A Region and Pathway Found Crucial for Facial Development in Vertebrate Embryos

Released: 17-Jul-2014 10:00 AM EDT
Embargo expired: 17-Jul-2014 12:00 PM EDT
Source Newsroom: Whitehead Institute for Biomedical Research
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Citations Cell Reports, July 17, 2014; 1R01 DE021109-01; F30DE022989

Newswise — CAMBRIDGE, Mass. (July 17, 2014) – A signaling pathway once thought to have little if any role during embryogenesis is a key player in the formation of the front-most portion of developing vertebrate embryos. Moreover, signals emanating from this region—referred to as the “extreme anterior domain” (EAD)—orchestrate the complex choreography that gives rise to proper facial structure.

The surprising findings, reported by Whitehead Institute scientists this week in the journal Cell Reports, shed new light on a key process of vertebrate embryonic development.

“The results are exciting on a number of levels,” says Whitehead Member Hazel Sive. “We uncovered two new and important things about facial formation, and it turns out they tie together.”

Sive and her lab have long been using the frog Xenopus as a model in which to study development of the EAD into the mouth. Several years ago, Amanda Dickinson, a postdoctoral researcher at the time, and Sive showed that the Wnt signaling pathway, which is active throughout the body in a wide array of developmental processes and in cancer, is vital for mouth formation. At the time, they observed that frog embryos whose Wnt signaling was disrupted only in the EAD not only failed to develop mouths, but also experienced other facial abnormalities. This suggested that the EAD may act on adjacent regions as a craniofacial “organizer” or signaling center.

Intrigued by this possibility, the lab searched for regulatory factors in the EAD that could affect craniofacial formation as a whole. Microarray analysis pointed to three highly expressed genes that also happen to be active participants in the Kinin-Kallikrein signaling pathway, best known in humans for its roles in regulating blood pressure, inflammation, and kidney function.

“We had no inkling that this pathway was active in the embryo,” says Sive.

The lab confirmed its findings through a series of loss-of-function (LOF) experiments in which they knocked out the expression of each of the three genes in developing embryos and observed the effects. In all cases, the facial regions displayed significant defects, ranging from a lack of a mouth opening to the absence of nostrils to abnormally small eyes. In addition, the migration of the neural crest, whose cells give rise to the nerves, cartilage, bones, and other components of the face, failed to occur normally.

Because the expression of two of the pathway genes yields the peptide Bradykinin, the researchers theorized that introducing Bradykinin into LOF embryos at the appropriate stage would allow them to develop normally. They implanted tiny beads soaked with Bradykinin peptides, rescuing not only mouth formation but also proper neural crest development. The Kinin-Kallikrein pathway ultimately produces the signaling molecule nitric oxide (NO). Not surprisingly, the scientists found reduced NO levels in their LOF embryos. As they predicted, peptide-soaked beads led to an increase in NO production, further confirming the role of the pathway and its genes during facial formation. Importantly, NO had not been thought critical for development of this region.

Finally, in an effort to determine whether the requirement for Kinin-Kallikrein signaling in craniofacial development is conserved, Sive lab graduate student Justin Chen turned to LOF experiments in zebrafish. They found one of the pathway genes to be necessary for proper formation of both the mouth and the neural crest.

“This study greatly enhances our overall view of craniofacial development,” says Laura Jacox, a graduate student pursuing a dual DMD-PhD degree through the Harvard School of Dental Medicine and the Harvard-MIT Health Sciences and Technology program. “Knowing what tissues are communicating with each other may help us determine where we could intervene to prevent or treat developmental abnormalities of the face.”

Jacox is co-first author of the Cell Reports paper along with postdoctoral researcher Radek Sindelka, who now heads a research group in Prague, Czech Republic.

It is unclear whether similar mechanisms are at play in mammals, including humans. Sive, however, hints that there may be a connection. She notes that certain blood pressure medications, which act on parts of the Kinin-Kallikrein pathway, can cause severe craniofacial defects in newborns if taken during pregnancy. Although such defects have been attributed to effects mediated by the kidneys, Sive’s latest findings may implicate Kinin-Kallikrein signaling.

This work is supported by the National Institute of Dental and Craniofacial Research (grants (1R01 DE021109-01 and F30DE022989) Harvard University’s Herschel Smith Graduate Fellowship.

Written by Matt Fearer

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Hazel Sive’s primary affiliation is with Whitehead Institute for Biomedical Research, where her laboratory is located and all her research is conducted. She is also a professor of biology at Massachusetts Institute of Technology.

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Full Citation:

“The Extreme Anterior Domain Is an Essential Craniofacial Organizer Acting through Kinin-Kallikrein Signaling”

Cell Reports, July 17, 2014

Laura Jacox (1,2,3,4,5), Radek Sindelka (1,6), Justin Chen (1,2) Alyssa Rothman (1), Amanda Dickinson (1,7) Hazel Sive (1,2)

1. Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
2. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
3. Harvard School of Dental Medicine, 188 Longwood Ave, Boston, MA 02115 USA.
4. Harvard Medical School, 250 Longwood Ave, Boston, MA 02115 USA. 5. Harvard Graduate School of Arts and Sciences, 1350 Massachusetts Avenue, Holyoke Center 350, Cambridge, MA 02138 USA.
6. Present address: Institute of Biotechnology, Videnska 1083, Prague 4, 14220, Czech Republic.
7. Present address: Virginia Commonwealth University, 1111 W Broad St, Richmond, VA 23220 USA.


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