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First published online 13 August 2003
doi: 10.1242/dev.00694


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Distinct modes of floor plate induction in the chick embryo

Iain Patten1,*, Paul Kulesa2,{dagger}, Michael M. Shen3, Scott Fraser2 and Marysia Placzek1,{ddagger}

1 Centre for Developmental Genetics, Department of Biomedical Science, University of Sheffield, Sheffield S10 2TN, UK
2 Beckman Institute 139-74, California Institute of Technology, Pasadena, CA 91125, USA
3 Center for Advanced Biotechnology and Medicine, UMDNJ-Robert Wood Johnson Medical School, 679 Hoes Lane, Piscataway, NJ 08854, USA



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Fig. 1. `Area a' cells populate the medial ventral midline. (A) Schematic of a HH stage 4 embryo, showing injection sites (asterisks) into `area a' and a more anterior reference site. (B) High-magnification images of DiI-labelled cells taken after 8 hours 20 minutes. Midline cells extend long, polarised cell processes, in excess of 100 µm in length (arrowhead) as they colonise the ventral midline. Arrow indicates DiI-labelled cells that have migrated anteriorly. (C-J) Still images from time-lapse, confocal analysis. Each image represents a single confocal section of DiI-labelled cells (arrowhead in C shows migrating cells; arrows in C-J show laterally moving cells migrating back into midline). `Area a' and anterior injection sites are indicated by red and yellow arrowheads, respectively (0 hours). The axis of the embryo is orientated such that the primitive streak lies towards the bottom right-hand corner of each panel. (K,L) Transverse sections of an `area-a'-injected embryo, analysed at HH stage 8. DiI labelling (red) is detected in ventral midline cells of the midbrain (K) and hindbrain (L). (M) Immunolabelling of the section shown in L with anti-Shh antibody (green) reveals that DiI-labelled cells populate the medial-most part of the ventral midline. Broken lines indicate outline of Shh-expressing floor plate, as determined by analyses such as shown in M.

 


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Fig. 2. `Area a'- and Hensen's node-derived cells do not intermingle during gastrulation. (A) Schematic of a HH stage 4 embryo, showing injection sites (asterisks) into `area a' (red) and Hensen's node (blue). Broken white arrow indicates the movement of Hensen's node cells into the deep mesodermal layer during axial mesoderm formation. (B-H) Still images from in vivo, time-lapse, confocal analysis of cell movements from `area a' (red, DiI-labelled cells) and Hensen's node (blue, DiD-labelled cells) during ventral midline formation. All images are single confocal sections, orientated with anterior towards the left and posterior towards the right. (Insets) Embryonic stage of development after 15 minutes (HH st4+), 75 minutes (HH st5) and 180 minutes (HH stage 6). (I) Transverse section through a HH stage 6 embryo, after labelling Hensen's node epiblast cells at HH stage 4. DiI-filled cells label the notochord exclusively (red; blue shows DAPI labelling). (Inset) Transverse section through a HH stage 8 embryo, after labelling Hensen's node epiblast cells at HH stage 4. DiI-filled cells label notochord and floor plate. Scale bars: 133 µm in C,D; 200 µm in B,E-H.

 


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Fig. 3. Specification of `area a' cells occurs after HH stage 4. (A) Left-hand panel: schematic of HH stage 4 embryo, showing `area a' (red) and Hensen's node (blue). Box indicates `area a' dissection. Right hand panel: whole-mount HH stage 4 embryo, showing Shh expression within Hensen's node (HN, white arrowhead) and anterior primitive streak. (B-E) Whole-mount views of HH stage 4 `area a' explants cultured for 40 hours and analysed for Shh, Hnf3b/Foxa2, Netrin1 and Sox2 expression. No expression of floor-plate markers is detected (B-D), but Sox2 expression (E) reveals that `area a' cells are specified as neural. (F-K) Midline neural explants isolated anterior to Hensen's node, in the region equivalent to `area a' and cultured in isolation for 24 hours. Explants taken from embryos at HH stage 4+ (F,G), HH stage 5 (H,I) and HH stage 6 (J,K) were processed for immunohistochemistry to determine expression of the floor-plate markers HNF3ß (F,H,J) and Shh (G,I,K). All panels show representative images of the results obtained and for each stage analysed show serial adjacent sections.

 


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Fig. 4. Prechordal mesoderm induction of early-forming floor-plate cells. (A) Expression of Gsc in a HH stage 4 embryo. Gsc-expressing cells are ablated in B. (B) HH stage 4 embryo, after removal of both endoderm and prechordal mesoderm. `Area a' cells remain intact, and are not deleted (white arrowhead). Black arrow indicates Hensen's node. (C) HH stage 4+ embryo, prepared for New culture. Removal of endoderm reveals that prechordal mesendoderm has begun to extend from the Node (white arrowhead). Black arrow points to Hensen's node. (D,G) Whole-mount view (D) and transverse section (G) of an 18 hour New cultured embryo, processed for Shh expression after prechordal mesoderm ablation at HH stage 4. Development is retarded, compared with control embryos (E,H), reaching HH stage 7. No expression of Shh can be detected on wholemounts (D). Sections reveal that the two halves of the neural plate are conjoined, although by only a few cells (black arrow in G) and that Shh cannot be detected in ventral midline cells (black arrow). Axial mesoderm cells are absent (white arrowhead, G). (E,H) Whole-mount view (E) and transverse section (H) of control embryos, processed for Shh expression. Expression of Shh is detected in both floor plate cells and axial mesoderm cells. (F,I) Whole-mount view (F) and transverse section (I) of an 18 hour New cultured embryo, processed for Shh expression after prechordal mesoderm ablation at HH stage 4+. Very weak expression of Shh is observed in the midline of operated embryos compared with controls, with fewer cells expressing Shh (white arrowhead in I; compare with H).

