In vitro cyst formation of ADPKD cells

• Published in: Methods in Kidney Cell Biology Part A Vol. 153; pp. 93 - 111
• Main Authors: Sharma, Madhulika, Reif, Gail A, Wallace, Darren P
• Format: Book Chapter Journal Article
• Language: English
• Published: United States Elsevier Science & Technology 2019
• Subjects: Animals; Collagen - metabolism; Culture Media - metabolism; Cyclic AMP - agonists; Cyclic AMP - metabolism; Dogs; Epithelial Cells - metabolism; Epithelial Cells - pathology; Humans; Intravital Microscopy - instrumentation; Intravital Microscopy - methods; Madin Darby Canine Kidney Cells; Neurophysins - metabolism; Polycystic Kidney, Autosomal Dominant - etiology; Polycystic Kidney, Autosomal Dominant - pathology; Primary Cell Culture - instrumentation; Primary Cell Culture - methods; Protein Precursors - metabolism; Vasopressins - metabolism; Renal epithelial cells; In vitro models; Proliferation; Fluid secretion; Autosomal dominant polycystic kidney disease
• ISBN: 0128170824; 9780128170823
• ISSN: 0091-679X
• DOI: 10.1016/bs.mcb.2019.05.008

Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic disorder characterized by the relentless growth of numerous fluid-filled cysts in the kidneys. Mutations in PKD1 and PKD2, genes that encode polycystin 1 and 2, respectively, are responsible for most cases of ADPKD. Currently, the cellular mechanisms responsible for cyst formation remain poorly understood. In vitro models have been used by researchers to investigate cellular processes for cyst formation in carefully controlled experimental conditions. Madin-Darby canine kidney (MDCK) cells, a distal tubule epithelial cell line, were first used to form 3-dimensional (3-D) cysts within a hydrated collagen gel. This method was applied to epithelial cells cultured from cysts of human ADPKD kidneys, allowing investigators to study cellular mechanisms for cyst growth using cells that harbor the genetic mutations responsible for ADPKD in humans. Studies using ADPKD in vitro cysts have provided insight into cellular processes regulating cell proliferation, fluid secretion, and cell polarity. These assays were used to demonstrate the central role of cAMP agonists, such as arginine vasopressin, on cyst growth; and to test the effectiveness of potential therapeutic agents, including tolvaptan. Results obtained from in vitro cyst experiments demonstrate the translational value of cell model systems for investigating the mechanisms for cyst formation in human ADPKD. In this chapter, we describe protocols for growing ADPKD cells in a 3-D in vitro cyst assay and measuring total cyst volume by microscopy and image analysis.