TRIM3 Negatively Regulates Autophagy Through Promoting Degradation of Beclin1 in Ewing Sarcoma Cells.

BACKGROUND AND AIM: Ewing sarcoma (ES) is an aggressive neoplasm predominantly occurring in adolescents and has a poor prognosis when metastasized. In the current study, we were aiming to investigate the function of TRIM3 in autophagy in ES cells.
METHODS: The expression of TRIM3 in Ewing sarcoma tissues and normal tissues was examined by quantitative PCR and western blot. The effect of TRIM3 on autophagy was detected by western blot and immunofluorescence assay. Target of TRIM3 was examined by western blot, immunoprecipitation and ubiquitination assay.
RESULTS: We found the expression of TRIM3 was significantly up-regulated in Ewing sarcoma tissues compared with normal tissues, and this phenomenon was regulated by EWS-FLI1 expression. Furthermore, we observed that overexpression of TRIM3 markedly and consistently inhibited autophagy in ES cells, and autophagy was enhanced in TRIM3-silenced ES cells. Finally, we found in ES cells, TRIM3 could directly interact with Beclin1, and improved its K48-linked polyubiquitinaion, leading to the degradation of Beclin1 and then regulated autophagy.
CONCLUSION: In the present research, for the first time we revealed that TRIM3 negatively regulates autophagy through promoting degradation of Beclin1 in Ewing sarcoma cells, and these findings may provide ideas for ES research.

Introduction

ES is an aggressive bone and soft tissue malignancy, which mainly affects children and young people.1 In recent years, with the development of multidrug systemic chemotherapy and active local control measures, the overall survival rate of patients with local diseases has been significantly improved.2 However, for the ~25% of patients who present with metastatic disease, the prognosis is poor and event-free survival rate for these patients remains <25%.3 Thus, it is of great significance to develop new novel therapeutic targets for the treatment of ES.

Autophagy is a eukaryotic homeostatic mechanism whereby cells remove from their cytoplasm toxic aggregates, damaged and surplus organelles, invading pathogens or utilize bulk cytosol for and metabolic needs.4 Abnormal autophagy has also been implicated in pathological development, emphasizing its critical involvement in maintaining homeostasis at the cellular and organismic level.5 Beclin1 (BECN1) is a B-cell lymphoma 2 (Bcl-2) homology 3 domain-only protein, it is a central protein that assembles cofactors for the formation of a BECN1-PIK3C3-PIK3R4 complex to trigger the autophagy protein cascade which are utilized in the initiation of autophagy.6 However, the effect of Beclin1 and its regulation in ES still remain largely unknown.

TRIM proteins share a similar characteristic structure, which includes a RING (R) domain, one or two B-boxes (B), and a coiled coil (CC) domain in the N-terminal and a domain in the C-terminal with variable structures.7,8 TRIM proteins are involved in a broad range of biological processes, including cell differentiation, apoptosis, transcriptional regulation, signal transduction, and immunity.9–11 Here, we identified a novel function for TRIM3 as an E3 ubiquitin ligase for Beclin1. For the first time, we found that TRIM3 expression is increased in Ewing sarcoma tissues and up-regulated by EWS-FLI1. TRIM3 was also found to suppress autophagy in ES cells and it directly interacted with Beclin1, promoting proteasomal degradation of Beclin1, therefore suppressed autophagy in ES cells. In conclusion, we revealed the effect of TRIM3 on autophagy in ES cells in the current study.

Materials and Methods

Cell Culture and Tissues

NIH3T3, A673, and TC71 cells were obtained from American Type Culture Collection (Manassas, VA). All the cells were cultured in RPMI 1640 containing 10% FCS for normal condition. Cells were cultured in serum-free medium for starvation for indicated time to induce autophagy. Eight formalin-fixed paraffin-embedded (FFPE) specimens of Ewing’s sarcomas and eight normal soft tissues around bones were acquired from Department of Orthopedics, Qilu Hospital of Shandong University, China. Clinical characteristics of ES patients were provided (Table 1). The study protocol was approved by the Ethics Committee of Our Hospital and all patients gave written informed consent.

