The costs of using unauthenticated, over-passaged cell lines: how much more data do we need?

被引:296
作者
Hughes, Peyton
Marshall, Damian
Reid, Yvonne
Parkes, Helen
Gelber, Cohava
机构
[1] ATCC, Manassas, VA
[2] LGC Limited, Teddington, Middlesex
[3] ATCC, Manassas, VA 20110
关键词
D O I
10.2144/000112598
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Increasing data demonstrate that cellular cross-contamination, misidentified cell lines, and the use of cultures at high-passage levels contribute to the generation of erroneous and misleading results as well as wasted research funds. Contamination of cell lines by other lines has been recognized and documented back to the 1950s. Based on submissions to major cell repositories in the last decade, it is estimated that between 18% and 36% of cell lines may be contaminated or misidentified. More recently, problems surrounding practices of over-subculturing cells are being identified. As a result of selective pressures and genetic drift, cell lines, when kept in culture too long, exhibit reduced or altered key functions and often no longer represent reliable models of their original source material. A review of papers showing significant experimental variances between low- and high-passage cell culture numbers, as well as contaminated lines, makes a strong case for using verified, tested cell lines at low- or defined passage numbers. In the absence of cell culture guidelines, mandates from the National Institutes of Health (NIH) and other funding agencies or journal requirements, it becomes the responsibility of the scientific community to perform due diligence to ensure the integrity of cell cultures used in research.
引用
收藏
页码:575 / +
页数:7
相关论文
共 58 条
[41]   Permeability characteristics of parental and clonal human intestinal Caco-2 cell lines differentiated in serum-supplemented and serum-free media [J].
Ranaldi, G ;
Consalvo, R ;
Sambuy, Y ;
Scarino, ML .
TOXICOLOGY IN VITRO, 2003, 17 (5-6) :761-767
[42]   CELL-LINE CROSS-CONTAMINATION OF U-397 [J].
REID, YA ;
MCGUIRE, L ;
ONEILL, K ;
MACY, M ;
CHEN, TR ;
MCCLINTOCK, P ;
DOROTINSKY, C ;
HAY, R .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 57 (05) :804-804
[43]   ACTIVE HEXOSE-TRANSPORT ACROSS CULTURED HUMAN CACO-2 CELLS - CHARACTERIZATION AND INFLUENCE OF CULTURE CONDITIONS [J].
RILEY, SA ;
WARHURST, G ;
CROWE, PT ;
TURNBERG, LA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1066 (02) :175-182
[44]   Comprehensive cytogenetic and molecular genetic characterization of the Tl-1 acute myeloid leukemia cell line reveals cross-contamination with K-562 cell line [J].
Rush, LJ ;
Heinonen, K ;
Mrózek, K ;
Wolf, BJ ;
Abdel-Rahman, M ;
Szymanska, J ;
Peltomäki, P ;
Kapadia, F ;
Bloomfield, CD ;
Caligiuri, MA ;
Plass, C .
BLOOD, 2002, 99 (05) :1874-1876
[45]   The Caco-2 cell line as a model of the intestinal barrier: influence of cell and culture-related factors on Caco-2 cell functional characteristics [J].
Sambuy, Y ;
Angelis, I ;
Ranaldi, G ;
Scarino, ML ;
Stammati, A ;
Zucco, F .
CELL BIOLOGY AND TOXICOLOGY, 2005, 21 (01) :1-26
[46]  
SICILIANO MJ, 1979, CANCER RES, V39, P919
[47]   DNA FINGERPRINTING TRANSFORMS THE ART OF CELL AUTHENTICATION [J].
STACEY, GN ;
BOLTON, BJ ;
DOYLE, A .
NATURE, 1992, 357 (6375) :261-262
[48]   Cell contamination leads to inaccurate data: we must take action now [J].
Stacey, GN .
NATURE, 2000, 403 (6768) :356-356
[49]  
Stulberg C. S., 1973, Contamination in tissue culture,, P1
[50]   IDENTIFICATION OF CELLS IN CULTURE [J].
STULBERG, CS ;
PETERSON, WD ;
SIMPSON, WF .
AMERICAN JOURNAL OF HEMATOLOGY, 1976, 1 (02) :237-242