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Precursor and interstitial Cajal cells in the human embryo liver
Mugurel Constantin Rusu1, Irina Dută, Andreea Cristiana Didilescu
1Discipline of Anatomy, Faculty of Dental Medicine, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania; anatomon@gmail.com.
Interstitial Cajal Cells (ICCs) and telocytes (TCs) were identified in human embryonic liver (HEL) tissue. These cells, expressing DOG1, suggest a role in early liver development and warrant further investigation in fetal liver research.
Area of Science:
- Developmental biology
- Hepatology
- Cell biology
Background:
- Interstitial Cajal Cells (ICCs) presence is established in adult human liver, but their immunophenotypes in the human embryonic liver (HEL) are poorly understood.
- A hypothesis suggests ICCs exist in HEL and are distinct from precursor/progenitor cell populations.
Purpose of the Study:
- To investigate the presence and immunophenotypes of cell types, including potential ICCs, in the human embryonic liver.
- To characterize cell populations in the HEL using specific antibody markers.
Main Methods:
- A qualitative study was conducted on five human embryos (23-29 mm).
- Immunohistochemistry was performed using antibodies against CD117/c-kit, CD31, CD34, CD90, CD105, DOG1, Ki67, and adiponectin.
Main Results:
- Blasts and hematopoietic cells were the predominant cell types.
- Interstitial cells with characteristic morphology were found, expressing DOG1 and sparsely CD117/c-kit, leading to their identification as ICCs or telocytes (TCs).
- Blasts were generally CD34-/CD105+, with some CD117/c-kit+ and CD90+ cells. Hematopoietic precursors were Ki67+, and adiponectin was found on blast plasmalemmas. Endothelia were CD31+/CD34+.
Conclusions:
- The study identified Interstitial Cajal Cells (ICCs) and/or telocytes (TCs) in the human embryonic liver, characterized by DOG1 expression.
- Further research is needed to correlate precursor cell types and immunophenotypes during human liver organogenesis.
- Investigation of ICCs/TCs in the human fetal liver is recommended.
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