Activation-induced thrombospondin-4 works with thrombospondin-1 to build cytotoxic supramolecular attack particles.

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Tác giả: Nadia Alawar, Cosima T Baldari, Ute Becherer, Bruce R Blazar, Nagaja Capitani, Chiara Cassioli, Hsin-Fang Chang, Ewoud B Compeer, Michael L Dustin, Francesca Finetti, Ludovica Lopresti, Giuseppe Marotta, Annachiara Miccoli, Jemma Nicholls, Anna Onnis, Laura Patrussi, Claudia Schirra, Claire C Staton, Carmela Tangredi, Vanessa Tatangelo, Livio Trentin, Szu-Min Tu, Salvatore Valvo, Matthew J A Wood

Ngôn ngữ: eng

Ký hiệu phân loại: 338.54 Economic fluctuations

Thông tin xuất bản: United States : Proceedings of the National Academy of Sciences of the United States of America , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 178310

 Cytotoxic attack particles released by CTLs and NK cells include diverse phospholipid membrane and glycoprotein encapsulated entities that contribute to target cell killing. Supramolecular attack particles (SMAPs) are one type of particle characterized by a cytotoxic core enriched in granzymes and perforin surrounded by a proteinaceous shell including thrombospondin (TSP)-1. TSP-4 was also detected in bulk analysis of SMAPs released by CTLs
  however, it has not been investigated whether TSP-4 contributes to distinct SMAP types or the same SMAP type as TSP-1 and, if in the same type of SMAP, whether TSP-4 and TSP-1 cooperate or compete. Here, we observed that TSP-4 expression increased upon CD8
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