This work was funded by a BBSRC grant to MEP (BB/H010297/1), a BBSRC quota studentship to SAR, and an MRC studentship to SWF.

Ethics statement: Animal experiments were done under a UK Home office licence to MEP and the experiments carried out was approved by the University of York ethics committee in compliance with the ARRIVE (Animal Research: Reporting of In Vivo Experiments) guidelines. (https://www.nc3rs.org.uk/arrive-guidelines).
1. Strategy to Generate Fluorescently Tagged Ligands
Below is an example protocol for subcloning Wnt8a-HA and eGFP into pCS2, in order to produce the ...

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The authors have no competing financial interests.

An essential part of this protocol is generating biologically active ligands that are normally processed, secreted, and able to elicit a response in the receiving cell, despite having a fluorescent moiety attached. It is critical to establish that the fluorescently-tagged gene product is biologically active using an appropriate assay. For Shh-GFP, the ability to activate the expression of ptc1 was confirmed16. Wnt8a has a remarkably potent ability to induce a secondary axis when expressed in a single ...

During early embryonic development, cells are progressively committed to follow specific lineages of differentiation: this means a group of totipotent (or pluripotent) cells become gradually restricted to establishing populations of progenitor cells determined to give rise to one cell type. Cell-cell signalling is central to the regulation of lineage specification during embryonic development. Manipulation of these signals will be required to direct stem cells toward particular fates to support novel medical treatments.
A relatively small number of signalling pathways are reiterated during development, including pathways responding to the TGF superfamily (nodals and BMPs)1-2, FGFs3, Wnts4, and Hedgehogs5. These secreted proteins bind receptors present on the cell membrane to activate signal transduction thereby altering gene expression and/or cell behaviour. The tight regulation of cell signalling is essential for cell lineage specification and normal development. While the cross-talk among these pathways is important in determining cell fate, a single ligand can itself elicit distinct responses at different concentrations. Morphogen gradients were described over 100 years ago as a theory to explain how different cell types can derive from a field of cells6. Signalling molecules produced by one group of cells may diffuse over a certain range, decreasing in concentration with a greater distance from the source. Cells exposed to the signal will respond to the local concentration at their position in the field of cells, with cells at distinct positions responding differently to different levels of the signal. Evidence for the existence of morphogens comes from studies of the early Drosophila embryo7 and the wing disc8, as well as the vertebrate limb9 and neural tube10.
Methods are needed to investigate how morphogen gradients are established and to identify other molecules important in regulating these gradients. Elegant experiments using immunohistochemistry to visualise endogenous proteins in vivo in the context of different genetic backgrounds have been used to investigate morphogen gradients11-12. However, good antibodies and specific mutants are not always available, so we describe here a protocol using overexpression of fluorescent ligands in Xenopus, to provide an alternative, simple method to dissect how exogenous gene products can influence distribution of ligands across a field of cells. Xenopus laevis provides an excellent system to undertake these types of experiments as their embryos develop externally so they are accessible at the earliest stages. Their large size (1-1.5mm in diameter) simplifies microinjection and surgical manipulation and by blastula stages the cells are easy to image as they are still relatively big (about 20&#181;m across). Overexpression studies in Xenopus are simple to do: mRNA injected into the early embryo can be targeted to particular cells and is efficiently translated.
The fluorescently tagged Wnt8a/Wnt11b-HA-eGFP constructs were generated using pCS2 Wnt8a-HA13, pCS2 Wnt11b-HA14 and eGFP. The HA peptide is important to include, not only to provide an additional molecular tag, but also because it is thought to act as a spacer separating the Wnt and eGFP proteins allowing both gene products to function. The construct used for the visualisation of Shh was previously used to generate a transgenic mouse expressing a Shh-eGFP fusion protein15; this was kindly provided by Andy McMahon. Importantly, the GFP tag for all the constructs is cloned 3&#8217; to the signal sequence such that it is retained after processing. It is also essential to ensure that the final protein includes sequences required for modifications, such the addition of lipids as is the case for Shh and Wnt ligands.The cDNAs were subcloned into the pCS2+ expression vector which is optimised for the prodution of synthetic mRNA; it includes an SP6 promoter and polyadenylation signal (http://sitemaker.umich.edu/dlturner.vectors).
The work described here provides a simple protocol for comparing the secretion and diffusion of fluorescently tagged Wnt and Shh tagged ligands. By injecting defined amounts of synthetic mRNA, the protocol circumnavigates any problems associated with variable expression from different vectors using different promoters. These methods have recently been applied to investigate the effects of the heparan sulfate endosulfatase Sulf1 on Shh-eGFP and Wnt8a/Wnt11b-HA-eGFP secretion and diffusion in Xenopus16-17.

