| Literature DB >> 30089414 |
Natasha P Clayton1, Alanna Burwell2, Heather Jensen1, Barbara F Williams1, Quashana D Brown1, Pamela Ovwigho1, Sreenivasa Ramaiahgari3, Tonia Hermon2, Darlene Dixon2.
Abstract
The use of three-dimensional (3-D) in vitro culture systems (spheroids, organoids) in biomolecular and drug discovery research has become increasingly popular. The popularity is due, in part, to a diminished reliance on animal bioassays and a desire to develop physiologically relevant cell culture systems that simulate the in vivo tissue microenvironment. Most evaluations of 3-D cultures are by confocal microscopy and high-content imaging; however, these technologies do not allow for detailed cellular morphologic assessments or permit basic hematoxylin and eosin histologic evaluations. There are few studies that have reported detailed processes for preparing 3-D cultures for paraffin embedding and subsequent use for histochemical or immunohistochemical staining. In an attempt to do so, we have developed a protocol to paraffin-embed human liver spheroids that can be sectioned with a microtome and mounted onto glass slides for routine histochemical and immunohistochemical staining and light microscopic evaluations.Entities:
Keywords: 3-D cultures; HepaRG spheroids; histochemistry; immunohistochemistry; in vitro; light microscopy; liver spheroids
Mesh:
Year: 2018 PMID: 30089414 PMCID: PMC6117202 DOI: 10.1177/0192623318789069
Source DB: PubMed Journal: Toxicol Pathol ISSN: 0192-6233 Impact factor: 1.902