Heterogeneity of mesenchymal cells in human amniotic membrane at term

• Salvador Cortes-Sandoval ^[1] ; Vicente Seco-Rovira ^[2] ; Ester Beltrán-Frutos ^[2] ; María I. Serrano-Sánchez ^[2] ; Jesús Martínez-Hernández ^[2] ; Concepción Ferrer ^[2] ; Juan L. Delgado ^[2] ; Carmen L. Insausti ^[1] ; Miguel Blanquer ^[1] ; Luis M. Pastor ^[2]
  1. [1] Virgen de la Arrixaca University Hospital, IMIB, Murcia, Spain
  2. [2] School of Medicine, Regional Campus of International Excellence “Campus Mare Nostrum”, University of Murcia,Spain
• Localización: Histology and histopathology: cellular and molecular biology, ISSN-e 1699-5848, ISSN 0213-3911, Vol. 39, Nº. 5, 2024, págs. 573-593
• Idioma: inglés
• Enlaces
  • Texto completo
• Resumen

  • There is increasing interest in understanding the tissue biology of human amniotic membrane (hAM) given its applications in medicine. One cellular component is mesenchymal cells, which can be extracted, cultured and differentiated "in vitro" into various cell types. These studies show that there is heterogeneity among mesenchymal cells. The aim of this work is to study the membrane "in situ" to determine whether this cellular heterogeneity exists. The hAMs were obtained from caesarean deliveries at term and analyzed by histological techniques. Types I-III mesenchymal cells and Hofbauer were distinguished by light microscopy. Histochemically, mesenchymal cell types showed successively increasing positivity to: PAS, vimentin, fibronectin, and Concanavalin-A; VGEF, TGF-β2, PDGF-C, FGF-2. By the semiquantitative point of view, the percentage of Type II cells was 60%, significantly higher than the other types. With transmission electron microscopy, an intermediate cell type between II-III was observed. Strong vesiculation of the rough endoplasmic reticulum (RER) with exocytosis was observed. In addition, an accumulation of a similar material to the extracellular matrix in the RER caused its dilation especially in type IIITEM cells. Some of this material acquired a globular structure. These structures were also found free in the extracellular matrix. In conclusion, the mesenchymal cells of the fibroblastic layer of the hAMs studied are heterogeneous, with some undifferentiated and others with a probably senescent fibroblastic phenotype with accumulation in their RER of fibronectin. These results may be of interest to extract mesenchymal cells from hAMs for use in regenerative medicine and to better understand the mechanisms of fetal membrane rupture.