A Cranial Mesoderm Origin for Esophagus Striated Muscles.

Dev Cell

Department of Developmental & Stem Cell Biology, Institut Pasteur, Stem Cells & Development, CNRS URA 2578, 25 Rue du Dr. Roux, 75015 Paris, France. Electronic address:

Published: September 2015

AI Article Synopsis

  • - The esophagus connects the mouth to the stomach and helps in moving food by using muscles that are genetically traced to originate from the head rather than from the body's spinal structure (somites).
  • - Key genes Tbx1 and Isl1 are crucial for the development of esophagus striated muscles (ESMs), which are identified as a unique part of the cardiac and head muscle lineage in mice, differing from chick esophagus development.
  • - Unlike other muscle types, ESMs develop directly from fetal myofibers, utilizing smooth muscle as a support structure, which provides insights into conditions like esophageal disorders and congenital issues like DiGeorge syndrome.

Article Abstract

The esophagus links the oral cavity to the stomach and facilitates the transfer of bolus. Using genetic tracing and mouse mutants, we demonstrate that esophagus striated muscles (ESMs) are not derived from somites but are of cranial origin. Tbx1 and Isl1 act as key regulators of ESMs, which we now identify as a third derivative of cardiopharyngeal mesoderm that contributes to second heart field derivatives and head muscles. Isl1-derived ESM progenitors colonize the mouse esophagus in an anterior-posterior direction but are absent in the developing chick esophagus, thus providing evolutionary insight into the lack of ESMs in avians. Strikingly, different from other myogenic regions, in which embryonic myogenesis establishes a scaffold for fetal fiber formation, ESMs are established directly by fetal myofibers. We propose that ESM progenitors use smooth muscle as a scaffold, thereby bypassing the embryonic program. These findings have important implications in understanding esophageal dysfunctions, including dysphagia, and congenital disorders, such as DiGeorge syndrome.

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http://dx.doi.org/10.1016/j.devcel.2015.07.003DOI Listing

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