Gastrulation occurs in multiple phases at two distinct sites in Latrodectus and Cheiracanthium spiders
© Edgar et al. 2015
Received: 11 August 2015
Accepted: 5 October 2015
Published: 21 October 2015
The longstanding canonical model of spider gastrulation posits that cell internalization occurs only at a unitary central blastopore; and that the cumulus (dorsal organizer) arises from within the early deep layer by cell–cell interaction. Recent work has begun to challenge the canonical model by demonstrating cell internalization at extra-blastoporal sites in two species (Parasteatoda tepidariorum and Zygiella x-notata); and showing in Zygiella that the prospective cumulus internalizes first, before other cells are present in the deep layer. The cell behaviors making up spider gastrulation thus appear to show considerable variation, and a wider sampling of taxa is indicated.
We evaluated the model in three species from two families by direct observation of living embryos. Movements of individual cells were traced from timelapse recordings and the origin and fate of the cumulus determined by CM-DiI labeling. We show that there are two distinct regions of internalization: most cells enter the deep layer via the central blastopore but many additional cells ingress via an extra-blastoporal ring, either at the periphery of the germ disc (Latrodectus spp.) or nearer the central field (Cheiracanthium mildei). In all species, the cumulus cells internalize first; this is shown by tracing cells in timelapse, histology, and by CM-DiI injection into the deep layer. Injection very early in gastrulation labels only cumulus mesenchyme cells whereas injections at later stages label non-cumulus mesoderm and endoderm.
We propose a revised model to accommodate the new data. Our working model has the prospective cumulus cells internalizing first, at the central blastopore. The cumulus cells begin migration before other cells enter the deep layer. This is consistent with early specification of the cumulus and suggests that cell–cell interaction with other deep layer cells is not required for its function. As the cumulus migrates, additional mesendoderm internalizes at two distinct locations: through the central blastopore and at an extra-blastoporal ring. Our work thus demonstrates early, cell-autonomous behavior of the cumulus and variation in subsequent location and timing of cell internalization during gastrulation in spiders.
KeywordsGastrulation Morphogenesis Arthropod Chelicerate Arachnid Spider
Spiders are an emerging system to probe arthropod development and the developmental origins of arthropod diversity . As representatives of Chelicerata, the sister group to all other extant arthropod lineages , spiders are well positioned for comparative analysis. They are tractable in the laboratory, and much recent work has illuminated aspects of spider development such as axial (e.g. [3–5]), segmental (e.g. [6–8]), and regional patterning (e.g. [9, 10]). A relatively neglected area is the cell rearrangements driving gastrulation. Gastrulation is a key event in early development that converts the simple symmetry of the egg into the more complex symmetries of the later embryo. Subsequent morphogenesis builds on the outcome of gastrulation. While gastrulation varies widely across major taxonomic groups, it is not known whether modifications to gastrulation over smaller evolutionary time scales carry phylogenetic signal.
Spider development begins as early cleavage nuclei migrate from the interior to form a monolayered blastoderm that evenly covers the yolk. Despite a superficial resemblance to the Drosophila syncytial blastoderm, spider embryos exhibit a form of total cleavage from at least the 16-cell stage, as demonstrated by three lines of evidence: older histological work described ‘yolk pyramids’ suggestive of yolk compartmentation ; injected fluorochrome-conjugated dextran does not diffuse beyond these compartment boundaries in P. tepidariorum ; and similar pyramidal compartments appear in SEM of fractured C. salei embryos . In some species, most of the blastoderm cells migrate towards one hemisphere to form a distinct germ disc. At these early stages, the geometry of the spider embryo is analogous to that of the chicken, in that the embryo arises from a thin disc of cells resting on a larger yolk mass.
