A NEW SUBSTRAIN DERIVED FROM HEP-2 FOR THE DETECTION OF ANTI-NUCLEAR ANTIBODIES
A new substrain of cells, named Ban, was obtained from the human epidermoid carcinoma 2 (HEp-2) cell line. The Ban cells, which are larger than HEp-2 cells were isolated using a cell sorter after seeding HEp-2 cells by the limited dilution method. Not only the cell size but also the size of the nucl...
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Published in | TISSUE CULTURE RESEARCH COMMUNICATIONS Vol. 17; no. 3; pp. 95 - 100 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
The Japanese Tissue Culture Association
1998
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Abstract | A new substrain of cells, named Ban, was obtained from the human epidermoid carcinoma 2 (HEp-2) cell line. The Ban cells, which are larger than HEp-2 cells were isolated using a cell sorter after seeding HEp-2 cells by the limited dilution method. Not only the cell size but also the size of the nucleus of Ban cells was found to be larger than that of HEp-2 cells, and these characteristics were maintained for more than 7 months (46 passages). The chromosome frequency distribution of Ban cells was about 1.5 times greater than that of HEp-2 cells. When cell number were examined comparing Ban cells (50 passages) and HEp-2 cells, no significant difference in cell growth was observed for up to 7 days. Ban cells are useful for detection of anti-nuclear antibodies since these cells display 5 kinds of nuclear staining patterns as in the case of HEp-2 cells. However, the relative fluorescence intensity of Ban cells was greater than that of HEp-2 cells upon staining with anti-cytoplasmic antibodies. |
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AbstractList | A new substrain of cells, named Ban, was obtained from the human epidermoid carcinoma 2 (HEp-2) cell line. The Ban cells, which are larger than HEp-2 cells were isolated using a cell sorter after seeding HEp-2 cells by the limited dilution method. Not only the cell size but also the size of the nucleus of Ban cells was found to be larger than that of HEp-2 cells, and these characteristics were maintained for more than 7 months (46 passages). The chromosome frequency distribution of Ban cells was about 1.5 times greater than that of HEp-2 cells. When cell number were examined comparing Ban cells (50 passages) and HEp-2 cells, no significant difference in cell growth was observed for up to 7 days. Ban cells are useful for detection of anti-nuclear antibodies since these cells display 5 kinds of nuclear staining patterns as in the case of HEp-2 cells. However, the relative fluorescence intensity of Ban cells was greater than that of HEp-2 cells upon staining with anti-cytoplasmic antibodies. |
Author | ISHI, Akira BAN, Fumihiko TSUBOI, Isami MACHIDA, Kunimitu KENMOTSU, Masashi TAGUCHI, Michihiro INAGAKI, Kouichi TAZAWA, Tadashi |
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References | 9) Yoshida A, Ohyashiki K, Ochi H, Gibas Z, Pontes E, Prout R., Huben R, Sandberg A.: Cytogenetic studies of tumor tissue from patients with nonfamilial renal cell carcinoma. Cancer Res. 46, 2139-2147, 1986. 6) Miyawaki S.: Antinuclear antibody. Medical Technology 18, 570-573, 1990. 2) Toolan, H. W.: Transplantable human neoplasms maintained in cortisone-treated laboratory animals: H. S. #1; H. Ep. #1; H. Ep. #2; H. Ep, #3; and H. Emb. Rh. #1, 14. Cancer Res. 14, 660-666, 1954. 3) Beutner H, Kransny A, Chorzelski T. P, Rodnon G, Jablonska S, Kumar V.: Evaluation of methods for detection of anticentromere antibodies and other antinuclear antibodies. J. Am. Acad. Dermatol. 12, 289-295, 1985. 10) [ANA test - BML] the attached paper on the diagnostic reagent-, license No. 21000AMZ00173000. 7) Moteki S, Kato Y, Ishikawa H, Honda S, Yoshida H. Sato K, Morito T.: Detection of antinuclear antibodies and anti-cytoplasmica ntibodiesb y immunofluorescense method using Hep-2 cells. Jpn. J. Clin. Pathol., 37, 517-52, 1989. 5) Moroi Y, Peebles C, Fritzler M. J, Steigerwald J, Tan E. M. Autoantibody to centromere (kinetochore) in scleroderma sera. Proc. Natl. Acad. Sci. USA 77, 1627-1631, 1979. 4) Miller M, Littlejohn O, Jones W, Strand H.: Clinical comparison of cultured human epithelial cells and rat liver as substrates for the fluorescent antinuclear antibody test. J. Rheumatol. 12, 265-269, 1985. 8) Watanabe S, Miyawaki,S.: Detectiono f antinuclear antibodies using HEp-2 cells as nuclear substrates by indirect immunofluorescence antibody technique. Jpn. J. Clin. Pathol. 35, 61-66, 1987. 1) Tan M.: Autoantibodies to nuclear antigens (ANA): Their immunobiology and properties of murine hemopoietic cells. Blood Cells 6, 391-407, 1982. |
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Title | A NEW SUBSTRAIN DERIVED FROM HEP-2 FOR THE DETECTION OF ANTI-NUCLEAR ANTIBODIES |
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