Regulation of nerve growth and patterning by cell surface protein disulphide isomerase

Acceptance summary:

This excellent study reveals a mechanism for how growth of sensory and motor axons is restricted to the anterior half of each somite-derived sclerotome in the spinal cord, during generation of the segmented patterning of nerves during early peripheral nervous system development. The authors show that the cell surface protein disulphide isomerase contributes to such axonal segmentation by serving as an impenetrable barrier for growth cones in the posterior somite through acting on a nitric oxide/S-nitrosylation-dependent signal transduction pathway regulating the growth cone cytoskeleton, inducing axon growth cones to traverse the anterior half of each somite as they extend towards their body targets.

Decision letter after peer review:

Thank you for submitting your article "Regulation of nerve growth and patterning by cell surface protein disulphide isomerase" for consideration by eLife. Your article has been reviewed by three peer reviewers, and the evaluation has been overseen by a Reviewing Editor and Marianne Bronner as the Senior Editor. The following individual involved in review of your submission has agreed to reveal their identity: Ann Rajnicek (Reviewer #2).

The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.

Summary:

Your study on how the growth of sensory and motor axons are restricted to the anterior half of each somite-derived sclerotome, generating the segmented patterning of the early PNS, was viewed favorably by the reviewers. The demonstration of a key role for cell surface protein disulphide isomerase (PDI) via an NO-based mechanism in the establishment of such segmental axon patterning was deemed a major and important contribution. To ensure that the manuscript is accessible to the wide audience of eLife and to be clear even to developmental biologists, the reviewers and I ask that you insert a diagram in the first figure that would depict the somite arrangements and axon tracts, to set out the hypothesis, then a summary diagram in a final figure that would pull together the various strands of the results. Also, the reviewers call for examples of growth cone collapse and time course images, and for minor text modifications. I have left the reviews intact so that you can read the many positive comments on your study.

Essential revisions:

All of the revisions requested below are essential, and none call for performing new experiments.

Reviewer #1:

The restriction of the growth of sensory and motor axons to the anterior half of each somite-derived sclerotome, generating the segmented patterning of the early PNS, and the demonstration that this is due to contact repulsion exerted by the posterior sclerotome cells is one of the first and classic examples of this fundamental axon guidance mechanism. However, the molecular basis of segmental patterning is not understood. Here Cook and colleagues provide evidence for a key role for cell surface protein disulphide isomerase (PDI) via an NO-based mechanism in the establishment of segmental axon patterning and as such make a major and important contribution to our understanding.

Because they have previously shown that the lectin peanut agglutinin (PNA) binds to the posterior half sclerotome cells and that immobilised PNA depletes the collapse activity of the posterior sclerotome which is recovered by lactose elution, they subjected a major band in silver-stained SDS PAGE preparations of lactose elutes to tryptic digestion and mass spectrometry. This revealed numerous peptides distributed throughout PDIA1/P4HB, a member of the PDI family. They additionally showed that PDI staining appears in the posterior sclerotome shortly before the segmental emergence of sensory and motor axons. Importantly, they showed that in ovo microinjection of PDI siRNA, but not a scrambled control, disrupted the segmental patterning of early axons. As an alternative demonstration of the role of PDI, they microinjected a molecule that has been shown to specifically disrupt one of the active sites of PDI. Like PDI siRNA, this too disrupted segmental axon growth. To elucidate how PDI causes growth cone collapse, they investigated the potential involvement of an NO, based on the previous demonstration that NO causes growth cone collapse and that PDS catalyses NO entry by a transnitrosation mechanism. They showed in a DRG growth cone collapse assay that PDI (but not inhibited PDI) promotes NO donor-induced collapse. Moreover, somite extract-induced collapse was prevented by pre-treating DRG with an NOS inhibitor. Because S-nitrosylation of the MAPB1 light chain subunit LC1 has been shown to mediates calcium ionophore-induced growth cone collapse, they investigated whether a similar mechanism occurs in somite-induced growth cone collapse. Western blotting revealed that only one band, that corresponds to LC1, was S-nitrosylated in dissected somite strips and that S-nitrosylation of this band was prevented by an NOS inhibitor. Finally, they showed that PDI is expressed on mature astrocytes and that the growth cone collapsing activity of the grey matter of mature mammalian brain is blocked by inhibitors of PDI activity, suggesting that a similar mechanism operates in the CNS.

It is unfortunate that the chicken lacks suitable transgenetic tools, so well developed in mice, to demonstrate conclusively the role of PDI in segmental axon patterning. Nonetheless, the authors have done what is acceptable to show beyond reasonable doubt the role of PDI in segmental axon patterning and its mechanism of action in the developing chicken embryo. This is an important, far-reaching study. Many of the experiments are truly heroic given the very small quantity of tissue available. The results are well-controlled and logically presented and the paper is very well written. I have no major criticisms.

Reviewer #2:

This is a careful study in which a plethora of methodologies are used to dissect the molecular mechanisms by which cell surface protein disulphide isomerase underpins sensory axon segmentation of spinal neurons. It has important implications not just for developmental neuroscience but also for potential strategies to improve recalcitrant neuron growth in the mammalian central nervous system.

Overall the manuscript is well written and clearly organised into a sequence of logical experiments. It is evident that the authors have substantial expertise in the subject area. However, there are a few things that I would like to see addressed.

