Natural killer function in flow cytometry. III. Surface marker determination of K562-conjugated lymphocytes by dual laser flow cytometry

Marco Vitale, Loris Zamai, Stefano Papa, Giovanni Mazzotti, Andrea Facchini, Giuseppe Monti, Francesco Antonio Manzoli

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The recognition of effector cell populations that are able to actively form conjugates with target cells is of major importance in studies of lymphocyte cytotoxicity. A number of methodologies have been described to identify the conjugates and count them, but there have been few studies of the birding capability of the different subsets of effector cells involved in the conjugation phenomenon. Here we describe a methodology that permits the study of two surface markers on lymphocytes conjugated to K562 target cells. In particular, the expression of low density CD8 (CD8dim) has been studied on both CD3+ and CD16+ lymphocytes bound to K562 target cells. Previously described methodologies, either optical microscopy or flow cytometry, were not able to identify the effector population by mAb double staining, especially in the case of antigens expressed at low density. The flow cytometric methodology described here permits the measurement of the binding activity of small lymphocyte subsets such as the CD3+8dim+ population. However, the method could be used to study the binding activity of any effector population defined by mAb double staining.

Original languageEnglish
Pages (from-to)189-196
Number of pages8
JournalJournal of Immunological Methods
Volume149
Issue number2
DOIs
Publication statusPublished - 1992

Fingerprint

Flow Cytometry
Lasers
Lymphocytes
K562 Cells
Population
Staining and Labeling
Lymphocyte Subsets
Microscopy
Antigens

Keywords

  • Binding
  • CD8
  • CD8
  • Conjugate
  • Dual laser flow cytometry
  • K562

ASJC Scopus subject areas

  • Biotechnology
  • Immunology

Cite this

Natural killer function in flow cytometry. III. Surface marker determination of K562-conjugated lymphocytes by dual laser flow cytometry. / Vitale, Marco; Zamai, Loris; Papa, Stefano; Mazzotti, Giovanni; Facchini, Andrea; Monti, Giuseppe; Manzoli, Francesco Antonio.

In: Journal of Immunological Methods, Vol. 149, No. 2, 1992, p. 189-196.

Research output: Contribution to journalArticle

Vitale, Marco ; Zamai, Loris ; Papa, Stefano ; Mazzotti, Giovanni ; Facchini, Andrea ; Monti, Giuseppe ; Manzoli, Francesco Antonio. / Natural killer function in flow cytometry. III. Surface marker determination of K562-conjugated lymphocytes by dual laser flow cytometry. In: Journal of Immunological Methods. 1992 ; Vol. 149, No. 2. pp. 189-196.
@article{55975c26646149c785c2edd5257f7ba3,
title = "Natural killer function in flow cytometry. III. Surface marker determination of K562-conjugated lymphocytes by dual laser flow cytometry",
abstract = "The recognition of effector cell populations that are able to actively form conjugates with target cells is of major importance in studies of lymphocyte cytotoxicity. A number of methodologies have been described to identify the conjugates and count them, but there have been few studies of the birding capability of the different subsets of effector cells involved in the conjugation phenomenon. Here we describe a methodology that permits the study of two surface markers on lymphocytes conjugated to K562 target cells. In particular, the expression of low density CD8 (CD8dim) has been studied on both CD3+ and CD16+ lymphocytes bound to K562 target cells. Previously described methodologies, either optical microscopy or flow cytometry, were not able to identify the effector population by mAb double staining, especially in the case of antigens expressed at low density. The flow cytometric methodology described here permits the measurement of the binding activity of small lymphocyte subsets such as the CD3+8dim+ population. However, the method could be used to study the binding activity of any effector population defined by mAb double staining.",
keywords = "Binding, CD8, CD8, Conjugate, Dual laser flow cytometry, K562",
author = "Marco Vitale and Loris Zamai and Stefano Papa and Giovanni Mazzotti and Andrea Facchini and Giuseppe Monti and Manzoli, {Francesco Antonio}",
year = "1992",
doi = "10.1016/0022-1759(92)90250-W",
language = "English",
volume = "149",
pages = "189--196",
journal = "Journal of Immunological Methods",
issn = "0022-1759",
publisher = "Elsevier",
number = "2",

}

TY - JOUR

T1 - Natural killer function in flow cytometry. III. Surface marker determination of K562-conjugated lymphocytes by dual laser flow cytometry

AU - Vitale, Marco

AU - Zamai, Loris

AU - Papa, Stefano

AU - Mazzotti, Giovanni

AU - Facchini, Andrea

AU - Monti, Giuseppe

AU - Manzoli, Francesco Antonio

PY - 1992

Y1 - 1992

N2 - The recognition of effector cell populations that are able to actively form conjugates with target cells is of major importance in studies of lymphocyte cytotoxicity. A number of methodologies have been described to identify the conjugates and count them, but there have been few studies of the birding capability of the different subsets of effector cells involved in the conjugation phenomenon. Here we describe a methodology that permits the study of two surface markers on lymphocytes conjugated to K562 target cells. In particular, the expression of low density CD8 (CD8dim) has been studied on both CD3+ and CD16+ lymphocytes bound to K562 target cells. Previously described methodologies, either optical microscopy or flow cytometry, were not able to identify the effector population by mAb double staining, especially in the case of antigens expressed at low density. The flow cytometric methodology described here permits the measurement of the binding activity of small lymphocyte subsets such as the CD3+8dim+ population. However, the method could be used to study the binding activity of any effector population defined by mAb double staining.

AB - The recognition of effector cell populations that are able to actively form conjugates with target cells is of major importance in studies of lymphocyte cytotoxicity. A number of methodologies have been described to identify the conjugates and count them, but there have been few studies of the birding capability of the different subsets of effector cells involved in the conjugation phenomenon. Here we describe a methodology that permits the study of two surface markers on lymphocytes conjugated to K562 target cells. In particular, the expression of low density CD8 (CD8dim) has been studied on both CD3+ and CD16+ lymphocytes bound to K562 target cells. Previously described methodologies, either optical microscopy or flow cytometry, were not able to identify the effector population by mAb double staining, especially in the case of antigens expressed at low density. The flow cytometric methodology described here permits the measurement of the binding activity of small lymphocyte subsets such as the CD3+8dim+ population. However, the method could be used to study the binding activity of any effector population defined by mAb double staining.

KW - Binding

KW - CD8

KW - CD8

KW - Conjugate

KW - Dual laser flow cytometry

KW - K562

UR - http://www.scopus.com/inward/record.url?scp=0026581631&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0026581631&partnerID=8YFLogxK

U2 - 10.1016/0022-1759(92)90250-W

DO - 10.1016/0022-1759(92)90250-W

M3 - Article

VL - 149

SP - 189

EP - 196

JO - Journal of Immunological Methods

JF - Journal of Immunological Methods

SN - 0022-1759

IS - 2

ER -