“Suppressor factor” of neutrophils: A short story of a long-term misconception


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Abstract

A large body of evidence obtained during the last decade has demonstrated that neutrophils suppress T cell proliferation in different models of inflammation and cell interaction. The commonly used method for assessing cell proliferation and proliferation inhibition is measuring [3H]thymidine incorporation into cells. Earlier, we observed inhibition of [3H]thymidine uptake in experiments on neutrophil-mediated regulation of T cell response in tuberculosis immunity. Here, we used different types of proliferating cells to analyze the nature of the soluble “neutrophil factor” by a variety of methods (dialysis, HPLC, mass spectrometry, and NMR) and unambiguously demonstrated that neutrophils do not synthesize a specific factor inhibiting cell proliferation, but secrete high concentrations of extracellular thymidine that competitively inhibit [3H]thymidine incorporation. Although the physiological significance of thymidine secretion by neutrophils remains unknown, this phenomenon should be carefully considered when designing test systems for studying cell–cell interactions.

About the authors

I. A. Linge

Central Research Institute for Tuberculosis

Author for correspondence.
Email: iralinge@gmail.com
Russian Federation, Moscow, 107564

E. V. Kondratieva

Central Research Institute for Tuberculosis

Email: asapt@aha.ru
Russian Federation, Moscow, 107564

T. K. Kondratieva

Central Research Institute for Tuberculosis

Email: asapt@aha.ru
Russian Federation, Moscow, 107564

V. A. Makarov

Institute of Molecular Medicine

Email: asapt@aha.ru
Russian Federation, Moscow, 119991

V. I. Polshakov

Faculty of Fundamental Medicine, Center for Magnetic Tomography and Spectroscopy

Email: asapt@aha.ru
Russian Federation, Moscow, 119991

O. Yu. Savelyev

Faculty of Fundamental Medicine, Center for Magnetic Tomography and Spectroscopy

Email: asapt@aha.ru
Russian Federation, Moscow, 119991

A. S. Apt

Central Research Institute for Tuberculosis

Author for correspondence.
Email: asapt@aha.ru
Russian Federation, Moscow, 107564


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