Table 1

Clinical Characteristics of ES Patients (n=8)

Patient	Age (years)	Sex	Primary Site	Metastasis	Translocation	Relapse/PD	Survival (Months)	Overall Outcome
1	12	F	Pelvis	BM	EWS-FLI1	No	48	Alive
2	15	F	Scapula	Bone, BM	EWS-FLI1	Yes	10	DOD
3	8	M	Rib	None	EWS-FLI1	No	72	Alive
4	11	M	Femur	Pulmonary	EWS-FLI1	No	48	Alive
5	13	M	Humerus	None	EWS-FLI1	Yes	26	DOD
6	6	F	Fibula	None	EWS-FLI1	No	72	Alive
7	16	M	Pelvis	Pulmonary	EWS-FLI1	No	36	Alive
8	15	F	Humerus	None	EWS-FLI1	Yes	54	DOD

Abbreviations: BM, bone marrow; DOD, died of disease.

Lentivirus and Plasmid

Lentivirus containing empty plasmid or EWS-FLI1 expression plasmid, TRIM3 expression plasmid, HA-tagged ub plasmids, shRNA-control plasmid and shRNA-TRIM3 plasmid were all constructed and bought from MDL biotechnology (MDL biotech, Beijing, China). Myc-tagged Beclin1 or Flag-tagged TRIM3 were obtained by PCR and cloned into the pCMV-Myc plasmid or pCMV6-Flag plasmid (Promega). The lentivirus particle was used to infect NIH3T3 for 3 days at 50 MOI with the presence of polybrene, puromycin selection was performed to establish the overexpression cell lines. Lipofectamine 2000 transfection reagent (Invitrogen) was used to transfect plasmids and siRNAs into ES cells.

RNA Analysis and ChIP Assays

The cells were collected in TRIzol reagent (Invitrogen, Carlsbad, CA). Total RNA was extracted using the TRIzol reagent according to the manufacturer’s instructions. A LightCycler (ABI PRISM 7000; Applied Biosciences) and a SYBR RT-PCR kit (Takara Biotechnology, Dalian, China) were used for real time PCR analysis. GAPDH was used as the internal control, thermocycling conditions were 1 cycle (95°C, 5 min) and 40 cycles (95°C, 15 sec; 57°C, 30 sec; 72°C, 30 sec) and the 2^-ΔΔCT method was used to evaluate the relative quantities of each amplified product in the samples.12 ChIP assay was performed as previously reported and the primer sequences for qPCR (as shown in Table 2) and ChIP-qPCR were used as described.13

Table 2

List of Primers Used in the Study

Number	Gene		Sequence (5ʹ–3ʹ)
1	TRIM3	F	GAG GGC AAG TTC AAG ACC AAG
		R	GGA AGG TAA AGA CGC AGC AAG
2	TRIM31	F	CCC ATC CCA CTC CCT GTT TC
		R	GCT GTC AGC CAC TCA CTC AG
3	TRIM32	F	TGT CCC TTT TGC AGC AAG ATT
		R	GAT CTT TAG CAC TGT CAG ATT
4	TRIM42	F	GCT CTG TGG ACA AAT TCG GG
		R	CCC CAC TTA GCT CGG TTC TT
5	GAPDH	F	CAC CCA CTC CTC CAC CTT TG
		R	CCA CCA CCC TGT TGC TGT AG

Western Blot Analysis and Immunoprecipitation

The cells were lysed using RIPA buffer (Thermo Scientific, Rockford, IL), and total protein in the supernatants was quantified using a BCA protein assay kit (Thermo Scientific, Waltham, MA). Immunoprecipitation (IP) and Western blot analysis were performed as described previously.14 Primary antibodies including anti-p62 (1:500, #sc-101542), anti-LC3 (1:500, #sc-398822), anti-FLI1 (1:500, #sc-22808) and anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (1: 1000, #sc-32233) were bought from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA), anti-TRIM3 (1:1000, #ab111840), anti-Beclin1 (1:1000, #ab207612), anti-Myc (1: 1000, #ab32), anti-Flag (1:1000, #ab49763) and anti-HA (1:1000, #ab9110) were obtained from Abcam (Abcam, Cambridge, USA).

