Abstract

Cell growth is driven by the acquisition and synthesis of both dry biomass and water mass. In this study, we examine the increase of water mass in T cell during cell growth. We found that T-cell growth is characterized by an initial phase of slow increase in cellular water, followed by a second phase of rapid increase in water content. To study the origin of the water gain, we developed a novel methodology we call cold aqua trap-isotope ratio mass spectrometry, which allows analysis of the isotope composition of intracellular water. Applying cold aqua trap-isotope ratio mass spectrometry, we discovered that glycolysis-coupled metabolism of water accounts on average for 11 fl out of the 20 fl of water gained per cell during the initial slow phase. In addition, we show that at the end of the rapid phase before initiation of cell division, a water influx occurs, increasing the cellular water mass by threefold. Thus, we conclude that activated T cells switch from metabolizing water to rapidly taking up water from the extracellular medium prior to cell division. Our work provides a method to analyze cell water content as well as insights into the ways cells regulate their water mass.

Highlights

  • Cell growth requires cells to accumulate mass and to increase in physical size as a prerequisite step in development and proliferation [1, 2]

  • Analysis of cellular water dynamics during T cell activation growth phases, we developed a novel method based on the intracellular water isotope composition, called cold aqua trapisotope ratio mass spectrometry (CAT-IRMS)

  • Stimulation of primary T cells leads to the initiation of a tightly coordinated and well-defined cell growth program leading to a significant increase in cell size [15, 16]

Read more

Summary

Introduction

Cell growth requires cells to accumulate mass and to increase in physical size as a prerequisite step in development and proliferation [1, 2]. Analysis of cellular water dynamics during T cell activation growth phases, we developed a novel method based on the intracellular water isotope composition, called cold aqua trapisotope ratio mass spectrometry (CAT-IRMS). In the first slow-growth phase, the initial 12 h following stimuli, average volume per T cell increased from 174.3 to 228.3 fl, at a rate of 4.4 fl/h.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call