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Updated: Apr 3, 2026

Isolation of Myofibroblasts from Mouse and Human Esophagus
Published on: January 18, 2015
A Cranial Mesoderm Origin for Esophagus Striated Muscles
Swetha Gopalakrishnan1, Glenda Comai1, Ramkumar Sambasivan2
1Department of Developmental & Stem Cell Biology, Institut Pasteur, Stem Cells & Development, CNRS URA 2578, 25 Rue du Dr. Roux, 75015 Paris, France.
Esophagus striated muscles (ESMs) originate from cranial mesoderm, not somites, with Tbx1 and Isl1 as key regulators. These muscles develop uniquely, bypassing embryonic programs for direct fetal myofiber formation.
Area of Science:
- Developmental biology
- Muscle development
- Evolutionary biology
Background:
- The esophagus facilitates bolus transfer from the oral cavity to the stomach.
- The origin and developmental mechanisms of esophagus striated muscles (ESMs) remain incompletely understood.
- Previous research has not fully elucidated the embryonic origins or unique developmental pathways of ESMs.
Purpose of the Study:
- To determine the embryonic origin of esophagus striated muscles (ESMs).
- To identify key genetic regulators involved in ESM development.
- To investigate the evolutionary conservation and developmental strategy of ESMs.
Main Methods:
- Genetic tracing in mouse models.
- Analysis of mouse mutants for Tbx1 and Isl1.
- Comparative developmental studies using chick embryos.
Main Results:
- Esophagus striated muscles (ESMs) are derived from cranial mesoderm, not somites.
- Tbx1 and Isl1 are identified as crucial regulators for ESM development.
- ESM progenitors migrate anterior-posteriorly in mice but are absent in chicks, indicating evolutionary divergence.
- ESMs develop directly from fetal myofibers, utilizing smooth muscle as a scaffold, unlike other myogenic regions.
Conclusions:
- ESMs represent a third derivative of cardiopharyngeal mesoderm, alongside second heart field and head muscles.
- The unique developmental program of ESMs bypasses embryonic myogenesis.
- Findings offer insights into esophageal dysfunctions like dysphagia and congenital disorders such as DiGeorge syndrome.
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