Confocal Microscopic Analysis

The experiment was performed as described previously.15 All slides were observed under a confocal laser microscopy (LSM780, Carl Zeiss, Oberkochen, Germany).

Statistical Analysis

All data are presented as mean ± S.D. of three independent experiments. Statistical significance was determined using the two-tailed student’s t-test to compare two groups. One-way ANOVA was performed to compare three or more groups. If the ANOVA analysis was significant, the Newman-Keuls test was applied for comparison between each two groups. Data were considered significant at P < 0.05.

Results

Expression of TRIM3 Was Increased in ES Tissues

TRIM3 has been reported as an essential suppressor in glioblastomas, colorectal cancer and rheumatoid arthritis.16 In order to investigate the function of TRIM3 in ES, we examined the expression of TRIM3 in ES tissues at first. As shown in Figure 1A, the mRNA level of TRIM3 is significantly up-regulated in ES tissues compared with normal tissues. Consistently, the protein level of TRIM3 is also increased in ES tissues (Figure 1B). In addition, we also examined the expression of P62 which is well known as marker protein of autophagy, and we observed that P62 levels were also increased consistent with TRIM3 expression in ES tissues (Figure 1B). Taken together, these data suggested that expression of TRIM3 is increased in ES tissues.

Figure 1

Expression of TRIM3 was increased in ES tissues. (A) qPCR analysis of mRNA expression of TRIM3 in eight normal tissues or eight Ewing sarcoma tissues. (B) Western blot analysis of TRIM3 and P62 expression in three normal tissues or three Ewing sarcoma tissues. Data are representative of three independent experiments (mean ± SD). ***P < 0.001.

Expression of TRIM3 Was Regulated by EWS-FLI1

EWS-FLI1 induces the expression of many proteins, therefore we examined the relationship between TRIM3 and EWS-FLI1. As shown in Figure 2A, we detected the expression of various TRIM proteins including TRIM31, TRIM32, TRIM42, TRIM3, and only the expression of TRIM3 was markedly increased by EWS-FLI1 overexpression. EWS-FLI1 is known as a transcription factor to induce protein expression, we suspected if TRIM3 is a transcript target of EWS-FLI1. However, as shown in Figure 2B, ChIP-qPCR result demonstrated that EWS-FLI1 does not has the ability to interact with TRIM3 promoter, which meant that TRIM3 is not a transcript target of EWS-FLI1. Furthermore, we found the expression of TRIM3 was up-regulated in a dose dependent manner in EWS-FLI1 overexpressed cells (Figure 2C). Consistently, knockdown the expression of EWS-FLI1 also decreased TRIM3 expression. (Figure 2D). Taken together, these data suggested that TRIM3 expression is regulated by EWS-FLI1, however TRIM3 is not a transcript target of EWS-FLI1.

Figure 2

Expression of TRIM3 was regulated by EWS-FLI1. (A) qPCR analysis of mRNA expression of TRIM3, TRIM31, TRIM32, TRIM42 in NIH3T3 cells stable overexpressing control plasmid or EWS-FLI1 expression plasmid after starvation for 2 h. (B) ChIP assay and qPCR analysis were performed with fragmented chromatin from NIH3T3 cells stable overexpressing control plasmid or EWS-FLI1 expression plasmid after starvation for 2 h. (C) NIH3T3 cells were infected with increasing titer of EWS-FLI1-lentivirus, the protein levels of TRIM3 and EWS-FLI1 were examined by Western blot. (D) A673 cells were transfected with specific siRNAs for EWS-FLI1, the protein levels of TRIM3 and EWS-FLI1 were examined by Western blot. Data are representative of three independent experiments (mean ± SD). ***P < 0.001.

