scholarly journals Analysis of activated human lymphocytes membrane antigens by dual laser flow cytometry

1983 ◽  
Vol 6 (6) ◽  
pp. 523-534
Author(s):  
Yoshinobu Matsuo ◽  
Mitsuo Yokoyama ◽  
Katsumi Kinoshita ◽  
Yoshihiko Nagata ◽  
Kazuhiro Fujita
2015 ◽  
Vol 87 (12) ◽  
pp. 1070-1078 ◽  
Author(s):  
Matus Durdik ◽  
Pavol Kosik ◽  
Jan Gursky ◽  
Lenka Vokalova ◽  
Eva Markova ◽  
...  

Cytometry ◽  
1991 ◽  
Vol 12 (2) ◽  
pp. 167-171 ◽  
Author(s):  
Cynthia A. Sanders ◽  
David M. Yajko ◽  
Patricia S. Nassos ◽  
William C. Hyun ◽  
Mack J. Fulwyler ◽  
...  

1995 ◽  
Author(s):  
Harald Schaefer ◽  
Wolfgang Beisker ◽  
Christian Steinberg

2004 ◽  
Vol 11 (4) ◽  
pp. 795-798 ◽  
Author(s):  
E. C. Soethout ◽  
K. E. Müller ◽  
A. J. M. van den Belt ◽  
V. P. M. G. Rutten

ABSTRACT A method is proposed to identify leukocyte subpopulations in bovine bronchoalveolar lavage fluid by dual-laser flow cytometry. The technique uses several parameters, i.e., exclusion of highly autofluorescent alveolar macrophages and inclusion of leukocytes on the basis of labeling by specific antibodies and light scatter characteristics.


2007 ◽  
Vol 2 (1) ◽  
pp. 187-190 ◽  
Author(s):  
Ingrid Schmid ◽  
Christel Uittenbogaart ◽  
Beth D Jamieson

2010 ◽  
Vol 32 (5-6) ◽  
pp. 373-383
Author(s):  
Alessandra Donadini ◽  
Massimo Maffei ◽  
Antonio Cavallero ◽  
Monica Pentenero ◽  
Davide Malacarne ◽  
...  

Oral potentially malignant lesions (OPMLs) with dysplasia and aneuploidy are thought to have a high risk of progression into oral squamous cell carcinomas (OSCCs). Non-dysplastic “oral distant fields” (ODFs), characterized by clinically normal appearing mucosa sited at a distance from co-existing OPMLs, and non-dysplastic OPMLs may also represent an early pre-cancerous state. ODFs, OPMLs without and with dysplasia and OSCCs were investigated by high resolution DNA content flow cytometry (FCM). ODFs and OPMLs without dysplasia were DNA aneuploid respectively in 7/82 (8.5%) and 25/109 (23%) cases. “True normal oral mucosa” and human lymphocytes from healthy donors were DNA diploid in all cases and were used as sex specific DNA diploid controls. Dysplastic OPMLs and OSCCs were DNA aneuploid in 12/26 (46%) and 12/13 (92%) cases. The DNA aneuploid sublines were characterized by the DNA Index (DI ≠ 1). Aneuploid sublines in ODFs and in non-dysplastic and dysplastic OPMLs were near-diploid (DI < 1.4) respectively in all, 2/3 and 1/3 of the cases. DNA aneuploid OSCCs, instead, were characterized prevalently by multiple aneuploid sublines (67%), which were commonly (57%) high-aneuploid (DI ≥ 1.4). DNA near-diploid aneuploid sublines in ODFs and OPMLs appear as early events of the oral carcinogenesis in agreement with the concept of field effect. Near-diploid aneuploidization is likely to reflect mechanisms of loss of symmetry in the chromosome mitotic division. High DNA aneuploid and multiple sublines in OPMLs with dysplasia and OSCCs suggest, instead, mechanisms of “endoreduplication” of diploid and near-diploid aneuploid cells and chromosomal loss. High resolution DNA FCM seems to enable the separation of subsequent progression steps of the oral carcinogenesis.


Blood ◽  
1991 ◽  
Vol 78 (4) ◽  
pp. 1056-1061 ◽  
Author(s):  
S Fargion ◽  
AL Fracanzani ◽  
B Brando ◽  
P Arosio ◽  
S Levi ◽  
...  

Interactions between human recombinant H- and L-ferritins and human lymphocytes were studied in vitro by direct binding assays and by flow cytometry. L-ferritin did not cause detectable specific binding, whereas H-ferritin showed a specific and saturable binding that increased markedly in phytohemagglutinin (PHA)-stimulated cells. This ferritin bound up to 30% of CD4+ and CD8+ T-lymphocytes and most B cells, indicating that expression of ferritin binding sites is not related to cell lineage or function. Dual-color flow cytometry experiments showed that ferritin binding sites were present on cells expressing the proliferation markers HLA-DR, MLR3, interleukin 2 (IL- 2), and transferrin receptors (Tf-R). In addition, after PHA induction, the time course of the expression of H-ferritin binding sites was similar to those of the above proliferation markers. Ferritin binding sites were observed in lymphocytes at all cell cycle phases, including the early S-phase. H-Ferritin at nanomolar and picomolar concentrations had an inhibitory effect on PHA-induced blastogenesis. We propose that H-ferritin binding sites behave like proliferation markers, with the unusual function of downregulating proliferation.


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