<table>
	<tbody>
		<tr>
			<td>Agarose</td>
			<td>Melford</td>
			<td>MB 1200</td>
			<td></td>
		</tr>
		<tr>
			<td>Ammonium acetate</td>
			<td>Ambion</td>
			<td>From Megascript SP6 Kit AM 1330</td>
			<td></td>
		</tr>
		<tr>
			<td>Bicarbonate</td>
			<td>VWR International</td>
			<td>RC-091</td>
			<td></td>
		</tr>
		<tr>
			<td>Calcium nitrate</td>
			<td>Sigma</td>
			<td>C13961</td>
			<td></td>
		</tr>
		<tr>
			<td>Cap analog (m7G(5&#39;))</td>
			<td>Applied Biosystems</td>
			<td>AM 8050</td>
			<td></td>
		</tr>
		<tr>
			<td>Chloroform</td>
			<td>Sigma</td>
			<td>C 2432</td>
			<td></td>
		</tr>
		<tr>
			<td>&#160;L-Cysteine hydrochloride monohydrate</td>
			<td>Sigma</td>
			<td>C7880</td>
			<td></td>
		</tr>
		<tr>
			<td>dNTPs</td>
			<td>Invitrogen</td>
			<td>18427-013</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethylenediaminetetraacetic acid (EDTA)</td>
			<td>Sigma</td>
			<td>O3690</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethanol</td>
			<td>VWR International</td>
			<td>20821.33</td>
			<td></td>
		</tr>
		<tr>
			<td>Ficoll 400</td>
			<td>Sigma</td>
			<td>F 4375</td>
			<td></td>
		</tr>
		<tr>
			<td>Fiji image J software</td>
			<td>N/A</td>
			<td>N/A</td>
			<td>Free download http://fiji.sc/Fiji</td>
		</tr>
		<tr>
			<td>Gentamycin</td>
			<td>Melford</td>
			<td>G 0124</td>
			<td></td>
		</tr>
		<tr>
			<td>Glacial acetic acid</td>
			<td>Fisher Scientific</td>
			<td>A/0400/PB17</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass cover slips, No.1.5&#160;</td>
			<td>Scientific Laboratory Supplies</td>
			<td>22X22-SGJ3015. 22X50-SGJ3030&#160;</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass needle puller</td>
			<td>Narishige</td>
			<td>Narishige PC -10</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass pull needles</td>
			<td>Drummond Scientific</td>
			<td>3-000-203-G/X</td>
			<td></td>
		</tr>
		<tr>
			<td>Human chronic gonadotropin (HCG)</td>
			<td>Intervet</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Isopropanol</td>
			<td>Fisher Scientific</td>
			<td>P/7500/PB17</td>
			<td></td>
		</tr>
		<tr>
			<td>Lithium chloride (LiCl)</td>
			<td>Sigma</td>
			<td>L-7026</td>
			<td></td>
		</tr>
		<tr>
			<td>LSM710 and Zen software (2008-2010)</td>
			<td>Carl Zeiss</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Matlab software</td>
			<td>Mathworks</td>
			<td></td>
			<td>http://uk.mathworks.com/</td>
		</tr>
		<tr>
			<td>Molecular grade water&#160;</td>
			<td>Fisher Scientific</td>
			<td>BP 2819-10</td>
			<td></td>
		</tr>
		<tr>
			<td>Nail varnish&#160;</td>
			<td>Boots</td>
			<td>Bar code 3600530 373048</td>
			<td></td>
		</tr>
		<tr>
			<td>Spectrophotometer</td>
			<td>Lab.tech International</td>
			<td>ND-1000 / ND8000</td>
			<td></td>
		</tr>
		<tr>
			<td>Petri dish (55mm)</td>
			<td>VWR International</td>
			<td>391-0865</td>
			<td></td>
		</tr>
		<tr>
			<td>Phenol-chloroform</td>
			<td>Sigma</td>
			<td>P3803</td>
			<td></td>
		</tr>
		<tr>
			<td>Photoshop software</td>
			<td>Adobe</td>
			<td>N/A</td>
			<td>http://www.photoshop.com/products</td>
		</tr>
		<tr>
			<td>High fidelity DNA polymerase and buffers&#160;</td>
			<td>Biolabs</td>
			<td>M0530S&#160; Buffer - M0531S</td>
			<td></td>
		</tr>
		<tr>
			<td>Potassium chloride (KCl)</td>
			<td>Fisher Scientific</td>
			<td>P/4280/53</td>
			<td></td>
		</tr>
		<tr>
			<td>PVC insulation tape</td>
			<td>Onecall</td>
			<td>SH5006MPK</td>
			<td></td>
		</tr>
		<tr>
			<td>Gel extraction kit&#160;</td>
			<td>Qiagen</td>
			<td>S28704</td>
			<td></td>
		</tr>
		<tr>
			<td>Restriction enzymes buffers</td>
			<td>Roche</td>
			<td colspan="2">SuRE/CUT Buffer Set 11082 035 001</td>
		</tr>
		<tr>
			<td>RNAse-free DNAse</td>
			<td>Promega</td>
			<td>ME10A</td>
			<td></td>
		</tr>
		<tr>
			<td>Steel back single edge blades</td>
			<td>Personna</td>
			<td>66-0403-0000</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium chloride (NaCl)</td>
			<td>Fisher Scientific</td>
			<td>27810.364</td>
			<td></td>
		</tr>
		<tr>
			<td>SP6 transcription kit</td>
			<td>Ambion</td>
			<td>AM1330</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass slides</td>
			<td>Thermo Fisher</td>
			<td>SHE 2505</td>
			<td></td>
		</tr>
		<tr>
			<td>Tris base</td>
			<td>Invitrogen</td>
			<td>15504-020</td>
			<td></td>
		</tr>
		<tr>
			<td>Tungsten needles</td>
			<td>N/A</td>
			<td>N/A</td>
			<td>homemade</td>
		</tr>
		<tr>
			<td>Zen lite software</td>
			<td>Carl Zeiss</td>
			<td>N/A</td>
			<td>Free download&#160; http://www.zeiss.co.uk/microscopy/en_gb/downloads/zen.html</td>
		</tr>
	</tbody>
</table>