 


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Fig. 5. Early floor-plate cells differentiate in the absence of notochord. (A,C) Phase-contrast micrograph (A) and schematic (C) of HH stage 5 embryo, prepared for New culture, showing Hensen's node (HN, white arrowhead), notochord (nc, black bracket) and prechordal mesoderm (pm, black arrowhead). (B) Phase-contrast micrograph of same embryo, after removal of notochord. Hensen's node and prechordal mesoderm remain intact (white and black arrowheads, respectively). (D) Same embryo, 6 hours after notochord removal. A small rod of notochord cells emerge from Hensen's node (black arrow), but do not extend along the majority of the axis. A visible gap is observed under most of the neuraxis (black arrowhead). (E) Same embryo, analysed 24 hours post-operatively. Analysis of Shh expression reveals normal expression throughout the axis. (F-H) Transverse sections taken through levels depicted in E. A normal complement of floor-plate cells differentiates throughout the neuraxis, expressing normal, high levels of Shh. In the diencephalon, prechordal mesoderm cells expressing Shh can be detected (arrowhead in F). Notochord cells are absent in anterior regions of the axis, extending from the midbrain into the hindbrain (see transverse section, G). Notochord cells reappear in the anterior spinal cord (H).

 


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Fig. 6. HH stage 4+ prechordal mesendoderm is a potent inducer of floor-plate character in vivo. (A) Schematic, showing in vitro recombination experiments to determine the ability of HH stage 4+ prechordal mesoderm to induce floor-plate character. (B) Recombinate of HH stage 4+ chick prechordal mesoderm (Cpm) and E9.5 rat intermediate neural plate (np). After 48 hours in culture, rat neural plate expresses the floor-plate marker FP3, as assessed by immunohistochemistry. (C,D) Recombinate of HH stage 4+ quail prechordal mesoderm (Qpm) and HH stage 4 chick `area a'. After 24 hours in culture the position of the prechordal mesoderm was analysed by immunohistochemistry with an antibody against the quail specific nuclear marker QCPN (C, prechordal mesoderm delineated by broken lines). Analysis of HNF3ß expression by immunohistochemistry in an adjacent section reveals induction of floor plate cells in `area a' tissue that immediately abuts a small region of prechordal mesoderm (D). (E) Schematic and whole-mount views (inset) of in vivo grafts of mesodermal tissue. Grafts were inserted between the neural plate and the adjacent pre-somitic mesoderm in the posterior neuropore region of HH stage 10 embryos. (F) Control embryo. HNF3ß expression is restricted to the floor-plate region lying at the ventral midline of the neural tube. (G) Graft of a notochord next to the lateral wall of the neural tube (white asterisk in G) induces an ectopic floor plate as indicated by the localised expression of HNF3ß directly adjacent to the graft. (H) Graft of a HH stage 4+ prechordal mesendoderm (white asterisk) induces floor-plate character throughout the ipsilateral neural tube and also on the contralateral side of the neural tube (white arrowhead in H).

 


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Fig. 7. Induction of floor-plate character in `area a' cells through a cooperation between Shh and Nodal signalling. (A-F) Shh and Nodal are co-expressed in the HH stage 4+ prechordal mesoderm as it migrates underneath `area a'. Sections of HH stage 4 (A,B), 4+ (C,D) and 5 (E,F) embryos processed for mRNA in situ hybridisation with probes against Shh (A,C,E) or the chick Nodal gene Nr1 (B,D,E). The axial level of the sections, just anterior to Hensen's node, is indicated in the schematics to the left of each pair of images. At HH stage 4, no expression of either Shh (A) or Nodal (B) is observed in `area a' or the underlying tissue. Approximately 1 hour later, at HH stage 4+, Shh (C) and Nodal (D) are co-expressed in the nascent prechordal mesoderm lying underneath `area a' (white arrowheads in C and D). At HH stage 5, after the nascent prechordal mesoderm has passed underneath `area a', no expression of either Shh or Nodal is seen in the axial mesoderm (white arrowheads in E,F) while `area a'-derived cells of the neural midline now exhibit strong expression of Shh (black arrowhead in E). (G-Z) Nodal potentiates Shh signalling to induce floor plate character in `area a' explants in vitro. (G,L,Q,V) Exposure to 2 nM Shh induces expression of Shh, Netrin1 and HNF3ß in `area a' explants. (H,M,R,W) Exposure to 0.2 nM Shh is insufficient to induce floor-plate markers. (I,N,S,X) Exposure to Nodal alone can result in a very weak induction of ventral midline markers (I,N and inset in S), although sometimes elicits no ventral midline differentiation (S,X). (J,O,T,Y) Exposure of explants to a combination of 0.2 nM Shh and Nodal results in strong induction of ventral midline markers. (K,P,U,Z) Control medium does not elicit ventral midline differentiation.

 


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Fig. 8. Dual mode of floor-plate formation along the AP axis. (A) In the gastrulating chick embryo at HH stage 4+, prechordal mesoderm cells pass beneath `area a', and mediate a potent induction of `area a' cells to a floor-plate fate. (B) Once prechordal mesoderm cells have activated `area a' cells, they migrate further forwards, but are not required for any further induction of floor-plate character. Floor-plate cells that have been induced in `area a' migrate anteriorly and posteriorly. (C) In more posterior regions of the neuraxis, floor-plate cells require a prolonged period of contact with underlying notochord cells for their induction to a floor-plate fate.

 





© The Company of Biologists Ltd 2003