Gastrulation begins near the center of the radially symmetrical germ disc (Fig. 1). As cells internalize, the multilayered portion of the germ disc appears opaque and is commonly termed the ‘primitive plate’ or ‘primary thickening’ [14, 24]. Two distinct populations of internalized cells compose the deep layer in every spider embryo studied to date: a dorsal organizer termed the ‘cumulus’ and a presumably mixed population of prospective mesoderm and endoderm cells (mesendoderm). The canonical model of spider development asserts that these two cell populations become specified only after significant internalization of a deep layer.
The cumulus is a small group of mesenchymal cells that actively migrates to the prospective dorso-posterior edge of the germ disc. The arc defined by the blastopore (posterior) and the cumulus’s endpoint (dorsal) effectively implies all body axes. The cumulus is necessary and sufficient to establish the body axes: surgical extirpation results in radialized embryos and ectopic cumulus implantation duplicates the body axis [11, 19]. Furthermore, its cells express decapentaplegic (dpp) mRNA , and knockdown of dpp results in severe axial defects including radialization of the dorsal–ventral axis . The majority of cells in the deep layer is not part of the cumulus and will form the bulk of the mesoderm and endoderm. In fixed embryos, the cumulus is morphologically distinct. Seen by scanning electron microscopy, the cumulus deep cells of P. tepidariorum appear almost spherical . In histological sections from other species, their appearance is similar: cumulus cells are large, round, and often vacuolated or relatively lightly stained [25, 26].
Cell rearrangements transform the original disc into an elongated germ band as the cells along the cumulus’s path spread out. The newly thinned area is termed the dorsal field, and will form extraembryonic tissues. The multilayered area (light color in Fig. 1e) comprises many more cells and will form the germ band. The germ band then splits longitudinally along the ventral midline to form the ventral sulcus and its two halves (the right and left sides of the body) migrate to opposite sides of the yolk. This process is called inversion, and occurs in most spiders and one other arachnid order . Subsequent ventral and dorsal closure movements complete the spiderling.
The canonical model of gastrulation is valuable because it provides a shared framework for research; however, variation from this model among spider species would indicate that the evolution of different gastrulation strategies can happen over smaller time scales. Furthermore, there remain important unanswered questions about the basics of spider gastrulation. There are two questions that interest us most: (1) Is the central blastopore the only point of cell internalization? Multiple sites of internalization would violate the canonical model, and the data in the literature are somewhat contradictory, see below. (2) What is the timing of internalization of the cumulus cells relative to the rest of the deep layer? This is interesting from the point of view of cell specification: if the cumulus arises before other cells internalize, then it is likely to be already specified rather than forming as a result of cell–cell interaction within the deep layer.
Whether there are multiple sites of gastrulation in spiders has been a point of contention in historical and contemporary literature. Histological, molecular, and lineage tracing evidence support cell internalization at both the center and the peripheral rim of the germ disc. Rempel showed drawings of histological sections with an apparent accumulation of cells at the rim of the germ disc in the black widow spider, Latrodectus mactans , which confirmed earlier work by Montgomery . In P. tepidariorum, twist-expressing cells in the deep layer were shown to originate at the periphery of the germ disc . However, Wolff and Hilbrant  found no evidence of internalization at the germ disc rim in C. salei. In the silver-sided sector spider, Zygiella x-notata, Chaw et al.  used timelapse video to document cell behavior of the superficial cells of the germ disc and likewise found no internalization at the germ disc rim. To evaluate whether or not internalization at extra-blastoporal sites is a general phenomenon of spider development, cell tracing in living embryos is required. Static observations alone—histological or gene expression patterns—cannot reveal the spatial origin of actively migrating cells. For example, deep cells at the rim of the germ disc could arise from the central blastopore and migrate to the periphery .
For this paper, we used high-resolution timelapse videography, direct labeling of cells with CM-DiI, and improved histology to evaluate gastrulation in three spider species. In Latrodectus spp. (L. mactans and L. geometricus, the brown widow spider) and in the yellow sac spider, Cheiracanthium mildei, the cells of the cumulus internalize early and separately from the primary mesendoderm. We document active internalization at the rim of the germ disc in Latrodectus spp. and in a region outside the central blastopore in C. mildei. The timing of cumulus formation is consistent with a cell-autonomous mechanism for its formation. Our results provide the most detailed evaluation of cell behavior during gastrulation yet achieved in spiders, and suggest modifications to the canonical model.