using confocal analysis of xenopus laevis to investigate modulators of wnt and shh morphogen gradients

This protocol describes a method to visualise ligands distributed across a field of cells. The ease of expressing exogenous proteins, together with the large size of their cells in early embryos, make Xenopus laevis a useful model for visualising GFP-tagged ligands. Synthetic mRNAs are efficiently translated after injection into early stage Xenopus embryos, and injections can be targeted to a single cell. When combined with a lineage tracer such as membrane tethered RFP, the injected cell (and its descendants) that are producing the overexpressed protein can easily be followed. This protocol describes a method for the production of fluorescently tagged Wnt and Shh ligands from injected mRNA. The methods involve the micro dissection of ectodermal explants (animal caps) and the analysis of ligand diffusion in multiple samples. By using confocal imaging, information about ligand secretion and diffusion over a field of cells can be obtained. Statistical analyses of confocal images provide quantitative data on the shape of ligand gradients. These methods may be useful to researchers who want to test the effects of factors that may regulate the shape of morphogen gradients.

Confocal analysis of animal cap explants expressing fluorescently tagged proteins provides an effective system for visualising ligand distribution under different experimental conditions. In one example, the distribution of GFP tagged Shh is shown (Figure 1). At the 2-cell stage, Xenopus embryos are injected into both cells with either with a control mRNA or with mRNA coding for Sulf1, an enzyme that modifies cell surface heparan sulfate and influences the Shh morphogen gradient16. Th...

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Using Confocal Analysis of Xenopus laevis to Investigate Modulators of Wnt and Shh Morphogen Gradients

The manuscript here provides a simple set of methods for analysing the secretion and diffusion of fluorescently tagged ligands in Xenopus. This provides a context for testing the ability of other proteins to modify ligand distribution and allowing experiments that may give insight into mechanisms regulating morphogen gradients.

Using Confocal Analysis of Xenopus laevis to Investigate Modulators of Wnt and Shh Morphogen Gradients

This protocol describes a method to visualise ligands distributed across a field of cells. The ease of expressing exogenous proteins, together with the ...

using-confocal-analysis-xenopus-laevis-to-investigate-modulators-wnt

Research

JoVE Journal

Developmental Biology

11.0K visualizações.  The Bateson Centre, University of Sheffield.  O manuscrito aqui fornece um simples conjunto de métodos que permitam analisar a secreção e difusão de ligantes marcados fluorescentes em Xenopus. Isto proporciona um contexto para testar a capacidade de outras proteínas para modificar a distribuição de ligando e permitindo experiências que podem dar uma visão sobre os mecanismos que regulam a gradientes de morfogénio. 