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Immunohistochemical-properties of the Dermal Embryonic Telocytes

Overview
Journal Sci Rep
Specialty Science
Date 2024 Jun 17
PMID 38886354
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Abstract

The current investigation aims to study the embryonic dermis formed in the early stages of development and identify the initial interstitial components of the dermis that serve as biological and structural scaffolds for the development of the dermal tissue. To investigate the dermal structure, the current study used morphological and immunological techniques. TCs identified by TEM. They had a cell body and unique podomeres and podoms. They formed a 3D network spread throughout the dermis. Homocellular contact established between them, as well as heterocellular contacts with other cells. Immunohistochemical techniques using specific markers for TCss CD34, CD117, and VEGF confirmed TC identification. TCs represent the major interstitial component in the dermal tissue. They established a 3D network, enclosing other cells and structures. Expression of VEGF by TC promotes angiogenesis. TCs establish cellular contact with sprouting endothelial cells. At the site of cell junction with TCs, cytoskeletal filaments identified and observed to form the pseudopodium core that projects from endothelial cells. TCs had proteolytic properties that expressed MMP-9, CD68, and CD21. Proteolytic activity aids in the removal of components of the extracellular matrix and the phagocytosis of degraded remnants to create spaces to facilitate the development of new dermal structures. In conclusion, TCs organized the scaffold for the development of future dermal structures, including fibrous components and skin appendages. Studying dermal TCs would be interested in the possibility of developing therapeutic strategies for treating different skin disorders and diseases.

References
1.
Sun C, Tian X, Jia Y, Yang M, Li Y, Fernig D . Functions of exogenous FGF signals in regulation of fibroblast to myofibroblast differentiation and extracellular matrix protein expression. Open Biol. 2022; 12(9):210356. PMC: 9471990. DOI: 10.1098/rsob.210356. View

2.
Zheng Y, Zhang M, Qian M, Wang L, Cismasiu V, Bai C . Genetic comparison of mouse lung telocytes with mesenchymal stem cells and fibroblasts. J Cell Mol Med. 2013; 17(4):567-77. PMC: 3822657. DOI: 10.1111/jcmm.12052. View

3.
Abd-Elhafeez H, Abou-Elhamd A, Soliman S . Morphological and immunohistochemical phenotype of TCs in the intestinal bulb of Grass carp and their potential role in intestinal immunity. Sci Rep. 2020; 10(1):14039. PMC: 7441181. DOI: 10.1038/s41598-020-70032-y. View

4.
Kalucka J, Bierhansl L, Wielockx B, Carmeliet P, Eelen G . Interaction of endothelial cells with macrophages-linking molecular and metabolic signaling. Pflugers Arch. 2017; 469(3-4):473-483. DOI: 10.1007/s00424-017-1946-6. View

5.
Massoud D, Abd-Elhafeez H, Emeish W, Fouda M, Shaldoum F, Alrashdi B . A transmission electron microscopy investigation suggests that telocytes, skeletal muscles, myoblasts, and stem cells in common carp (Cyprinus carpio) respond to salinity challenges. BMC Vet Res. 2024; 20(1):73. PMC: 10893627. DOI: 10.1186/s12917-024-03916-0. View