Cellular observations enabled by microculture: paracrine signaling and population demographics.

Imagen de Maribella Domenech
PDF versionPDF version
TítuloCellular observations enabled by microculture: paracrine signaling and population demographics.
Publication TypeJournal Article
Year of Publication2009
AutoresDomenech, M, Yu, H, Alexander, CM, Beebe, DJ
Secondary AuthorsWarrick, J
Tertiary AuthorsBadders, NM, Meyvantsson, I
JournalIntegr Biol (Camb)
Volume1
Issue3
Pagination267-74
Date Published2009 Mar
ISSN1757-9708
Palabras claveCell Line, Coculture Techniques, Equipment Design, Equipment Failure Analysis, Humans, Macrophages, Male, Microfluidic Analytical Techniques, Paracrine Communication, Prostatic Neoplasms
Abstract

The cellular microenvironment plays a critical role in shaping and directing the process of communication between the cells. Soluble signals are responsible for many cellular behaviors such as cell survival, proliferation and differentiation. Despite the importance of soluble signals, canonical methods are not well suited to the study of soluble factor interactions between multiple cell types. Macro-scale technology often puts cells into a convective environment that can wash away and dilute soluble signals from their targets, minimizing local concentrations of important factors. In addition, current methods such as transwells, require large numbers of cells and are limited to studying just two cell types. Here, we present data supporting the use of microchannels to study soluble factor signaling providing improved sensitivity as well as the ability to move beyond existing co-culture and conditioned medium paradigms. In addition, we present data suggesting that microculture can be used to unmask effects of population demographics. In this example the data support the hypothesis that a growth promoting subpopulation of cells exists in the mouse mammary gland.

DOI10.1039/b823059e
Alternate JournalIntegr Biol (Camb)
PubMed ID20011455
PubMed Central IDPMC2791414
Grant List5T15LM007359 / LM / NLM NIH HHS / United States
K25 CA104162 / CA / NCI NIH HHS / United States
K25 CA104162 / CA / NCI NIH HHS / United States
K25 CA104162-05 / CA / NCI NIH HHS / United States