Organisms Adult Cheiracanthium mildei and their egg sacs were collected locally. Females were housed individually at room temperature (22°–24 °C) with a 12-h light cycle, and fed crickets to satiation. Spiders were occasionally mated in the lab. Egg masses contained about 30–100 eggs, each 0.7–0.9 mm in diameter. Adult Latrodectus mactans and Latrodectus geometricus were purchased from SpiderPharm and were housed and fed similarly to C. mildei. The spiders were mated immediately before shipping by SpiderPharm, for which we are very grateful. Most egg sacs contained over 70 eggs, each 0.7–1.0 mm in diameter. Embryos of both species were incubated at room temperature (22–24 °C), or at 18 °C to retard development.
Time-lapse imaging and tracing Embryos were immersed in mineral oil (Sigma) to clear the chorion. Time-lapse frames were captured every 3–5 min using Astro IIDC software running on Macintosh computers. Prisms were sometimes used to image the blastoporal region. Using Adobe Photoshop, all frames were cropped and adjusted for brightness and contrast; a high-pass sharpening filter was used to sharpen cell borders in some movies. Batch-processing was automated for consistency and convenience. Individual cells were traced by hand on individual frames.
CM-DiI injection CM-DiI (1,1′-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate) (Invitrogen) is a fixable DiI. It was diluted in 16 % DMSO in 80 % ethanol in PBS and used at 170 μg/mL. In L. mactans, 0.5 nL was injected, and in C. mildei, up to 2 nL was injected. Embryos were periodically photographed under white light and under 560 nm excitation.
Fixation C. mildei embryos at various stages were collected and treated with Ilsa (58 % methanol, 17 % chloroform, 17 % DMSO, 8 % acetic acid; made fresh, see ). Embryos were stepped into 100 % methanol, and stored at −20 °C. Embryos were postfixed by stepping into room temperature PBS, transferred into 4 % paraformaldehyde in PBS made fresh and manually demembranated using tungsten needles and watchmaker’s forceps. Demembranation was completed in 0.1 % Triton X-100 in PBS as necessary to ensure that total time in paraformaldehyde did not exceed 30 min.
Latrodectus mactans embryos were dechorionated using a 50 % percent bleach solution and fixed in Ilsa until opaque. Glass or tungsten needles and watchmaker’s forceps were used to remove the vitelline membranes in one of various postfixation formulas, see below.
For histology, postfixation was carried out in Nu–Nu Fix (4 % paraformaldehyde, 4 % glacial acetic acid, 1 mM each calcium chloride and magnesium sulfate in PBS) for 30–60 min. In some cases, the embryos were fixed for 48 h and then postfixed in 1 % paraformaldehyde in PBS for 5 days. For immunostaining, Nu–Nu Fix + 5 % DMSO was used for 15 min maximum. After postfixation, embryos were stepped into methanol for histology or storage at −20 °C, or were moved directly onto antibody staining.
Embedding and sectioning To aid in orientation, postfixed embryos were pre-stained with Eosin B-Phloxine (3 drops 0.1 % stock in 10 mL methanol) or Delafield’s hematoxylin in methanol in the same proportions. They were stepped into paraffin via graded series of methanol, tert-butyl alcohol, and mineral oil. Blocks were sectioned until tissue was encountered and soaked overnight in 5 % glycerol. Paraffin sections 6–8 μm were mounted with degassed Mayer’s albumen and stained with Delafield’s Hematoxylin and Eosin B-Phloxine; or Delafield’s Hematoxylin and Eosin B-Phloxine + 0.02 % Fast Green for L. mactans; or with Nuclear Fast Red + Orange G + 5 % Phosphotungstic acid + Black’s Aniline Blue Orange G (spiderlings). DAPI 1:1000 was used as a counterstain for some CM-DiI-injected specimens. Sections were coverslipped with Pro-Texx Mounting Medium (Baxter Diagnostics).
