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...

Full description

Saved in:
Bibliographic Details
Published inTISSUE CULTURE RESEARCH COMMUNICATIONS Vol. 17; no. 3; pp. 95 - 100
Main Authors TSUBOI, Isami, TAGUCHI, Michihiro, KENMOTSU, Masashi, BAN, Fumihiko, MACHIDA, Kunimitu, INAGAKI, Kouichi, ISHI, Akira, TAZAWA, Tadashi
Format Journal Article
LanguageEnglish
Published The Japanese Tissue Culture Association 1998
Subjects
Online AccessGet full text

Cover

Loading…
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.
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
Author_xml – sequence: 1
  fullname: TSUBOI, Isami
  organization: BML General Laboratory, BML Inc
– sequence: 2
  fullname: TAGUCHI, Michihiro
  organization: BML General Laboratory, BML Inc
– sequence: 3
  fullname: KENMOTSU, Masashi
  organization: BML General Laboratory, BML Inc
– sequence: 4
  fullname: BAN, Fumihiko
  organization: BML General Laboratory, BML Inc
– sequence: 5
  fullname: MACHIDA, Kunimitu
  organization: BML General Laboratory, BML Inc
– sequence: 6
  fullname: INAGAKI, Kouichi
  organization: BML General Laboratory, BML Inc
– sequence: 7
  fullname: ISHI, Akira
  organization: BML General Laboratory, BML Inc
– sequence: 8
  fullname: TAZAWA, Tadashi
  organization: BML General Laboratory, BML Inc
BookMark eNo9kE1OwzAYRC1UJNrCAdj5Ai7-7Li2l2nqtJFKjNIUlpZxHGhUCkq64fb8s5mn0ZNmMRM0Or4eI0LXQGcACaib7hQ8aAUzkDPutDhDY1AKCJc0GaEx1cAIn_P5BZoMQ0epUEzAGNkUl-YBb3eLbV2lRYmXpiruzRLnlb3Fa3NHGM5theu1-VS1yerCltjmOC3rgpS7bGPS6rss7LIw20t03vrDEK9-OUW73NTZmmzsqsjSDemYSBiRtGFBNq0KDWsEk7oNSvs2kcD9I0QNQcBcCi8oE5QLYFHT0DY8No1QXEo-RenPbjec_FN0b_3-xffvzvenfThE93eHA-n4V2jx78Kz71088g_IWVZP
ContentType Journal Article
Copyright The Japanese Tissue Culture Association
Copyright_xml – notice: The Japanese Tissue Culture Association
DOI 10.11418/jtca1981.17.3_95
DatabaseTitleList
DeliveryMethod fulltext_linktorsrc
EISSN 1881-3704
EndPage 100
ExternalDocumentID article_jtca1981_17_3_17_95_article_char_en
GroupedDBID 2WC
ACGFS
ALMA_UNASSIGNED_HOLDINGS
JSF
KQ8
OK1
RJT
ID FETCH-LOGICAL-j2542-70d2c7df8cd2d5279fc89af4713ab1e91c51675a502503512e90cfd3edd583773
ISSN 0912-3636
IngestDate Wed Apr 05 06:15:07 EDT 2023
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-j2542-70d2c7df8cd2d5279fc89af4713ab1e91c51675a502503512e90cfd3edd583773
OpenAccessLink https://www.jstage.jst.go.jp/article/jtca1981/17/3/17_95/_article/-char/en
PageCount 6
ParticipantIDs jstage_primary_article_jtca1981_17_3_17_95_article_char_en
PublicationCentury 1900
PublicationDate 1998
PublicationDateYYYYMMDD 1998-01-01
PublicationDate_xml – year: 1998
  text: 1998
PublicationDecade 1990
PublicationTitle TISSUE CULTURE RESEARCH COMMUNICATIONS
PublicationTitleAlternate Tiss. Cult. Res. Commun.
PublicationYear 1998
Publisher The Japanese Tissue Culture Association
Publisher_xml – name: The Japanese Tissue Culture Association
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.
References_xml
SSID ssj0058251
ssib002484537
Score 1.4273978
Snippet 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...
SourceID jstage
SourceType Publisher
StartPage 95
SubjectTerms anti-nuclear antibody
cytoplasmic staining pattern
HEp-2
large cell
large nuclei
substrain
Title A NEW SUBSTRAIN DERIVED FROM HEP-2 FOR THE DETECTION OF ANTI-NUCLEAR ANTIBODIES
URI https://www.jstage.jst.go.jp/article/jtca1981/17/3/17_95/_article/-char/en
Volume 17
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
ispartofPNX TISSUE CULTURE RESEARCH COMMUNICATIONS, 1998/09/30, Vol.17(3), pp.95-100
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3Nk5MwFM_U9eLFWUcdvycHbwy1IaTA3lhKLbqAbkH3xkACY-ts6-y2F_8z_ztfQqCoe3D1kqFp00nm_XhfeR8IvQahz1hlW2bFgQXajeCmx6Ujv7JpbQtqcxVVGSfTRW6_u2AXo9GPQdTSfleN-fcb80r-haowB3SVWbK3oGz_pzABz0BfGIHCMP4VjX0jCT8by_xUdj6OEmMGVtmncGbMz9PYWIQfTMsAI09F9czCLFTxIjLMx0-yyEzy4Cz0z9WH07RXC7WimkXLZR4aQX6m4iK6eyUjSOMYbEadftzb_bCHNFL85rq8XPXT_ts8WERdeP7qy-pq23P4MIlTWNcmDF3Lnk69a8BXsQfz_SWs-Lo9OCZkpl4PIpXUBqJettAEyEn86AKh9R-g075IWTlxSnVN7JYTuy4B7tf2Ju5ZtTOAJB3w3bZRp5bgRNU-vUE42ERmPKx3vCSeS8bEGdOiW_lLzW1N0aL7aUGcgsrBY0X3ncyKAxDeQXct4HEymvT9x6El59rsYPszmSGsyj7qk-oLdrmlN79vCJShNZgGXVih0nSyY3RfmyjYb3fwAI3qzUOU-hiwhnusYY01LLGGFdYwYA0D1nCPNZzO8RBr-IC1Ryifh1mwMHUzDnNtMXiXnYmwuCMalwtLMDhyw12vbEC3oWVFao9wRsD4LJlUqimokbU34Y2gtRDMpY5DH6OjzXZTP0GY1I3w5IV8UwpbVHVl2bSalKIhIOxKNn2KTtrzF9_aiivFLejx7H8WP0f32pxT6WJ7gY52V_v6JSidu-qVIu9PckF0uw
link.rule.ids 315,783,787,4031,27935,27936,27937
linkProvider Colorado Alliance of Research Libraries
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+NEW+SUBSTRAIN+DERIVED+FROM+HEP-2+FOR+THE+DETECTION+OF+ANTI-NUCLEAR+ANTIBODIES&rft.jtitle=TISSUE+CULTURE+RESEARCH+COMMUNICATIONS&rft.au=TSUBOI%2C+Isami&rft.au=TAGUCHI%2C+Michihiro&rft.au=KENMOTSU%2C+Masashi&rft.au=BAN%2C+Fumihiko&rft.date=1998&rft.pub=The+Japanese+Tissue+Culture+Association&rft.issn=0912-3636&rft.eissn=1881-3704&rft.volume=17&rft.issue=3&rft.spage=95&rft.epage=100&rft_id=info:doi/10.11418%2Fjtca1981.17.3_95&rft.externalDocID=article_jtca1981_17_3_17_95_article_char_en
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0912-3636&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0912-3636&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0912-3636&client=summon