Overexpression of TRIM3 Inhibited Autophagy in ES Cells

In previous study, we found that EWS-FLI1 promotes autophagy in ES cells,13 therefore we supposed if TRIM3 could also regulate autophagy. Overexpression of TRIM3 in TC71 cells was confirmed as shown in Figure 3A. We observed that the expression of P62 was significantly increased and LC3-II level was decreased in TRIM3 overexpressed ES cells (Figure 3B and D). By using autophagy inhibitor Bafilomycin A1 (Baf A1), we observed that TRIM3 overexpression decreased autophagy flux (Figure 3C and E). Furthermore, we found that the formation of autophagosomes was suppressed by TRIM3 overexpression (Figure 3F and G). Taken together, these data suggested that overexpression of TRIM3 inhibits autophagy in ES cells.

Figure 3

Overexpression of TRIM3 inhibited autophagy in ES cells. (A) TC71 cells were transfected with TRIM3 expression plasmid or control plasmid, and overexpression of TRIM3 was examined by Western blot. (B) Western blot analysis of P62, LC3-I, LC3-II and GAPDH in TRIM3 overexpressed TC71 cells after starvation for 2 h. (C) For autophagy flux assay, TRIM3 overexpressed TC71 cells were treated with or without an autophagy inhibitor baflomycine A1 (Baf A1, 0.1 μM) for 3 h, LC3-II levels were examined by Western blot. (D) Band intensity of P62 and LC3-II were quantified and normalized to the GAPDH in (B). (E) LC3-II accumulation was quantified and normalized to the GAPDH in (C). (F) TC71 cells transfected with TRIM3 expression plasmid or control plasmid were inspected under confocal laser microscopy to detect LC3 puncta by immunofluorescence after starvation for 2 h. (G) LC3 puncta number per cell in (F) was quantified using the Image J program, and 30 to 60 cells chosen in random were counted. Data are representative of three independent experiments (mean ± SD). *p<0.05; ***P < 0.001.

Silencing of TRIM3 Promoted Autophagy in ES Cells

ShRNA plasmid of TRIM3 was used to knockdown the expression of TRIM3, and the effect of shRNA was examined (Figure 4A). After transfection with shRNA-TRIM3, P62 level was greatly decreased and LC3-II expression was increased (Figure 4B and D), autophagy flux was enhanced (Figure 4C and E) as well as the increased formation of autophagosomes in TRIM3-silenced ES cells (Figure 4F and G). Taken together, these data suggested that silencing of TRIM3 promotes autophagy in ES cells.

Figure 4

Silencing of TRIM3 promoted autophagy in ES cells. (A) A673 cells were transfected with shRNA-TRIM3 plasmid or shRNA-control plasmid, and the expression of TRIM3 was examined by Western blot. (B) Western blot analysis of P62, LC3-I, LC3-II and GAPDH in TRIM3 silenced A673 cells after starvation for 4 h. (C) For autophagy flux assay, TRIM3 silenced A673 cells were treated with or without an autophagy inhibitor baflomycine A1 (Baf A1, 0.1 μM) for 3 h, LC3-II levels were examined by Western blot. (D) Band intensity of P62 and LC3-II were quantified and normalized to the GAPDH in (B). (E) LC3-II accumulation was quantified and normalized to the GAPDH in (C). (F) A673 cells transfected with shRNA-TRIM3 plasmid or shRNA-control plasmid were inspected under confocal laser microscopy to detect LC3 puncta by immunofluorescence after starvation for 4 h. (G) LC3 puncta number per cell in (F) was quantified using the Image J program, and 30 to 60 cells chosen in random were counted. Data are representative of three independent experiments (mean ± SD). *p<0.05; ***P < 0.001.

TRIM3 Interacted with Beclin1 and Promoted K48-Linked Polyubiquitination of Beclin1

Beclin1 is a well-known key regulator of autophagy, we supposed if TRIM3 regulate autophagy through Beclin1. At first, we detected the expression of Beclin1 in TRIM3 overexpressed ES cells, and we found that TRIM3 significantly suppressed Beclin1 expression in a dose dependent manner and the decreased expression induced by TRIM3 was restored by Mg132 treatment (Figure 5A and B). We also examined the interaction between TRIM3 and Beclin1, and we observed that TRIM3 directly interacted with Beclin1 (Figure 5C). Endogenous interaction was also examined, and we found that TRIM3 expression is increased first and then decreased at 120mins after starvation treatment, the interaction between TRIM3 and Beclin1 is strongest at 120mins of starvation (Figure 5D). At last, we detected the level of polyubiquitination of Beclin1 in TRIM3 overexpressed ES cells, we found that overexpression TRIM3 markedly improved K48-linked polyubiquitination of Beclin1 but has no effect on level of K63-linked polyubiquitination (Figure 5E), therefore TRIM3 promoted the proteasomal degradation of Beclin1, leading to the suppression of autophagy in ES cells.

