TY - JOUR
T1 - Biophysical changes reduce energetic demand in growth factor-deprived lymphocytes
AU - Hecht, Vivian C.
AU - Sullivan, Lucas B.
AU - Kimmerling, Robert J.
AU - Kim, Dong Hwee
AU - Hosios, Aaron M.
AU - Stockslager, Max A.
AU - Stevens, Mark M.
AU - Kang, Joon Ho
AU - Wirtz, Denis
AU - Vander Heiden, Matthew G.
AU - Manalis, Scott R.
N1 - Funding Information:
This work was supported by a Koch Institute Support (core) grant from the National Cancer Institute (P30-CA14051), Physical Sciences Oncology Center (U54CA143874), Burrough''s Wellcome Foundation, the Ludwig Center at the Massachusetts Institute of Technology, and the Damon Runyon Cancer Research Foundation. Lucas B. Sullivan was supported by a postdoctoral fellowship from the American Cancer Society (PF-15-096-01-TBE).
Publisher Copyright:
© 2016 Newell-Litwa.
PY - 2016
Y1 - 2016
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84959575526&partnerID=8YFLogxK
U2 - 10.1083/jcb.201506118
DO - 10.1083/jcb.201506118
M3 - Article
C2 - 26880201
AN - SCOPUS:84959575526
SN - 0021-9525
VL - 212
SP - 439
EP - 447
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 4
ER -