Immunohistochemical exploration of differentiation and angiogenesis marker expression in umbilical cord structures
DOI:
https://doi.org/10.52692/1857-0011.2025.2-82.28Keywords:
AC133, CD105, CD34, mesenchymal cells, progenitor cells, VEGFR-2Abstract
Far from being a mere supportive tissue, Wharton’s jelly functions as a living mesenchymal niche, containing cells with stem-like properties, molecular signals for differentiation, and hints of a tissue dialogue that remains incompletely understood. The aim of this study was to perform an immunohistochemical characterization of CD105, CD34, VEGFR-2, and AC133 marker expression in Wharton’s jelly, in order to highlight the phenotypic diversity and biological potential of its cellular component. The study was conducted on 26 human umbilical cords. The samples were fixed in 10% buffered formalin, then processed using standard histological techniques and embedded in paraffin. Sections were stained with hematoxylin-eosin and immunohistochemically for the markers CD105, CD34, VEGFR-2, and AC133. Marker expression was evaluated semi-quantitatively in three regions of Wharton’s jelly, and the data were analyzed morphologically and statistically. CD105 showed strong expression, particularly in the peripheral zone of Wharton’s jelly, indicating the presence of a mesenchymal population with differentiation potential. CD34 and AC133 highlighted progenitor cell subpopulations with focal distribution and low to moderate intensity. VEGFR-2 was expressed in both endothelial and stromal cells, as well as in the extracellular matrix. A partial overlap of expression zones was observed for the studied markers, without complete cellular co-expression. The study revealed the active, heterogeneous, and functional nature of Wharton’s jelly, suggesting the existence of a complex cellular microenvironment capable of supporting processes such as cellular differentiation and angiogenesis.
References
Parolini O, Soncini M, Evangelista M, Schmidt D. Amniotic membrane and amniotic fluid-derived cells: potential tools for regenerative medicine? Regenerative Medicine. 2009;4(2):275–291.
Wang HS, Hung SC, Peng ST, et al. Mesenchymal stem cells in the Wharton’s jelly of the human umbilical cord. Stem Cells. 2004;22(7):1330–1337.
Troyer DL, Weiss ML. Wharton’s jelly-derived cells are a primitive stromal cell population. Stem Cells. 2008;26(3):591–599.
El Omar R, Beroud J, Stoltz JF, Menu P, Velot É, Decot V. Umbilical cord mesenchymal stem cells: the new gold standard for mesenchymal stem cell-based therapies? Tissue Eng Part B Rev. 2014;20(5):523– 544.
Barry FP, Murphy JM. Mesenchymal stem cells: clinical applications and biological characterization. The International Journal of Biochemistry & Cell Biology. 2004;36(4):568–584.
Fina L, Molgaard HV, Robertson D, et al. Expression of the CD34 gene in vascular endothelial cells. Blood. 1990;75(12):2417–2426.
Peichev M, Naiyer AJ, Pereira D, et al. Expression of VEGFR-2 and AC133 by circulating human CD34(+) cells identifies a population of functional endothelial precursors. Blood. 2000;95(3):952–958.
Bieback K, Kern S, Klüter H, Eichler H. Critical parameters for the isolation of mesenchymal stem cells from umbilical cord blood. Transfusion. 2004;44(5):642–648.
Mitchell KE, Weiss ML, Mitchell BM, et al. Matrix cells from Wharton’s jelly form neurons and glia. Stem Cells. 2003;21(1):50–60.
Baksh D, Yao R, Tuan RS. Comparison of proliferative and multilineage differentiation potential of human mesenchymal stem cells derived from umbilical cord and bone marrow. Stem Cells Dev. 2007;16(4):513– 522.
Sarugaser R, Lickorish D, Baksh D, Hosseini MM, Davies JE. Human umbilical cord perivascular cells (HUCPVCs) maintain multipotency and produce proangiogenic molecules. Stem Cells. 2005;23(9):1284–1294.
Harrell CR, Simovic Markovic B, Fellabaum C, Arsenijevic A, Volarevic V. Therapeutic potential of mesenchymal stem cell-derived exosomes in the treatment of eye diseases. Front Cell Dev Biol. 2019;7:85.
Kogler G, Sensken S, Airey JA, et al. A new human somatic stem cell from placental cord blood with intrinsic pluripotent differentiation potential. J Exp Med. 2004;200(2):123–135.
Bühring HJ, Treml S, Cerabona F, et al. Phenotypic characterization of distinct human bone marrow- derived mesenchymal stem cell subsets. Stem Cells Dev. 2007;16(5):887–896.
Fong CY, Chak LL, Biswas A, et al. Human Wharton’s jelly stem cells have unique transcriptome profiles compared to human embryonic stem cells and other mesenchymal stem cells. Stem Cell Rev Rep. 2010;6(3):385–393.
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