Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2019 Nov 22;9:17369. doi: 10.1038/s41598-019-53910-y

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

CDK9 inhibition reduced necroptotic cell death. (A) THP-1 cells were pretreated with FVD to inhibit CDK9 for 2 hours, and then stimulated with P. gingivalis. Expression of lactate dehydrogenase in the cell supernatants were assessed by LDH assay at 4- and 8-hours post-infection to represent cell death. (B) Same treatment was performed on PBMCs, and the expression of lactate dehydrogenase were detected. (C) The RNA levels of THP-1 cells related to necroptosis including TRIF, cFLIP_S, cFLIP_L, caspase-8, RIPK1, RIPK3 and MLKL were detected by real-time PCR. (D) The translational level was further detected by western blot. The images were collected from different gels with the same amount of samples. (**p < 0.01; ***p < 0.001).