The Ultrastructure of Hepatic Stellate Cell-Macrophage Intercellular Crosstalk as a New Morphological Insight into Phenomenon of Fibrogenesis in Pediatric Autoimmune Hepatitis

• Published in: Journal of clinical medicine Vol. 12; no. 3; p. 1024
• Main Authors: Łotowska, Joanna Maria, Sobaniec-Łotowska, Maria Elżbieta, Bobrus-Chociej, Anna, Sobaniec, Piotr
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 28-01-2023; MDPI
• Subjects: Biopsy; Clinical medicine; Extracellular matrix; Hepatitis; Hepatology; Histopathology; Immunology; Laboratories; Liver cirrhosis; Liver diseases; Medical research; Microscopy; Morphology; Patients; Pediatrics; Serology; Smooth muscle; transitional hepatic stellate cells (T-HSCs); activated Kupffer cells/macrophages (KCs/MPs); hepatic stellate cell (HSC) population; nonparenchymal hepatic cells (NPCs); liver fibrogenesis; ultrastructural studies; pHSCs; pediatric autoimmune hepatitis (AIH); cellular crosstalk; iHSCs
• ISSN: 2077-0383; 2077-0383
• DOI: 10.3390/jcm12031024

The aim of the study was the pioneering retrospective ultrastructural evaluation of respective forms of hepatic stellate cells (HSCs) and analysis of their crosstalk with other adjacent nonparenchymal cells (NPCs), especially Kupffer cells/macrophages (KCs/MPs), in pediatric autoimmune hepatitis (AIH).
Ultrastructural assessment of the HSC population and NPCs was performed in transmission electron microscopy (TEM) using pretreatment liver biopsies from 25 children (8 boys and 17 girls) aged 4-17 with clinic-pathologically diagnosed untreated AIH.
Submicroscopic evaluation allowed easy identification of numerous HSCs in the form of transitory cells, i.e., T-HSCs, accompanied by signs of fibrosis. T-HSCs included cells with features of activation initiation (iHSCs) and activation perpetuation (pHSCs), indicating high HSC activation plasticity. The pHSCs were markedly elongated and mainly showed a distinct loss of lipid cytoplasmic material, expanded and dilated channels of granular endoplasmic reticulum, and linear bundles of microfilaments beneath the cell membrane. They were surrounded by usually mature collagen fibers. Frequently activated KCs/MPs adhered directly to T-HSCs. Between them, tight intercellular junctions were formed by means of point desmosomes.
Our qualitative TEM observations indicate a key role of T-HSCs in liver fibrogenesis in pediatric AIH, with the essential involvement of activated KCs/MPs that directly adhere to them. Tight intercellular junctions, being the ultrastructural exponent of the specific cellular mechanisms of the crosstalk between NPCs, can play a vital role in hepatic collagen fibroplasia. A better understanding of HSC population morphology at the ultrastructural level in AIH seems important not only to improve the disease morphological diagnostics but to also provide new insights into therapeutic interventions for the phenomenon of liver fibrogenesis.