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  4. The Germinal Origin of Salivary and Lacrimal Glands and the Contributions of Neural Crest Cell-Derived Epithelium to Tissue Regeneration

The Germinal Origin of Salivary and Lacrimal Glands and the Contributions of Neural Crest Cell-Derived Epithelium to Tissue Regeneration

Int. J. Mol. Sci., 2023 · DOI: 10.3390/ijms241813692 · Published: September 5, 2023

Genetics

Simple Explanation

The study investigates the origin of salivary and lacrimal glands, which are exocrine glands in the head and neck. It uses transgenic TRiCK mice, which express fluorescent proteins under the control of genes that mark the neuroectoderm, mesoderm, and endoderm. The research demonstrates that these glands contain cells derived from all three germ layers. A subset of cells expressing Sox1, a marker for neuroectoderm, differentiated into epithelial cells, suggesting they are derived from neural crest cells. These cells also expressed stem cell markers and were prominent in tissue injury models, indicating their role in regenerative processes after tissue damage. The findings clarify the germinal origin of exocrine glands and highlight the contribution of neural crest-derived cells within the glandular epithelium to the regenerative response following tissue damage.

Study Duration
Not specified
Participants
TRiCK mice, Krt14-cre mice, C57BL/6 mice
Evidence Level
Not specified

Key Findings

  • 1
    Salivary and lacrimal glands contain cells derived from all three germ layers (ectoderm, mesoderm, and endoderm).
  • 2
    A subset of Sox1-driven fluorescent cells differentiated into epithelial cells, implying their neural crest origin and expression of stem cell markers.
  • 3
    Neural crest-derived epithelial cells are involved in regenerative processes following tissue injury in duct ligation and wound damage models.

Research Summary

This study investigates the germinal origin of salivary and lacrimal glands using transgenic TRiCK mice, revealing that these glands contain cells derived from all three germ layers: neuroectoderm, mesoderm, and endoderm. The research identifies a subset of Sox1-driven fluorescent cells that differentiate into epithelial cells, suggesting their neural crest origin. These cells also express high levels of stem cell markers and are particularly pronounced in duct ligation and wound damage models. The study concludes that neural crest-derived epithelial cells contribute to the regenerative response following tissue damage, providing evidence clarifying the germinal origin of exocrine glands.

Practical Implications

Understanding Gland Development

The study provides a deeper understanding of the complex developmental origins of salivary and lacrimal glands, revealing contributions from all three germ layers and neural crest cells.

Regenerative Medicine

The identification of neural crest-derived cells in tissue repair suggests a potential source for regenerative medicine approaches aimed at functional reconstruction of salivary and lacrimal glands.

Clinical Relevance

The findings could contribute to improved treatments for gland-related diseases and injuries, such as Sjögren's syndrome and salivary gland dysfunction.

Study Limitations

  • 1
    The identity of Sox17-dependent mCerulean-positive cells (putative endodermal cells) was not thoroughly investigated.
  • 2
    Variations were noted in the frequency of Venus-positive cell appearance in the epithelium of the mice used in this study, as well as in the appearance of neural crest-derived cells in SMG injury experiments.
  • 3
    The labeling of Sox1-dependent Venus-positive cells may not be complete due to insufficient Cre recombination.

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