The role of nutrients in B lymphocyte growth and survival responses

• Published in: The Journal of immunology (1950) Vol. 196; no. 1_Supplement; pp. 204 - 204.16
• Main Authors: Heyse, Shannon A, Connolly, Timothy, Chiles, Thomas Crane
• Format: Journal Article
• Language: English
• Published: 01.05.2016
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.196.Supp.204.16

Abstract B cell activation is an energetically demanding process during which B lymphocytes shift from a resting state to a proliferative, metabolically active state. Little is known about the metabolic reprogramming process or the role extracellular nutrients play in the activation response. We demonstrate that there are distinct requirements for the nutrients L-glutamine and glucose during activation. We show that cells activated in glucose-depleted conditions are still able to undergo growth and signaling events. In contrast, we show that extracellular L-glutamine is essential for all but the earliest activation events, and cells cultured in L-glutamine-deprived conditions are unable to enter the cell cycle. Consistently, we show that extracellular supplementation of the cell-permeable derivative of a-ketoglutarate (a-KG) is able to rescue cell activation in the absence of glutamine. We also show the induction of the high affinity amino acid transporter ASCT2 is required for glutamine uptake following BCR crosslinking. Specifically, we found that halting glutamine uptake or processing by inhibiting ASCT2 or the glutaminolytic enzyme glutaminase causes activation defects that parallel those observed in glutamine deprived conditions, indicating a requirement for glutaminolysis during the very early stages of activation. Finally, we found that a-KG does not contribute to epigenetic remodeling, but is necessary for mTORC1 activation. In turn, mTORC1 activity is required for upregulation of the glucose transporter Glut1 during activation, as well as increased glucose uptake. These findings indicate a distinct metabolic profile that begins with glutamine uptake, and acts through mTORC1 signaling to later promote glucose uptake.