Fluorescent dyes for lymphocyte migration and proliferation studies

Immunology and Cell Biology - Tập 77 Số 6 - Trang 499-508 - 1999
Christopher R. Parish1
1Division of Immunology and Cell Biology, John Curtin School of Medical Research, Australian National University Canberra Australian Capital Territory Australia

Tóm tắt

Fluorescent dyes are increasingly being exploited to track lymphocyte migration and proliferation. The present paper reviews the properties and performance of some 14 different fluorescent dyes that have been used during the last 20 years to monitor lymphocyte migration. Of the 14 dyes discussed, two stand out as being the most versatile in terms of long‐term tracking of lymphocytes and their ability to quantify lymphocyte proliferation. They are the intracellular covalent coupling dye carboxyfluorescein diacetate succinimidyl ester (CFSE) and the membrane inserting dye PKH26. Both dyes have the advantage that they can be used to track cell division, bothin vitroandin vivo, due to the progressive halving of the fluorescence intensity of the dyes in cells after each division. However, CFSE appears to have the edge over PKH26 based on homogeneity of lymphocyte staining and cost. Two other fluorescent dyes, although not suitable for lymphocyte proliferation studies, are valuable tracking dyes for short‐term (up to 3 day) lymphocyte migration experiments, namely the DNA‐binding dye Hoechst 33342 and the cytoplasmic dye calcein. In the future it is highly likely that additional fluorescent dyes, with different spectral properties to CFSE, will become available, as well as membrane inserting fluorescent dyes that more homogeneously label lymphocytes than PKH26.

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Tài liệu tham khảo

10.1098/rspb.1964.0001

10.1002/eji.1830060209

Rannie GH, 1977, An experimental comparison of radioactive labels with potential application to lymphocyte migration studies in patients., Clin. Exp. Immunol., 29, 509

Ford WL, 1978, Handbook of Experimental Immunology, 23.1

10.1002/eji.1830100310

10.1016/0022-1759(84)90364-8

10.1002/ar.1092130308

10.1016/0022-1759(80)90196-9

10.1016/0022-1759(90)90322-M

10.1016/0022-1759(91)90236-9

10.1016/S0091-679X(08)60547-6

10.1016/0022-1759(94)90236-4

10.1002/eji.1830160419

10.1038/icb.1987.58

Harp JA, 1990, Extravasation of lymphocytes via paracortical venules in sheep lymph nodes: Visualization using an intracellular fluorescent label., Vet. Immunol. Immunopathol., 31, 377

Maghazachi AA, 1990, Fate of intravenously administered rat lymphokine‐activated killer cells labeled with different markers., Cancer Immunol. Immunother., 24, 159

10.1002/eji.1830220804

10.1002/eji.1830251127

10.1038/icb.1997.77

10.1016/0165-5728(92)90008-9

Brenan M, 1987, Simultaneous determination of viable and dead fluorescently labelled lymphocytes., J. Immunol. Meth., 102, 147, 10.1016/S0022-1759(87)80020-0

10.1002/cyto.990130210

10.1016/0165-5728(94)90142-2

10.1016/0022-1759(89)90385-2

10.1016/0022-1759(94)90384-0

Weston SA, 1991, Modification of lymphocyte migration by mannans and phosphomannans: Different carbohydrate structures control entry of lymphocytes into spleen and lymph nodes., J. Immunol., 146, 4180, 10.4049/jimmunol.146.12.4180

Chiba K, 1998, FTY720, a novel immunosuppressant, induced sequestration of circulating mature lymphocytes by acceleration of lymphocyte homing in rats. I. FTY720 selectively decreases the number of circulating mature lymphocytes by acceleration of lymphocyte homing., J. Immunol., 160, 5037, 10.4049/jimmunol.160.10.5037

10.1046/j.1365-2567.1998.00639.x

10.1002/cyto.990130710

10.1016/0022-1759(80)90195-7

10.1021/bc00034a015

10.1084/jem.184.1.277

10.3109/08830189709068173

10.1002/(SICI)1521-4141(199803)28:03<1040::AID-IMMU1040>3.0.CO;2-9

10.1073/pnas.95.16.9488

10.1016/S1074-7613(00)80605-6

10.1006/cimm.1998.1341

Renno T, 1999, Apoptosis of superantigen‐activated T cells occurs preferentially after a discrete number of cell divisions in vivo., J. Immunol., 162, 6312, 10.4049/jimmunol.162.11.6312

10.1084/jem.183.5.2313

10.1172/JCI119873

10.1038/icb.1997.2

10.1002/(SICI)1097-0320(19980615)34:3<143::AID-CYTO4>3.0.CO;2-I

10.1046/j.1365-2141.1997.2823097.x

Khil LY, 1997, Insulin has a limited effect on the cell cycle progression in 3T3, L1 fibroblasts., Mol. Cells, 7, 742, 10.1016/S1016-8478(23)13373-5

10.1046/j.1472-765X.1997.00225.x

Bradbury MG, 1996, The immunosuppressive compound 2‐acetyl‐4‐tetrahydroxybutyl imidazole inhibits the allogeneic MLR by sequestration of a recirculating subpopulation of T cells., Immunology, 87, 80

10.1016/S0022-1759(97)00089-6

10.1016/S0016-5085(98)70141-6

10.1006/excr.1997.3900

10.1002/(SICI)1097-0185(199601)244:1<112::AID-AR11>3.0.CO;2-S

10.1016/0166-2236(89)90040-4

10.1083/jcb.114.5.929

10.1016/1047-8477(90)90109-P

10.1083/jcb.144.6.1271

Dittel BN, 1999, Presentation of the self antigen myelin basic protein by dendritic cells leads to experimental autoimmune encephalomyelitis., J. Immunol., 163, 32, 10.4049/jimmunol.163.1.32

10.1006/mvre.1993.1018

10.1007/BF00270034

10.1038/340167a0

Slezak SE, 1989, Fluorescent in vivo tracking of hematopoietic cells. Part I. Technical considerations., Blood, 74, 2172, 10.1182/blood.V74.6.2172.2172

10.1016/0008-8749(91)90339-D

10.1016/0145-2126(93)90153-C

10.1016/S0022-1759(98)00056-8

Boutonnat J, 1998, PKH26 probe in the study of the proliferation of chemoresistant leukemic sublines., Anticancer Res., 18, 4243

Hendrikx PJ, 1996, Homing of fluorescently labeled murine hematopoietic stem cells., Exp. Hematol., 24, 129

Wallace PK, 1993, Mechanisms of adoptive immunotherapy: Improved methods for in vivo tracking of tumor‐infiltrating lymphocytes and lymphokine‐activated killer cells., Cancer Res., 53, 2358

10.1002/(SICI)1097-0320(19990801)36:4<312::AID-CYTO5>3.0.CO;2-V

10.1016/0022-1759(94)90245-3

10.1093/intimm/7.10.1607

10.1046/j.1365-3083.1997.d01-430.x

10.1016/0022-1759(93)90113-L

10.1002/jlb.59.5.631