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Journal of Nippon Medical School

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Immunocytochemical Analysis of a Three-dimensional Spheroidal Culture System

Yoko Matsuda, Toshiyuki Ishiwata and Zenya Naito

Department of Integrative Pathology, Graduate School of Medicine, Nippon Medical School


Three-dimensional (3D) cell cultures are expected to mimic in vivo environments. The NanoCulture plate (Scivax Corporation, Kawasaki) allows the formation of 3D spheroids1, 2. The cytoskeletal proteins are considered to be important regulators of cellular morphology and structure. Among the cytoskeletal proteins, fibrillar actin (F-actin) is a main component of microfilament proteins, and α-tubulin is the major protein forming microtubules in cells. Therefore, in this study, we used NanoCulture plates to examine the expression patterns of F-actin and α-tubulin in PANC-1, a human pancreatic cancer cell line. The cells were stained with polyclonal antibodies against α-tubulin antibody and with Alexa 568-labeled phalloidin to detect F-actin. Eighty-eight horizontal images (Fig. 1) were obtained at 0.25-μm intervals with a confocal laser microscope (TE2000-E, Nikon Instech Co., Ltd., Tokyo). In horizontal images, the expression of F-actin was observed at the periphery of cells (Fig. 2A-C, red), and strong F-actin expression was observed on the grids of the NanoCulture plate at the levels of cells nearest the plate (Fig. 2C, arrows and inset). The expression of α-tubulin was observed in the cytoplasm of cells in 3D cultures (Fig. 2A-C, green). Vertical images revealed that the cells piled up in 3D culture (Fig. 2D) and that cells formed actin-rich cell projections that attached to the surface (Fig. 2D arrows). The 3D images (Fig. 3) revealed the different expression patterns of cytoskeletal proteins in the spheroids as well as the relationship between cell-to-cell interactions in these cytoskeletal proteins. The 3D culture enabled analysis of the morphological changes and the cell-to-cell interactions in spheroids, which cannot be observed with 2D cultures. The 3D spheroidal culture system is a useful method for cell imaging and can mimic in vivo environments.

J Nippon Med Sch 2011; 78: 206-207

Correspondence to
Zenya Naito, MD, PhD, Departments of Pathology, Integrative Oncological Pathology, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113-8602, Japan
naito@nms.ac.jp