Antibody staining and confocal microscopy Embryos were stepped into PTD (0.1 % Triton + 5 % DMSO in PBS), washed 5X in PTD, blocked 30 min in 5 % normal goat serum + 5 % DMSO + 0.02 % sodium azide in PTD. Embryos were stained overnight at room temperature in 1:1000 mouse anti-tubulin (Sigma) in blocking solution and washed and blocked as above. Embryos were incubated overnight at room temperature in 1:1000 Alexa-conjugated goat anti-mouse (Invitrogen) in blocking solution and then washed again and stepped into methanol. To stain nuclei, embryos were incubated overnight at 4 °C in 1:1000 Yo-Pro-1 in methanol, washed 3 times in methanol, and cleared with methyl salicylate. Images were acquired with an Olympus Fluoview confocal microscope and stacks were compiled in Image J (NIH.gov).
Latrodectus mactans and L. geometricus
Timing of cumulus internalization and its fate
Histology confirms that the cumulus cells internalize before other cell types
Evidence for internalization at the germ disc rim
Round cells of intermediate size are visible in the deep layer of histological sections late in gastrulation (Fig. 5g, green arrowheads). In sections of P. tepidariorum, Montgomery  notes apparent cell internalization around the rim of the germ disc, and in L. mactans Rempel  notes a chain of deep-layer cells linked in series and connected to the superficial layer at the germ disc rim. Our sections show virtually the same static image as presented by Rempel (Fig. 5c cf. his Fig. 26), and is compatible with internalization at the rim of the germ disc, perhaps by involution. This is consistent with the expression of At-twist and fkh at the rim of P. tepidariorum [18, 32]. However, the problem shared by histology and static gene expression patterns is that such studies cannot reveal the origin of the cells; for example, in the case of At-twist and At-fkh, cells expressing these markers are found at the rim but may have originated at the central blastopore and simply migrated. In P. tepidariorum, this issue was ultimately addressed by following a labeled clone in timelapse video, to obtain direct evidence of internalization at the rim . In Latrodectus, we followed the movements of individual cells at the rim in video recordings.
Although the chained array of cells seen in sections was suggestive of involution, our videos show no mass movements or inrolling—internalizing cells left the surface only by ingression. This pattern of individual ingression is also seen in embryos of L. geometricus, with more cells internalizing at the rim than in L. mactans (Fig. 6). As with L. mactans, L. geometricus cells internalize at multiple positions around the rim of the germ disc. We did not see internalization of cells in the central germ disc at this stage in timelapse movies of either species, and neither did we see bottle cells in the central region at these later stages in our extensive histological series.
Central and ring blastospores are distinct sites of internalization
Fate of the cumulus
Once the cumulus has migrated to the edge of the germ disc or the equivalent position in C. mildei, its cells disperse as the dorsal field forms. Until the present study, only Holm  was successful in following the fate of cells beyond dorsal field formation by labeling cumulus cells in A. labyrinthica with carmine powder. Holm was able to find carmine particles in the opisthosoma, but presented only one case. We raised four injected C. mildei embryos to hatching, and all labeled cells were found in the opisthosoma, confirming Holm’s basic finding (Fig. 8c). Most labeled cells were in the dorsolateral region of the abdomen. A limitation of our study is that development in oil (necessary for the injections) interferes with chitinization and molting, and development arrests after hatching. Organogenesis is not complete at this stage, particularly in the opisthosoma; so there is no absolute certainty regarding the ultimate adult fate of the labeled cells. However, histological sections of uninjected controls, including second instar and adult, suggest that the dorso-lateral abdomen is composed largely of gut and gut diverticula (Additional file 9: Figure S4). Therefore, the labeled cells probably form some portion of the digestive mass. This is consistent with molecular data that cumulus cells express endodermal, but not mesodermal markers [17, 18]. It is also possible that the labeled cells are fated to form visceral mesoderm.
