2002
DOI: 10.1002/0471142301.ns0615s19
|View full text |Cite
|
Sign up to set email alerts
|

Preparation and Maintenance of Organotypic Cultures for Multi‐Electrode Array Recordings

Abstract: Recording from neuronal cultures with multi-electrode arrays (MEAs) provides a powerful tool for studying neuronal activity with many neurons simultaneously in vitro. This unit describes the detailed steps necessary for growing organotypic cultures on MEAs and the typical neuronal activity that is obtained with this methodology.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
11
0

Year Published

2003
2003
2020
2020

Publication Types

Select...
8
1

Relationship

4
5

Authors

Journals

citations
Cited by 13 publications
(11 citation statements)
references
References 12 publications
0
11
0
Order By: Relevance
“…Each MEA covered ~1 mm of the cortical depth of a coronal slice and a VTA slice was positioned at the ventral border of the cortex, juxtaposing the white matter. Coculturing of slices was described in detail previously (Plenz and Kitai, 1998; Karpiak and Plenz, 2002). In short, a sterile chamber was attached to the MEA, which allowed for cultivation and repeated recording from single cocultures for many weeks.…”
Section: Methodsmentioning
confidence: 99%
“…Each MEA covered ~1 mm of the cortical depth of a coronal slice and a VTA slice was positioned at the ventral border of the cortex, juxtaposing the white matter. Coculturing of slices was described in detail previously (Plenz and Kitai, 1998; Karpiak and Plenz, 2002). In short, a sterile chamber was attached to the MEA, which allowed for cultivation and repeated recording from single cocultures for many weeks.…”
Section: Methodsmentioning
confidence: 99%
“…Each MEA consisted of a square (5 ϫ 5 cm) plate of glass with a circular glass well attached to the center that functioned as a culture chamber (Karpiak and Plenz, 2002). The center of the well contained a square array of 60 microelectrodes made of titanium nitride (8 ϫ 8 grids with the corners missing).…”
Section: Preparation Of Measmentioning
confidence: 99%
“…Organotypic cultures from slices of rat cortex were prepared in accordance with NIH guidelines (Plenz and Kitai, 1998;Karpiak and Plenz, 2002). In short, coronal sections from rat brains at postnatal day 0-2 (P0-2; Sprague Dawley, Taconic Farms, MD, USA) were cut at a thickness of 350 μm.…”
Section: Preparation Of Organotypic Cultures On the Multielectrode Armentioning
confidence: 99%