Identification of senescent cell surface targetable protein DPP4

Kyoung Mi Kim(National Institutes of Health), Ji Heon Noh(National Institutes of Health), Monica Bodogai(National Institutes of Health), Jennifer L. Martindale(National Institutes of Health), Xiaoling Yang(National Institutes of Health), Fred E. Indig(National Institutes of Health), Sandip K. Basu(National Institutes of Health), Kei Ohnuma(Juntendo University), Chikao Morimoto(Juntendo University), Peter F. Johnson(National Institutes of Health), Arya Biragyn(National Institutes of Health), Kotb Abdelmohsen(National Institutes of Health), Myriam Gorospe(National Institutes of Health)
Genes & Development
August 1, 2017
Cited by 255Open Access
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Abstract

Senescent cell accumulation in aging tissues is linked to age-associated diseases and declining function, prompting efforts to eliminate them. Mass spectrometry analysis revealed that DPP4 (dipeptidyl peptidase 4) was selectively expressed on the surface of senescent, but not proliferating, human diploid fibroblasts. Importantly, the differential presence of DPP4 allowed flow cytometry-mediated isolation of senescent cells using anti-DPP4 antibodies. Moreover, antibody-dependent cell-mediated cytotoxicity (ADCC) assays revealed that the cell surface DPP4 preferentially sensitized senescent, but not dividing, fibroblasts to cytotoxicity by natural killer cells. In sum, the selective expression of DPP4 on the surface of senescent cells enables their preferential elimination.


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