Evaluation of cell internalization traits across spider phylogeny
Ingression of single cells before blastopore forms
Cumulus forms before Primitive Plate
Internalization at germ disc rim or extra-blastoporal site
Late internalization at caudal structure
Pit present a
Pit present a
Pit present a
The early gastrulation pattern in C. salei (Ctenidae) appears to follow the canonical model, in that an early deep layer forms first (‘primary thickening’), from which the cumulus emerges , but is there bona fide internalization at the periphery? Does the cumulus in P. tepidariorum internalize separately from other deep layer cells? Applying our methods to these species would help evaluate our working model. Definitive evidence for late internalization at a caudal structure exists only for Z. x-notata, in which a large group of cells is internalized through a structure termed the ‘caudal bud’ . In A. labyrinthica, I. karschi and P. tepidariorum, a pit is present at the vertex of the expanding dorsal field [12, 13, 17]. The presence of a pit would seem to indicate internalization; however, there is no direct evidence for caudal internalization in these species.
How unusual is gastrulation at multiple times and positions in the embryo? We are perhaps used to thinking of a single blastoporal region that functions continuously in such model systems as the frog with its annular blastopore or the chick and mouse with a linear primitive streak. There are, however, many examples of embryos with temporally and spatially separate points of internalization. The primary mesenchyme cells of many sea urchins ingress singly or in small groups hours before internalization of the archenteron, and a secondary invagination of the stomodeum completes the through-gut (reviewed in ). The fruit fly internalizes its mesoderm by invagination of the ventral furrow long before the anterior and posterior midgut invaginations at opposite ends of the egg move prospective endoderm into the interior. This pattern of separated mesoderm and endoderm internalization holds for many other insects . Similarly, gastrulation in non-malacostracan crustaceans often involves internalization of mesoderm and endoderm separated in time, space, or both; and that of malacostracans also involves early ingression followed by mass internalization of mesendoderm . Thus, spatial and temporal separation of internalizing cell populations is not unusual, particularly in groups with relatively early specification of cell fate.
Observations of living embryos without experimental challenge cannot answer questions of cell fate determination. Nevertheless, we believe our results are consistent with the view that the cells of the cumulus are fated as such before their internalization. Timelapse videos show that the cumulus cells ingress first in all species we studied, including Z. x-notata , and the identity of these early ingressors is confirmed by CM-DiI injection in L. mactans and C. mildei: only cumulus mesenchyme cells are labeled by early injection into the deep layer. The cumulus cells, thus, exhibit a unique behavioral phenotype that correlates with a unique molecular phenotype (dpp expression in P. tepidariorum ). Both observations challenge the canonical view that the cumulus cells differentiate by cell–cell interaction within the deep layer. Our tracings and classic experiments by Holm suggest an endodermal fate for the cumulus , consistent with expression in central deep cells of forkhead , a marker of early endoderm in Drosophila. A more complete understanding of the state of determination of the cells of the early spider gastrula will require cell ablation and transplant studies.
