The dermomyotome ventrolateral lip is essential for the hypaxial myotome formation
© Pu et al.; licensee BioMed Central Ltd. 2013
Received: 22 March 2013
Accepted: 11 October 2013
Published: 18 October 2013
The myotome is the primitive skeletal muscle that forms within the embryonic metameric body wall. It can be subdivided into an epaxial and hypaxial domain. It has been shown that the formation of the epaxial myotome requires the dorsomedial lip of the dermomyotome (DML). Although the ventrolateral lip (VLL) of the dermomyotome is believed to be required for the formation of the hypaxial myotome, experimentally evidence for this statement still needs to be provided. Provision of such data would enable the resolution of a debate regarding the formation of the hypaxial dermomyotome. Two mechanisms have been proposed for this tissue. The first proposes that the intermediate dermomyotome undergoes cellular expansion thereby pushing the ventral lateral lip in a lateral direction (translocation). In contrast, the alternative view holds that the ventral lateral lip grows laterally.
Using time lapse confocal microscopy, we observed that the GFP-labelled ventrolateral lip (VLL) of the dermomyotome grows rather than translocates in a lateral direction. The necessity of the VLL for lateral extension of the myotome was addressed by ablation studies. We found that the hypaxial myotome did not form after VLL ablation. In contrast, the removal of an intermediate portion of the dermomyotome had very little effect of the hypaxial myotome. These results demonstrate that the VLL is required for the formation of the hypaxial myotome.
Our study demonstrates that the dermomyotome ventrolateral lip is essential for the hypaxial myotome formation and supports the lip extension model. Therefore, despite being under independent signalling controls, both the dorsomedial and ventrolateral lip fulfil the same function, i.e. they extend into adjacent regions permitting the growth of the myotome.
KeywordsSomite Dermomyotome Myotome Chicken embryo
The musculature of the body consists of an epaxial and hypaxial component. The epaxial component is composed of the deep back muscles which originate solely from the myotome. In contrast, the hypaxial component includes muscles of the ventrolateral body wall, girdle, limb and tongue. The hypaxial portion yields muscle in different ways. Muscle cells of the limb and tongue muscles and the lateral shoulder girdle muscles are derived from the migrating myogenic precursor cells from the somite. In contrast, the ventrolateral body wall muscles (intercostal and abdominal muscles) and the medial shoulder girdle muscles are formed from the myotome [1–6]. A part of the shoulder girdle muscles, the trapezius and sternocleidomastoideus muscle, originate from the lateral plate mesoderm .
The myotome, is the primitive skeletal muscle that forms within embryonic metameric structures called the somite. The somite is initially an epithelial sphere, surrounding a mesenchymal core [8, 9]. The mature somite compartmentalizes into a dorsal and a ventral part. The ventral part undergoes an epithelial to mesenchymal transition to form the sclerotome which gives rise to axial cartilages, bones, and tendons [10–12]. The dorsal portion remains as an epithelium and forms a cell sheath, called the dermomyotome, which contributes to the formationof the dorsal dermis and skeletal muscle. The four margins of the dermomyotome fold ventrally and form lip-like borders, called the dorsomedial (DML), ventrolateral (VLL), cranial and caudal dermomyotomal lips. The dermomyotomal lips contribute to myogenic cells in two ways. To form the limb muscle, undifferentiated muscle precursor cells delaminate from the VLL and undergo a long distance migration into the limb bud, where they differentiate into muscle cells . To form the myotome, muscle precursor cells delaminate from all four lips and differentiate into mononuclear myocytes immediately under the dermomyotome [13, 14].
The myotome morphogenesis has been extensively studied using the avian model. In a descriptive study using immunohistochemistry staining of myotomal cells, Kaehn et al. suggested that the myotome forms in a medial-to-lateral direction . This model postulates that the oldest myotome cells should be located at the extreme medial margin of the myotome and the youngest at the lateral margin. Based upon fluorescent cell lineage-tracing analysis, however, Denetclaw et al. [16, 17] advocated an incremental growth model in which the myotome is predicted grow in the opposite direction. According to this model, new cells are added to the myotome in a lateral-to-medial order. Further observations made by this group showed a two phase model of the myotome formation [18, 19]. In the first phase, myocytes from the DML form a thin layer of myotome. In the second phase, new myocytes derived from all four lips are recruited in a superficial-to-deep direction. In contrast, studies using thymidine dating suggested an intercalating growth model for myotome morphogenesis [20–24]. According to this model developed by Kalcheim et al, the first myotomal cells form pioneer cells which serve as a scaffold for the secondary myotomal cells. The pioneer cells translocate first from the DML to the ventral position under the dermomyotome. They then migrate to the cranial border, where they elongate towards the caudal border. The myotome cells of the second wave migrate from both cranial and caudal lip into the myotome between the pioneer cells. Using live imaging, Gros and colleagues provide a comprehensive two step model of myotome formation . In the first step, the myotome is formed by an incremental growth. Cells translocate from the DML and elongate bidirectionally, towards to cranial and caudal border of the dermomyotome. In the second step, the myotome is formed by an intercalating growth. Cells from the cranial and caudal border enter the scaffold made by the first myotomal cells originated from the DML.
