Renal proximal tubular epithelial cells: review of isolation, characterization, and culturing techniques.
Acute kidney injury
Cell isolation
Cell morphology
Chronic kidney disease
Cultured cells
Lab-on-a-chip device
Pharmacokinetics
Proximal renal tubule
Stem cells
Journal
Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
received:
06
08
2020
accepted:
03
11
2020
pubmed:
11
11
2020
medline:
13
7
2021
entrez:
10
11
2020
Statut:
ppublish
Résumé
The kidney is a complex organ, comprised primarily of glomerular, tubular, mesangial, and endothelial cells, and podocytes. The fact that renal cells are terminally differentiated at 34 weeks of gestation is the main obstacle in regeneration and treatment of acute kidney injury or chronic kidney disease. Furthermore, the number of chronic kidney disease patients is ever increasing and with it the medical community should aim to improve existing and develop new methods of renal replacement therapy. On the other hand, as polypharmacy is on the rise, thought should be given into developing new ways of testing drug safety. A possible way to tackle these issues is with isolation and culture of renal cells. Several protocols are currently described to isolate the desired cells, of which the most isolated are the proximal tubular epithelial cells. They play a major role in water homeostasis, acid-base control, reabsorption of compounds, and secretion of xenobiotics and endogenous metabolites. When exposed to ischemic, toxic, septic, or obstructive conditions their death results in what we clinically perceive as acute kidney injury. Additionally, due to renal cells' limited regenerative potential, the profibrotic environment inevitably leads to chronic kidney disease. In this review we will focus on human proximal tubular epithelial cells. We will cover human kidney culture models, cell sources, isolation, culture, immortalization, and characterization subdivided into morphological, phenotypical, and functional characterization.
Identifiants
pubmed: 33170426
doi: 10.1007/s11033-020-05977-4
pii: 10.1007/s11033-020-05977-4
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
9865-9882Subventions
Organisme : Slovenian Research Agency
ID : P3-0036, L4-1843
Organisme : University Medical Centre Maribo
ID : IRP 2018/01-07