Description

The Sting1 Knockout LL/2 (LLC1) Cell Line is a CRISPR/Cas9-edited knockout cell line derived from the mouse Lewis lung carcinoma LL/2 (LLC1) parental line. This product features targeted disruption of the Sting1 gene, generating a loss-of-function model for STING-dependent innate immune signaling. As a stable knockout cell line, it provides a consistent background for interrogating STING??s role in cancer biology, immune recognition, and therapeutic response. This engineered cell line enables robust, reproducible dissection of STING-mediated pathways in vitro and in syngeneic tumor models.

The LL/2 (LLC1) host cell line was established from a spontaneous lung carcinoma in a C57BL/6 mouse and is a widely used syngeneic model for non?small cell lung cancer (NSCLC). These adherent cells are highly tumorigenic and metastatic, ideal for studying tumor progression, metastasis, and the tumor?Cimmune interface. The immunocompetent background allows evaluation of immune?mediated tumor control following implantation. LL/2 cells are well-characterized for their response to immunomodulatory agents, including STING agonists, and form tumors with a microenvironment resembling human NSCLC.

STING (stimulator of interferon genes), encoded by Sting1, is an ER?resident adaptor central to cytosolic DNA sensing. The enzyme cGAS generates 2??3???cGAMP upon DNA detection, activating STING. Activated STING translocates to the Golgi, recruiting and activating TBK1, which phosphorylates IRF3, driving nuclear translocation and induction of type I interferons and ISGs such as Ifit1, Cxcl10, and Isg15. STING also signals to NF???B, upregulating pro?inflammatory cytokines including IL?6 and TNF???. Regulatory factors like TRIM56, RNF5, and PPP6C modulate STING activity.

Knockout of Sting1 in the LL/2 (LLC1) background abrogates STING-dependent innate immune signaling, rendering cells unresponsive to cytosolic DNA and STING agonists such as DMXAA or c?di?AMP. Consequently, downstream activation of TBK1, IRF3, and NF???B is disrupted, eliminating type I interferon and ISG induction. In vivo, Sting1?deficient tumors are expected to show altered immune cell infiltration, reduced dendritic cell activation, and impaired CD8+ T cell priming, fostering an immunosuppressive microenvironment. This line serves as a critical control for dissecting cancer cell?intrinsic STING signaling in NSCLC.

Researchers can employ this cell line in RT?qPCR for ISG expression, western blotting for phospho?TBK1 and phospho?IRF3, and ELISA for IFN??? secretion. Flow cytometry profiles tumor?infiltrating immune populations, while cytokine multiplex assays quantify secretome changes. Syngeneic tumor growth studies in C57BL/6 mice assess STING agonist efficacy, checkpoint inhibitor combinations, and the role of tumor STING in anti?tumor immunity. Immunofluorescence can track STING trafficking in wild?type controls. For further details, please contact Ascent Research.