early gastruloid patterning. (A) T/Bra::GFP gastruloids stimulated with Chi (48-72 h) AA following a 24 h pulse of either vehicle (top), BMP4 (middle) or DMH1 (bottom; n=12, 13 and 13 at 120 h, respectively), an inhibitor of BMP signalling between 24 and 48 h AA. Normalised fluorescence traces shown per condition (A) with corresponding fluorescence and shape descriptor quantification (B). Inhibition of BMP signalling by DMH1 or activation by BMP4 (24-48 h AA) does not alter the initial patterning of gastruloids; BMP treatment at this time has minimal effect on the subsequent patterning. (C) Gastruloids imaged at 120 h by wide-field microscopy following 24-48 h of vehicle or BMP4 stimulation (pink horizontal box) followed by either vehicle, Chi or BMP4 as indicated (blue horizontal box) between 48 and 72 h AA (n=16 per condition). (D) Stimulation schematic. BMP4 is unable to substitute for Chi in terms of the elongation and patterning of T/Bra, and its sustained expression over time (refer to Fig. S10 for further details and statistical analysis). Scale bar: 200 µm. David A. Turner et al. Development 2017;144:3894-3906 © 2017. Published by The Company of Biologists Ltd