A flow cytometric comparison of Indo-1 to fluo-3 and Fura Red excited with low power lasers for detecting Ca2+ flux

被引:28
作者
Bailey, Sheree
Macardle, Peter J.
机构
[1] Flinders Med Ctr, Dept Immunol Allergy & Arthrit, Adelaide, SA 5042, Australia
[2] Flinders Univ S Australia, Adelaide, SA 5042, Australia
关键词
flow cytometry; calcium channels; calcium flux; Indo-1; Fura Red; fluo-3;
D O I
10.1016/j.jim.2006.02.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Indo-1 and high-power water-cooled lasers have been the standard for flow cytometric based Ca2+ flux measurements. With advances in technology and the availability of low-power air-cooled lasers, there is interest in alternative protocols. Here, we have compared Indo-1 with the combination of fluo-3 and Fura Red calcium indicator dyes using low-power air-cooled lasers as the excitation source. The reagents were examined in parallel to detect Ca2+ flux in peripheral blood T lymphocytes and in a T lymphoblastoid cell line. Ca2+ flux was detected with a FACSVantage SE equipped with an Omnichrome Series 74 Helium-Cadmium, or a Spectra Physics 177-G1202 Argon ion air-cooled laser. Following determination of optimal loading conditions, Ca2+ flux was examined in response to membrane receptor stimulation or intracellular Ca2+ mobilization. Dose dependent Ca2+ flux to anti-CD3 and thapsigargin was detected with either Indo-1 or with fluo-3 and Fura Red. The profile of the Ca2+ flux detected by Indo-1 or with fluo-3 and Fura Red appeared similar, with the combination of fluo-3 and Fura Red more sensitive under the particular test conditions. The results clearly demonstrated that Indo-1 could be usefully excited with a low-power air-cooled laser. The alternative use of fluo-3 and Fura Red does not require the availability of a UV capable laser and produced equivalent data. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:220 / 225
页数:6
相关论文
共 15 条
[1]   A COMPARISON OF LOW-POWER HELIUM-CADMIUM AND ARGON ULTRAVIOLET-LASERS IN COMMERCIAL FLOW CYTOMETERS [J].
BIGLER, RD .
CYTOMETRY, 1987, 8 (05) :441-444
[2]   Calcium signalling: More messengers, more channels, more complexity [J].
Bootman, MD ;
Berridge, MJ ;
Roderick, HL .
CURRENT BIOLOGY, 2002, 12 (16) :R563-R565
[3]   Analysis of free intracellular calcium by flow cytometry: Multiparameter and pharmacologic applications [J].
Burchiel, SW ;
Edwards, BS ;
Kuckuck, FW ;
Lauer, FT ;
Prossnitz, ER ;
Ransom, JT ;
Sklar, LA .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 2000, 21 (03) :221-230
[4]   UV LASERS FOR FLOW CYTOMETRIC ANALYSIS - HECD VERSUS ARGON-LASER EXCITATION [J].
GOLLER, B ;
KUBBIES, M .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1992, 40 (04) :451-456
[5]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[6]   IMPROVED BRDURD-HOECHST BIVARIATE CELL KINETIC-ANALYSIS BY HELIUM-CADMIUM SINGLE LASER EXCITATION [J].
KUBBIES, M ;
GOLLER, B ;
VANBOCKSTAELE, DR .
CYTOMETRY, 1992, 13 (07) :782-786
[7]   Analysis of the cord blood T lymphocyte response to superantigen [J].
Macardle, PJ ;
Wheatland, L ;
Zola, H .
HUMAN IMMUNOLOGY, 1999, 60 (02) :127-139
[8]   USE OF FLUO-3 TO MEASURE CYTOSOLIC CA-2+ IN PLATELETS AND NEUTROPHILS - LOADING CELLS WITH THE DYE, CALIBRATION OF TRACES, MEASUREMENTS IN THE PRESENCE OF PLASMA, AND BUFFERING OF CYTOSOLIC CA-2+ [J].
MERRITT, JE ;
MCCARTHY, SA ;
DAVIES, MPA ;
MOORES, KE .
BIOCHEMICAL JOURNAL, 1990, 269 (02) :513-519
[9]  
MINTA A, 1989, J BIOL CHEM, V264, P8171
[10]   IMPROVED SENSITIVITY IN FLOW CYTOMETRIC INTRACELLULAR IONIZED CALCIUM MEASUREMENT USING FLUO-3 FURA RED FLUORESCENCE RATIOS [J].
NOVAK, EJ ;
RABINOVITCH, PS .
CYTOMETRY, 1994, 17 (02) :135-141