Figure 3.
MyD88 is dispensable for MDS/AML LSPCs. (A) Immunoblots for MyD88 and the activation of downstream pathways (phospho-p38, phospho-JNK, phospho-IKK, and phospho- extracellular signal-regulated kinase) in WT and MYD88KO THP1 cells upon a 30-minute treatment with IL-1β (10 ng/µL) or the TLR1/2 ligand PAM3CSK4 (1 µg/mL) as compared with DMSO. (B) Immunoblots for IRAK4 and MyD88 in WT and MYD88KO THP1 and MDSL cells transduced with nontargeting shControl or shIRAK4. (C) Colony formation of WT and MYD88KO THP1 and MDSL cells transduced with nontargeting shControl or shIRAK4. (D) Representative colony images of WT and MyD88KO MDSL cells transduced with nontargeting shControl or shIRAK4 (original magnification ×40). Significance was determined with a Student t test (∗P < .05). Error bars represent the standard deviation. DMSO, dimethyl sulfoxide.

MyD88 is dispensable for MDS/AML LSPCs. (A) Immunoblots for MyD88 and the activation of downstream pathways (phospho-p38, phospho-JNK, phospho-IKK, and phospho- extracellular signal-regulated kinase) in WT and MYD88KO THP1 cells upon a 30-minute treatment with IL-1β (10 ng/µL) or the TLR1/2 ligand PAM3CSK4 (1 µg/mL) as compared with DMSO. (B) Immunoblots for IRAK4 and MyD88 in WT and MYD88KO THP1 and MDSL cells transduced with nontargeting shControl or shIRAK4. (C) Colony formation of WT and MYD88KO THP1 and MDSL cells transduced with nontargeting shControl or shIRAK4. (D) Representative colony images of WT and MyD88KO MDSL cells transduced with nontargeting shControl or shIRAK4 (original magnification ×40). Significance was determined with a Student t test (∗P < .05). Error bars represent the standard deviation. DMSO, dimethyl sulfoxide.

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