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Biophysical changes reduce energetic demand in growth factor-deprived lymphocytes

Authors
Hecht, Vivian C.Sullivan, Lucas B.Kimmerling, Robert J.Kim, Dong-HweeHosios, Aaron M.Stockslager, Max A.Stevens, Mark M.Kang, Joon HoWirtz, DenisVander Heiden, Matthew G.Manalis, Scott R.
Issue Date
15-Feb-2016
Publisher
ROCKEFELLER UNIV PRESS
Citation
JOURNAL OF CELL BIOLOGY, v.212, no.4, pp.439 - 447
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CELL BIOLOGY
Volume
212
Number
4
Start Page
439
End Page
447
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/89518
DOI
10.1083/jcb.201506118
ISSN
0021-9525
Abstract
Cytokine regulation of lymphocyte growth and proliferation is essential for matching nutrient consumption with cell state. Here, we examine how cellular biophysical changes that occur immediately after growth factor depletion promote adaptation to reduced nutrient uptake. After growth factor withdrawal, nutrient uptake decreases, leading to apoptosis. Bcl-xL expression prevents cell death, with autophagy facilitating long-term cell survival. However, autophagy induction is slow relative to the reduction of nutrient uptake, suggesting that cells must engage additional adaptive mechanisms to respond initially to growth factor depletion. We describe an acute biophysical response to growth factor withdrawal, characterized by a simultaneous decrease in cell volume and increase in cell density, which occurs before autophagy initiation and is observed in both FL5.12 Bcl-xL cells depleted of IL-3 and primary CD8(+) T cells depleted of IL-2 that are differentiating toward memory cells. The response reduces cell surface area to minimize energy expenditure while conserving biomass, suggesting that the biophysical properties of cells can be regulated to promote survival under conditions of nutrient stress.
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