Chandrasekera P et al. (2022), Metalloprotease ADAM9 cleaves ephrin-B ligands ...

XB-ART-59191

J Biol Chem 2022 Aug 01;2988:102225. doi: 10.1016/j.jbc.2022.102225.

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Metalloprotease ADAM9 cleaves ephrin-B ligands and differentially regulates Wnt and mTOR signaling downstream of Akt kinase in colorectal cancer cells.

Chandrasekera P , Perfetto M , Lu C , Zhuo M , Bahudhanapati H , Li J , Chen WC , Kulkarni P , Christian L , Liu J , Yien YY , Yu C , Wei S .

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Ephrin-B signaling has been implicated in many normal and pathological processes, including neural crest development and tumor metastasis. We showed previously that proteolysis of ephrin-B ligands by the disintegrin metalloprotease ADAM13 is necessary for canonical Wnt signal activation and neural crest induction in Xenopus, but it was unclear if these mechanisms are conserved in mammals. Here, we report that mammalian ADAM9 cleaves ephrin-B1 and ephrin-B2 and can substitute for Xenopus ADAM13 to induce the neural crest. We found that ADAM9 expression is elevated in human colorectal cancer (CRC) tissues and that knockdown (KD) of ADAM9 inhibits the migration and invasion of SW620 and HCT116 CRC cells by reducing the activity of Akt kinase, which is antagonized by ephrin-Bs. Akt is a signaling node that activates multiple downstream pathways, including the Wnt and mTOR pathways, both of which can promote CRC cell migration/invasion. Surprisingly, we also found that KD of ADAM9 downregulates Wnt signaling but has negligible effects on mTOR signaling in SW620 cells; in contrast, mTOR activity is suppressed while Wnt signaling remains unaffected by ADAM9 KD in HCT116 cells. These results suggest that mammalian ADAM9 cleaves ephrin-Bs to derepress Akt and promote CRC migration and invasion; however, the signaling pathways downstream of Akt are differentially regulated by ADAM9 in different CRC cell lines, reflecting the heterogeneity of CRC cells in responding to manipulations of upstream Akt regulators.

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Genes referenced: adam13 adam28.2 adam9 calr ephb3 mtor myc ptpa rps6kb1 snai2
GO keywords: ephrin receptor activity [+]
???displayArticle.antibodies??? Adam9 Ab1 Akt1 Ab10 Ctnnb1 Ab21 Ctnnb1 Ab22 HA Ab30 Myc Ab16 Rps6kb1 Ab1 Rps6kb1 Ab2

