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Coxsackievirus and Adenovirus Receptor (CAR) Expression in Autopsy Tissues: Organ-Specific Patterns and Clinical Significance.
Ramamoorthy, Sudhakar; Garg, Sumit; Mishra, Baijayantimala; Radotra, Bishan Dass; Saikia, Uma Nahar.
Afiliação
  • Ramamoorthy S; Department of Pathology, NRI Medical College, Chinakakani, IND.
  • Garg S; Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, IND.
  • Mishra B; Department of Microbiology, All India Institute of Medical Sciences, Bhubaneswar, Bhubaneswar, IND.
  • Radotra BD; Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, IND.
  • Saikia UN; Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, IND.
Cureus ; 15(4): e37138, 2023 Apr.
Article em En | MEDLINE | ID: mdl-37153286
Coxsackievirus and adenovirus receptor (CAR) homologs have been identified in many species, and their proteins appeared to be highly conserved in evolution. While most of the human studies are about pathological conditions, the animal studies were more about the physiological and developmental functions of receptors. The expression of CAR is developmentally regulated, and its tissue localization is complex. Hence, we planned to study CAR expression in five different human organs at autopsy in different age groups. CAR expression was analyzed in the pituitary, heart, liver, pancreas, and kidney by immunohistochemistry, and CAR mRNA expression in the heart and pituitary by real-time PCR.  In the current study, CAR expression was strong in cells of the anterior pituitary, hepatocytes, and bile ducts in the liver, acini, and pancreas and distal convoluted tubule/collecting duct in the kidney, with uniform expression in all age groups. We have noted high CAR expression in fetuses and infantile hearts, which get reduced drastically in adults due to its presumed developmental role in intrauterine life studied in animal models. In addition, the receptor was expressed in glomerular podocytes around the period of fetus viability (37 weeks) but not in early fetuses and adults. We have hypothesized that this intermittent expression could be responsible for the intercellular contact normally formed between the podocytes during the developmental phase. Pancreatic islets also showed increased expression after the emergence of the viability period but not in early fetuses and adults, which might be related to an increase in fetal insulin secretion at that particular age group.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article