1) In terms of figure presentation, I think it would help enormously to have cartoons of the somite arrangements and the axon tracks coupled with the key molecular cues to set the stage for the study. That is, to describe the anatomy in a classical developmental biology/anatomy context. I don't think this is a minor point. eLife is a journal with a wide audience and the paper is written from the viewpoint of a hard-core developmental neuroscientist, which shows deep understanding of the specialist area, but which might make the paper inaccessible to a larger audience. A summary figure to set out the hypothesis in a first figure, coupled with a summary diagram in a final figure pulling together the various strands of the results would be incredibly useful. Both because of the wide range of specialist techniques used in the study and because there is a wider context in which the study could be interpreted- but there is a lot to digest from the text and the point is difficult to grasp in places.

2) The authors say that ….'co-injection of siRNA…rescued the normal segmented phenotype (Figure 2….)'. But looking at the data in the figure I think it is best to say that the phenotype was rescued partially.

3) A major point of the paper is that the authors have identified a growth cone collapse mechanism and they use a collapse assay (collected data are based on morphology) but there are no photographs of the growth cones in any of the figures. It would be useful to have images so the reader can get a feel for what 'collapse' looks like, especially with respect to soluble and contact mediated factors. For example, when the growth cones are challenged with soluble factors or liposomes: how do liposomes interact physically with filopodia in these cultures as compared to soluble factor influences on growth cone morphology (important because, as the authors state, a single filopodial contact can make all the difference)? They report time course data, so they must have time lapse images of growth cones as they collapse from which such measurements were made. These would be useful for the reader.

4) In a similar vein, given the importance of growth cone collapse and the role of the identified molecular mechanism on axon pathfinding I'm wondering why the authors did not include 'classical growth cone turning assay' or 'stripe assay' experiments. I am not necessarily requesting additional experiments, but if the authors have such data they would add to the study.

Reviewer #3:

In this interesting manuscript, Cook and colleagues provide a kind of closure to a long-standing question about patterning of metameric nerve growth in avian and mammalian embryos. Previous studies, many from the Keynes laboratory, showed that although both neural crest cells and motor and sensory axons traverse only the anterior half somite during outgrowth, the underlying molecular mechanisms that channel neural crest cell migration are distinct from those that channel axon extension. Here, they identify PDIA1/P4HB, a protein disulphide isomerase, as the cell surface activity required to prevent axons from entering the posterior half somite. They demonstrate that this PDI mediates axon repulsion by activating nitric oxide signaling, which elicits growth cone collapse. The also show that this PDI is the activity from adult brain extracts previously shown to mediate sensory axon growth cone collapse, and that this activity may emanate from astroglia.

This manuscript provides a satisfying answer to a question that has long been elusive. For the most part the data are very robust and well-documented. However, I suggest two types of improvements. First, other molecules, including ones described by the Keynes laboratory, are also implicated in preventing axons from entering the posterior half somite. This should be discussed. I think it would be very helpful to include a model figure that shows how PDI operates, as they describe in the Discussion, and also includes these other molecular mechanisms. Second, a number of figures could be improved.

1) Figure 1: It would be helpful to box the regions blown up in D-F.

2) Figure 1—figure supplement 1: It's very difficult to see what's going on in panel C. Asterisks or some other marker would help.

3) Figure 2: Is the loss of PDI random in these experiments? It looks like after siRNA it is gone in some somites and still present in others. Is this consistent? If so, how do you know whether it is effective?

4) Figure 2—figure supplement 2. It would be very helpful to show a blow up with comparisons for panel H.

[Editors' note: further revisions were suggested prior to acceptance, as described below.]

Thank you for submitting your article "Regulation of nerve growth and patterning by cell surface protein disulphide isomerase" for consideration by eLife. Your article has been reviewed by three peer reviewers, and the evaluation has been overseen by a Reviewing Editor and Marianne Bronner as the Senior Editor The following individual involved in review of your submission has agreed to reveal their identity: Alun M Davies (Reviewer #1).

The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.

We would like to draw your attention to changes in our revision policy that we have made in response to COVID-19 (https://elifesciences.org/articles/57162). Specifically, we are asking editors to accept without delay manuscripts, like yours, that they judge can stand as eLife papers without additional data, even if they feel that they would make the manuscript stronger. Thus the revisions requested below only address clarity and presentation.

Summary:

All three reviewers were enthusiastic about your study dissecting the molecular mechanisms by which the cell surface protein disulphide isomerase contributes to segmentation of sensory axons of spinal neurons. The study should appeal both to developmental biologists and those who study neuronal pathologies.

Reviewer 1 stated that "this is an excellent study that has been further improved by the revisions. The authors are to be congratulated on their achievements" and had no further comments at this stage. Reviewers 2 and 3 stated that the manuscript has been improved, and that you addressed the suggestions made and issues raised.

Essential revisions:

While reviewers 2 and 3 found that the changes to the figures, especially Figure 1, clarified the experimental outcomes and interpretation, there were three remaining amendments suggested:

1) In the figure legend for new Figure 1, you refer to '…mixed spinal nerves (yellow) but there is no yellow in the figure. Neither the arrow pointing to the nerve nor the nerve itself is yellow, so you may want to amend this.

2) New Figure 5 is also helpful, but reviewer 3 found the large red arrow at the bottom confusing. Is this meant to indicate retraction? If so, that should be described in the legend.

3) Reviewer 3 wonders why the you chose not to include an image of a collapsed growth cone, as suggested originally by reviewer 2. This would make the article more accessible to readers, without them having to look at additional references.