Though the myotome is made up of the similar mononuclear myoblast, its epaxial and hypaxial part originate from two different sources and develop through different mechanisms. Cell lineage tracing experiments in chick embryos performed by Denetclaw and Ordahl  and Gros et al.  showed that the epaxial myotome is derived from the medial half of the somite, while the hypaxial myotome arises from the lateral half of the somite. After ablation of the DML, the medial myotome was truncated. Furthermore, the myotome formation in a DML-ablated somite could be restored by transplantation of a second DML from a donor embryo. Cell lineage tracing revealed that new myotome cells are derived from the donor DML. Based upon these observations Ordahl et al.  conclude that the DML drives the dorsal-to-medial growth of the dermomyotome which is essential for the medial extension of the myotome. Eloy-Trinquet and Nicolas characterised the formation of the epaxial and hypaxial myotome and concluded that they originate from distinct cell population . The VLL has always been assumed to execute the same function as the DML during the hypaxial mytome morphogenesis. However, this view is not supported by experimentally evidence. In this study, we analysed the myotome formation after surgical ablation of the VLL in chick embryos. Our findings demonstrate that the VLL is required for the hypaxial myotome formation.
The dermomyotome ventrolateral lip grows into the somatopleura
Additional file 1: Live imaging of GFP labelled dermomyotomal ventrolateral lip.(WMV 9 MB)
Additional file 2: Live imaging of GFP labelled dermomyotomal ventrolateral lip.(WMV 1 MB)
Removal of the dermomyotome ventrolateral lip affects the ventrolateral growth of the dermomyotome and myotome
Cells of the intermediate part of the dermomyotome can not restore the ablated VLL
Embryos from the above manipulation were subsequently analysed for Pax3 expression. The Pax3-expression of the VLL of one embryo (n = 5/5) was missing with the exception of the cranial and caudal edge (Figure 2F). The Pax3-expression in the cranial and caudal part of the VLL could be explained due to the incomplete removal of the VLL. Accordingly, the most lateral part of the myotome viewed by the myosin heavy chain antibody (Mf20) was partly disturbed (data not shown).
Removal of the intermediate part of the dermomyotome epithelium does not significantly affect the myotome formation
Next we ask whether the intermediate part of the dermomyotome epithelium is essential for the growth of the hypaxial myotome. First we investigated the ventrolateral growth of VLL after ablations of the intermediate dermomyotome at the interlimb level. The VLL primordium of interlimb somites was labelled through GFP by electroporation at HH-16/17 as described above. Then, the intermediate part of a dermomyotome was removed. After one to two days of reincubation, the GFP-marked VLL of the operated somites extended as far as those of unoperated somites in all analyzed embryos (n = 8/8, Additional file 4: Figure S2). The VLL was completely normal. The Pax3-expression was only partly down-regulated in the intermediate part of the operated dermomyotome. The myotome in the operated somite showed no significant change comparing to the un-operated somites (Additional file 4: Figure S2).
In this study, we investigated the function of the dermomyotome ventrolateral lip (VLL) using surgical ablation technique in the chick embryo. A complication of this procedure is that it is difficult to remove all VLL cells and the remaining cells can reconstitute the ablated tissue. Therefore when small regions are ablated, the phenotype is limited due to regeneration. This can be circumvented by ablating the VLL from consecutive somites. This is a possible explanation why others who have carried out limited ablation experiment have failed to induce changes in myotome growth.
We never observed labelled intermediate dermomyotome moving to the position of the previously ablated VLL. Combined with the observation that the hypaxial myotome truncated after removal of the VLL of 3 somites, we can conclude that the function of the VLL can not be replaced by the intermediate dermomyotome. After removal of the intermediate part, the myotome formed almost normally. It is possible that the remaining cells of the intermediate part could compensate the lost cells, thereby generating enough myocytes for the myotome. These findings would suggest that the intermediate dermomyotome is not essential for the ventrolateral growth of the VLL. The time-lapse data showing the VLL growth supports this interpretation.