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	Figure 1. ADAM9 cleaves ephrin-B1 and -B2 and can substitute for Xenopus ADAM13 in neural crest induction. A and B, HEK293T cells were transfected with plasmids encoding N-terminally HA-tagged ephrin-B1 (A) or -B2 (B) and C-terminally myc-tagged WT ADAM9 or the E348A mutant, and Western blotting was carried out using the indicated antibodies. Arrowheads point to the shed ectodomain of ephrin-Bs. C and D, HCT116 cells were transfected with the indicated siRNA, and RT-qPCR (C) and Western blotting (D) were carried out for ADAM9 mRNA and protein, respectively. Unpaired t tests were performed for log2FC of mRNA levels obtained for three biological replicates in (C), and error bars represent SEM. E-G, HCT116 (E and G) or SW620 (F) cells were transfected with the indicated siRNA and plasmid, and Western blotting was carried out using an anti-HA (E and F) or phospho-EphB3 (G) antibody. H, two-cell stage Xenopus tropicalis embryos were injected in one blastomere with the indicated MO and mRNA, allowed to develop to stage âˆ¼12.5, and processed for in situ hybridization for snai2. Ï‡2 test was performed for the percentage of normal embryos (n indicates total number of embryos examined). Red asterisks denote the injected side, and arrow indicates the expansion of snai2 expression domain. The scale bar represents 250 Î¼m. CL, cell lysates; CM, conditioned media; CT, control; FC, fold change; M, mature form; P, pro-form (same below). ADAM, A Disintegrin and Metalloprotease; RT-qPCR, quantitative RT-PCR; MO, morpholino.
	Figure 2. ADAM9 mRNA is upregulated in human CRC samples and promotes CRC cell migration and invasion in vitro. A, comparison of ADAM9 transcripts in CRC tissues (T) with matched adjacent normal tissues (N) from individual patients, as measured by RT-qPCR analyses (left). Results of 48 samples are summarized on the right, and Wilcoxon matched-pairs signed rank test was performed. B and C, SW620 or HCT116 cells were transfected with the indicated siRNA, and transwell migration (B) and invasion (C) assays were carried out as described in Experimental procedures. Results of three biological replicates for each treatment are summarized on the right, and unpaired t test was performed. Error bars represent SD. The scale bars represent 100 Î¼m. ADAM, A Disintegrin and Metalloprotease; CRC, colorectal cancer; RT-qPCR, quantitative RT-PCR.
	Figure 3. KD of ADAM9 inhibits Wnt activity in HEK293T and SW620 but not HCT116 cells. Cells were transfected with the indicated siRNA and plasmid. A-C, TOP/FOPFLASH luciferase reporter assays were carried out in triplicate with the indicated cell lines, and unpaired t tests were performed to compare Wnt activity. Error bars represent SD. D and E, Western blotting was carried out for cell lysates with the antibodies for total and active Î²-catenin, as indicated, in SW620 (D) or HCT116 (E) cells. Western blotting was repeated in triplicate to confirm the effects of ADAM9 KD on active Î²-catenin (see Fig. S3 for images of blots); unpaired t tests were performed for log2FC of protein levels and summarized in graphs (error bars represent SEM). ADAM, A Disintegrin and Metalloprotease; KD, knockdown.
	Figure 4. KD of ADAM9 inhibits Akt activity but differentially affects mTOR signaling in HCT116 and SW620 cells. A-C, HCT116 cells were transfected with control or AD9-1 siRNA, and RT-qPCR was carried out for the indicated genes in three biological replicates. D and E, Western blotting was carried out for cell lysates with the antibodies for the indicated proteins in HCT116 (D) or SW620 (E) cells transfected with control or AD9-1 siRNA. Western blotting was repeated in triplicate to confirm the effects of ADAM9 KD on phospho-S6K and phosphor-Ser473 Akt (see Fig. S4 for images of blots); unpaired t tests were performed for log2FC of protein levels and summarized in graphs (error bars represent SEM). ADAM, A Disintegrin and Metalloprotease; KD, knockdown; RT-qPCR, quantitative RT-PCR.
	Figure 5. ADAM9 activates Akt, possibly via the ephrin-Bâ€“PP2A axis, to promote CRC cell migration and invasion. A-D, SW620 cells were transfected with the indicated siRNA and plasmid, and transwell migration (A and C) and invasion (B and D) assays were performed in triplicate. E, HCT116 cells were transfected with empty vector or a plasmid encoding HA-tagged ephrin-B1Î”C, and Western blotting was carried out using the indicated antibodies (anti-HA for ephrin-B1Î”C). F, HEK293T cells were transfected with the indicated plasmids and treated with 1 Î¼M okadaic acid, and TOP/FOPFLASH assays were carried out for cell lysates obtained for three biological replicates. G, a model for ADAM9 function in CRC migration and invasion. Unpaired t tests were performed in A-D and F; error bars represent SD. The scale bars represent 100 Î¼m. ADAM, A Disintegrin and Metalloprotease; CRC, colorectal cancer; PP2A, protein phosphatase 2A.
	Figure S1 Transfection of HCT116 cells with siAD9-2 inhibits ephrin-B1 shedding. HCT116 cells were transfected with a plasmid encoding N-terminally HA-tagged ephrin-B1 with siControl (CT) or siAD9-2, and western blotting was carried out for conditioned media (CM) or cell lysates (CL) using an anti-HA antibody.
	Figure S2 Transfection of SW620 and HCT116 cells with siAD9-2 inhibits migration and invasion. SW620 or HCT116 cells were transfected with the indicated siRNA, and transwell migration (A) and invasion (B) assays were carried out as described in Experimental procedures. Results of 3 biological replicates for each treatment are summarized on the right, and unpaired t test was performed. Error bars represent standard deviation. Scale bars, 100 Î¼m.
	Figure S3 KD of ADAM9 reduces active b-catenin in SW620 but not HCT116 cells. SW620 (A) and HCT116 (B) cells were transfected with the indicated siRNA, and western blotting was performed for cell lysates using the indicated antibodies. Experiments were carried out in triplicate, and statistics are presented in Fig. 3D and E, respectively.
	Figure S4 Effects of ADAM9 KD on phospho-S6K and phospho-Ser473 Akt in HCT116 and SW620 cells. HCT116 (A and B) and SW620 (C and D) cells were transfected with the indicated siRNA, and western blotting was performed for cell lysates using the indicated antibodies. Experiments were carried out in triplicate, and statistics are presented in Fig. 4D and E, respectively.
	Figure S5 Transfection of HCT116 cells with either siAD9-1 or siAD9-2 inhibits Akt activity. HCT116 cells were transfected with the indicated siRNA, and western blotting was carried out for cell lysates using the indicated antibodies.
	Figure S6 Overexpression of ADAM9 in HCT116 cells leads to increased migration and invasion, which can be blocked by Akt inhibition. HCT116 cells were transfected with empty pCS2+ vector (Mock) or pCS2+:Adam9, and treated with DMSO (vehicle control) or 12.5 nM of the selective Akt inhibitor MK-2206. Transwell migration (A) and invasion (B) assays were carried out. Results of 3 biological replicates for each treatment are summarized on the right, and unpaired t test was performed. Error bars represent standard deviation. Scale bars, 100 Î¼m.
	Figure S7 The ephrin-B1 siRNAs effectively reduce ephrin-B1 mRNA in SW620 cells. SW620 cells were transfected with the indicated siRNAs, and RT-qPCR was carried out for ephrin-B1 mRNA. Unpaired t tests were performed for log2FC of mRNA levels obtained for 3 biological replicates, and error bars represent standard error of the mean (SEM).
	Figure S8 Overexpression of ephrin-B1DC in SW620 cells inhibits Akt activity. SW620 cells were transfected with an empty vector or a plasmid encoding HA-tagged ephrin-B1DC, and western blotting was carried out for cell lysates using the indicated antibodies (anti-HA for ephrin-B1DC).
	Figure S9 Overexpression of EphB1DK in SW620 cells enhances Akt and Wnt activities. SW620 cells were transfected with an empty vector or a plasmid encoding HA-tagged EphB1DK, and western blotting (A) or TOP/FOPFLASH luciferase activity assay (B) was carried out for cell lysates. Cells transfected with a plasmid encoding caAkt were used as a positive control in A. Unpaired t test was performed to compare Wnt activity in B, and error bars represent standard deviation.

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Ahmed, Epigenetic and genetic features of 24 colon cancer cell lines. 2013, Pubmed