Figure 5

TRIM3 interacted with Beclin1 and promoted K48-linked polyubiquitination of Beclin1. (A) TC71 cells were transfected with increased dose of TRIM3, and the protein level of Beclin1 was detected by Western blot. (B) TC71 cells were transfected with TRIM3 and Beclin1 then treated with proteasome inhibitor Mg132 for 4 h. (C) TC71 cells were transfected with TRIM3 and Beclin1nd the interaction was detected by co-IP assay and Western blot. (D) Endogenous interaction between TRIM3 and Beclin1 was detected in TC71 cells at indicated treatment time. (E) TC71 cells were transfected with TRIM3, Beclin1 together with WT, K48 or K63-linked ubiquitin plasmid. The polyubiquitination level of Beclin1 was examined by Western blot. Data are representative of three independent experiments (mean ± SD).

Discussion

ES is an aggressive bone and soft tissue malignant tumor that primarily affects children, and young adults.2 The survival rates for patients with metastatic disease have not improved in over 20 years.17 Thus, novel therapeutic targets and increased understanding of the metastatic mechanism of ES are required. Tripartite motif (TRIM) family proteins are composed of over 70 members in humans.18 TRIM proteins have been implicated in many biological processes including cell differentiation, apoptosis, transcriptional regulation, and signaling transduction.7,8 The characteristic structure of TRIM proteins is the presence of a RING (R) domain, one or two B-boxes (B), and a coiled coil (CC) domain.9 In the current study, we investigated the role of TRIM3 in ES. We found that the expression of TRIM3 is specific increased in ES tissues compared with the normal tissues. We also observed that the expression of TRIM3 is associated with EWS-FLI1 expression, however, TRIM3 was found not being a transcript target of EWS-FLI1, and the precise mechanism about EWS-FLI1 induced TRIM3 expression still need further study.

Autophagy plays great roles in the clearance of long-lived proteins, aggregates and damaged organelles, and dysregulation of autophagy is highly associated with cancer, particularly in tumorigenesis and chemotherapy resistance.13 In the current study, we found that TRIM3 could regulate autophagy in ES cells. Overexpression of TRIM3 significantly inhibits autophagy, as evidenced by the increases in the amount of P62 (SQSTM1) and decreases in the amount of LC3B-II, two important markers of autophagy, as well as the increased LC3 puncta in cells. Consistently, the level of P62 was up-regulated and LC3B-II was down-regulated in TRIM3-silenced ES cells. These findings indicated that TRIM3 plays great roles in the process of autophagy in ES.

To further explore the potential mechanisms that how could TRIM3 regulate autophagy in ES cells, we examined the relationship between TRIM3 and Beclin1, which has been demonstrated to initiate autophagosome formation.19 Beclin-1 dysfunction has been identified in a number of disorders, including cancer, aging and degenerative diseases; for example, overexpression of Beclin-1 markedly promotes autophagic cell death in leukemia cells.20 In the study, we found that the expression of Beclin1 is down-regulated by TRIM3 overexpression in a dose-dependent manner. The interaction between TRIM3 and Beclin1 was also proved by IP assay, indicated that TRIM3 directly interact with Beclin1. Most importantly, we found that the K48-linked polyubiquitination level of Beclin1 was increased in TRIM3 overexpressed ES cells, which meant that TRIM3 increased K48-linked polyubiquitination of Beclin1 and promoted Beclin1 degradation, and finally down-regulated the autophagy in ES cells.

In conclusion, in the present research, for the first time we revealed the function of TRIM3 in ES and we showed the effect of TRIM3 on autophagy in ES cells, and these findings may provide ideals for ES researches.