The somite contains at least two muscle lineages in its medial and lateral halves, which developmental cell fate is environment dependent [32, 33]. The myotomal myogenesis within the medial and lateral somite half occurs in a spatially and temporally different context. The development of the hypaxial myotome is delayed several stages compared to the epaxial myotome . The DML which has been shown to drive the growth and arrangement of the epaxial myotome is always in contact with the surface ectoderm and neural tube during the myotome growth . In contrast, the specification of the hypaxial dermomyotome is induced by lateralising signals from the lateral plate mesoderm/intermediate mesoderm and dorsalising signals from the surface ectoderm . At later stages, the VLL grows into the somatopleura and loses contact with the surface ectoderm. In fact, the VLL is very far away from the ectoderm. The signalling mechanisms controlling the epaxial and hypaxial myotome formation are also different. The medial somite receives signals emanating from the notochord (Shh, Noggin) as well as the neural tube and ectoderm (Wnts, BMPs). These signals coordinate the induction of the epaxial properties of dermomyotome [35–37]. While Wnt-11 and En1 are expressed in the epaxial dermomyotome, Sim1 is expressed in the hypaxial dermomyotome [34, 35, 38–40]. Though the inducing signal is different, our results show that the VLL is irreplaceable for the formation hypaxial myotome, like the DML .
Our study demonstrates that the dermomyotome ventrolateral lip is essential for the hypaxial myotome formation. Despite being under independent signalling controls, both the dorsomedial and ventrolateral lip fulfil the same function, i.e. they extend into adjacent regions permitting the growth of the myotome.
Fertile chick eggs were obtained from the Institute of Animal Science, University of Bonn. The embryos were incubated at 38°C in a humidified atmosphere and staged according to Hamburger and Hamilton (1951) . Ethical approval of the experiments was not needed since all embryos studied here were younger than 10 days.
Electroporation of a GFP-vector
The electroporation procedure was performed as described by Scaal et al.  and Dai et al. . Briefly, electroporations were carried out at the interlimb level of HH-16/17 embryos. GFP-expressing plasmid pCLGFPA was introduced to the lateral part of the epithelial somite.
Time-lapse imaging was performed approximately 24 h after electroporation with a confocal laser scanning microscope (CLSM, Zeiss LSM 510). Embryos were aseptically cut into 200 μm thick horizontal slices with a McIlwain tissue chopper. Slices were attached to collagen-coated (Sigma-Aldrich, C7661) glass coverslips (32mm, Kindler, Freiburg, Germany) fixed by a plasma clot (Sigma, P3266) coagulated with thrombin (Calbiochem, 605157). Tissue slice cultures were used to study cell migration utilizing a Rose-chamber under a Zeiss 10x lens (Plan-Neofluar, NA 0.3). To maintain the incubation settings at 37°C and 5% CO2 on the microscope stage, a CTI controller 3700 digital, O2 controller, 37-2 digital Tempcontrol, and heating insert P (Zeiss) were used. Additionally the immersion oil objective was heated with a Tempcontrolmini system (Zeiss). For time-lapse imaging of the epithelial somite slices were captured for 10-24 h at 10 min intervals.
Embryo microsurgery was performed as described in previous works with the modification noted below [44–46]. Ablations of the ventrolateral lip (VLL) and intermediate part of the dermomyotome epithelium were performed in similar fashion. For VLL ablations, the dermomyotome epithelium was incised craniocaudally and slightly medial to the VLL. Tissue fragments located laterally to the cut were subsequently removed by mouth aspiration using a glass micropipette. For intermediate part ablations, a second parallel cut was made lateral to the dorsomedial lip (DML). Then the tissue between two cuts was removed. The egg was sealed with tape and reincubated.
Operated embryos were fixed in 4% PFA. Whole mount in situ hybridization with Pax3 was performed as described by Nieto et al. . After photograph, embryos were sectioned (20 μm) using a cryostat microtome.
Operated embryos were fixed in Dent’s fixative and then immunohistochemistry stained with the myosin heavy chain monoclonal antibody Mf20 (Developmental Study Hybridoma Bank, Iowa) and GFP polyclonal antibody. Primary Mf20 and GFP antibody were detected with goat-anti-mouse Cy3 and goat-anti-rabbit Cy2, respectively. After photograph, embryos were transversely sectioned in 20 μm thickness using a cryostat microtome.
The dorsomedial lip of the dermopmyotome
The ventrolateral lip of the dermomyotome
Green fluorescent protein.
We thank Developmental Studies Hybridoma Bank, Iowa City, IA, USA for the Mf20-antibody. The technical support of Sandra Graefe and Anke Lodwig is gratefully acknowledged. This study was supported by the German research foundation grant (DFG, Hu729/10) and the BBSRC (BBH01022X) as well as FoRum F647-09 and FoRum F732N-2011.
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