This paper has emphasized the embryology of early spider development to reveal that the canonical model of spider gastrulation is not accurate for all species. Are the data potentially useful in understanding other aspects of spider biology? The variation in gastrulation strategies among the different species (summarized in Table 1) may be of value in clarifying phylogenetic relationships. The monophyly of the orb-weavers (Orbiculariae), which includes Z. x-notata (Araneidae) and the cobweb-weavers P. tepidariorum and Latrodectus spp. (Theridiidae), is methodologically disputed [39, 40]. The reason for this dispute is that the characters which establish the monophyly are almost entirely behavioral , while molecular data are conflicted [42, 43], but tend not to support monophyly of the Orbiculariae [44–46]. However, our data suggest that the Orbiculariae may be united by shared developmental similarities that vary from the canonical model, namely early cumulus ingression and late cell internalization at an extra-blastoporal site. The three spiders whose development seems most similar to the canonical model are all members of the RTA clade (a diverse Entelegyne lineage) [47, 48]: A. labyrinthica (Agelenidae), C. salei (Ctenidae), and C. mildei (Eutichuridae, assigned by ). Most phylogenies place the RTA clade as sister group to the Orbiculariae . Wolff and Hilbrant  report that gastrulation in C. salei largely follows the canonical model; however, we found notable variation from the model in C. mildei that could not be easily detected without tracing individual cells. Our data from C. mildei are the first evidence of multi-phase gastrulation outside the Orbiculariae. Evidence (or evidence of absence) for multi-phase gastrulation should be sought in the popular spider systems, C. salei and P. tepidariorum, and in the historical spider model, A. labyrinthica, to help clarify these evolutionary relationships.
Our cell tracings and those of [26, 29] show that gastrulation in spiders typically involves cell internalization at both a central blastopore and, at varying later times, internalization at an extra-blastoporal site. Internalization occurs at the peripheral rim of the germ disc in P. tepidariorum and Latrodectus spp.; at an annulus distinct from the central blastopore in C. mildei; and at the caudal bud in Z. x-notata. In contrast, there is presently no evidence for extra-blastoporal internalization in C. salei or the historical model A. labyrinthica, although the latter has not been studied with modern methods. Our working model shown in Figs. 2 and 9 reflects our view that multiple regions of cell internalization are typical for spiders.
Live-cell labeling with CM-DiI and cell tracings demonstrate that cells of the prospective cumulus (dorsal organizer) internalize first, well before general mesendoderm ingresses into the deep layer. Injection of CM-DiI into the deep layer beneath the central blastopore early in gastrulation labels only cumulus mesenchyme cells. We show that these cells’ daughters come to populate the deep endoderm of the opisthosoma, confirming Holm’s work in A. labyrinthica. After the cumulus has begun migration, CM-DiI injection into the same region labels non-cumulus mesoderm and endoderm. Although live labeling cannot definitively address the state of cell determination in any system, the early ingression of the prospective cumulus as a distinct event in gastrulation is consistent with early, cell-autonomous specification of this cell type. Cell–cell interaction within the deep layer of the primitive plate is unlikely to be required for formation of the cumulus, as the cumulus begins to migrate in many species before the deep layer contains many other cells. Our working model incorporates early internalization and cell-autonomous formation of the cumulus.
The demonstration of multiple sites of gastrulation in spiders accords with data from many other arthropod systems, from crustaceans to flies. Multiple gastrulation sites may not be universal among spiders, however, and a wider sampling of spider taxa may reveal systematic variation that could be useful in establishing phylogenetic relationships. Another character of possible utility is origin of the cumulus, which could form either by cell-autonomous mechanisms or by cell–cell interaction within an undifferentiated deep layer.
cumulus (dorsal organizer)
0.1 % Triton + 5 % DMSO in PBS
retrolateral tibial apophysis
SB conceived the study; AE, CB, and KL conducted experiments; all authors analyzed data, developed the conclusions, and participated in writing drafts of the manuscript; AE and SB wrote the final version. All authors read and approved the final manuscript.
This research was supported by Grants to SB from the M. J. Murdock Charitable Trust and the NIH (1R15HD064188-01). AE was supported by a Mellon grant to Reed College. We thank J Turner for sharing her detailed observations on L. mactans gastrulation; A Trail for filming L. geometricus; M Burrill for L. geometricus histology and the cover image of C. mildei; E Vance for sharing her original illustrations; C Kristensen for generously mating the widows and advice on husbandry; Dr. D Lyons for helpful comments on an earlier version of the text; and Dr. R Chaw and two anonymous reviewers for constructive criticism of the manuscript.
The authors declare that they have no competing interests.
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