Asymmetric cell division safeguards memory CD8 T cell development

Graebnitz, F.; Stark, D.; Shlesinger, D.; Petkidis, A.; Borsa, M.; Yermanos, A.; Carr, A.; Barandun, N.; Wehling, A.; Balaz, M.; Schroeder, T.; Oxenius, A.

doi:10.1101/2022.11.08.515624

bioRxiv · 10.1101/2022.11.08.515624

Asymmetric cell division safeguards memory CD8 T cell development

Graebnitz, F.·Stark, D.·Shlesinger, D.·Petkidis, A.·Borsa, M.·Yermanos, A.·Carr, A.·Barandun, N.·Wehling, A.·Balaz, M.·Schroeder, T.·Oxenius, A.

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Abstract

The strength of T cell receptor (TCR) stimulation and asymmetric distribution of fate determinants are both implied to affect T cell differentiation. Here, we uncovered asymmetric cell division (ACD) as a safeguard mechanism for memory CD8 T cell generation specifically upon strong TCR stimulation. Using live imaging approaches, we found that strong TCR stimulation induced elevated ACD rates and subsequent single cell derived colonies comprised both effector and memory precursor cells. The abundance of memory precursor cells emerging from a single activated T cell positively correlated with first mitosis ACD. Accordingly, preventing ACD by inhibition of PKC{zeta} during the first mitosis upon strong TCR stimulation markedly curtailed the formation of memory precursor cells. Conversely, no effect of ACD on fate commitment was observed upon weak TCR stimulation. Our data provide new mechanistic insights into the role of ACD for CD8 T cell fate regulation upon different activation conditions.

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Graebnitz, F., Stark, D., Shlesinger, D., Petkidis, A., Borsa, M., Yermanos, A., Carr, A., Barandun, N., Wehling, A., Balaz, M., Schroeder, T., Oxenius, A.. 2022-11-09. Asymmetric cell division safeguards memory CD8 T cell development. https://doi.org/10.1101/2022.11.08.515624

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