Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Rokstad, AM; Gustafsson, BI; Espevik, T; Bakke, I; Pfragner, R; Svejda, B; Modlin, IM; Kidd, M.
Microencapsulation of small intestinal neuroendocrine neoplasm cells for tumor model studies.
Cancer Sci. 2012; 103(7):1230-1237 Doi: 10.1111/j.1349-7006.2012.02282.x [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Pfragner Roswitha
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Basic cancer research is dependent on reliable in vitro and in vivo tumor models. The serotonin (5-HT) producing small intestinal neuroendocrine tumor cell line KRJ-1 has been used in in vitro proliferation and secretion studies, but its use in in vivo models has been hampered by problems related to the xeno-barrier and tumor formation. This may be overcome by the encapsulation of tumor cells into alginate microspheres, which can function as bioreactors and protect against the host immune system. We used alginate encapsulation of KRJ-1 cells to achieve long-term functionality, growth and survival. Different conditions, including capsule size, variations in M/G content, gelling ions (Ca(2+) /Ba(2+)) and microcapsule core properties, and variations in KRJ-1 cell condition (single cells/spheroids) were tested. Viability and cell growth was evaluated with MTT, and confocal laser scanner microscopy combined with LIVE/DEAD viability stains. 5-HT secretion was measured to determine functionality. Under all conditions, single cell encapsulation proved unfavorable due to gradual cell death, while encapsulation of aggregates/spheroids resulted in surviving, functional bioreactors. The most ideal spheroids for encapsulation were 200-350 μm. Long-term survival (>30 days) was seen with solid Ca(2+) /Ba(2+) microbeads and hollow microcapsules. Basal 5-HT secretion was increased (sixfold) after hollow microcapsule encapsulation, while Ca(2+) /Ba(2+) microbeads was associated with normal basal secretion and responsiveness to cAMP/PKA activation. In conclusion, encapsulation of KRJ-1 cells into hollow microcapsules produces a bioreactor with a high constitutively activate basal 5-HT secretion, while Ca(2+) /Ba(2+) microbeads provide a more stable bioreactor similar to non-encapsulated cells. Alginate microspheres technology can thus be used to tailor different functional bioreactors for both in vitro and in vivo studies. © 2012 Japanese Cancer Association.
Find related publications in this database (using NLM MeSH Indexing)
Adrenergic beta-Agonists - pharmacology
Alginates - chemistry
Alginates - pharmacology
Barium - chemistry
Barium - pharmacology
Biocompatible Materials - chemistry
Biocompatible Materials - pharmacology
Calcium - chemistry
Calcium - pharmacology
Capsules -
Cell Line, Tumor -
Cell Proliferation - drug effects
Cell Survival - drug effects
Colforsin - pharmacology
Glucuronic Acid - chemistry
Glucuronic Acid - pharmacology
Hexuronic Acids - chemistry
Hexuronic Acids - pharmacology
Humans -
Intestine, Small - metabolism
Intestine, Small - pathology
Isoproterenol - pharmacology
Microscopy, Confocal -
Microspheres -
Models, Biological -
Neuroendocrine Tumors - metabolism
Neuroendocrine Tumors - pathology
Serotonin - metabolism
Spheroids, Cellular - drug effects
Spheroids, Cellular - metabolism
Spheroids, Cellular - pathology
Time Factors -

© Med Uni Graz Impressum