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该新型分子通过阻止 BBC3 与 HSPA8 的相互作用抑制自噬降解,从而诱导滋养细胞凋亡。

The novel suppresses autophagy degradation of BBC3 by preventing its interactions with HSPA8 to induce trophoblast cell apoptosis.

机构信息

Research Center for Environment and Female Reproductive Health, the Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, China.

Key Laboratory of Environment and Female Reproductive Health, West China School of Public Health, Sichuan University, Chengdu, Sichuan, China.

出版信息

Autophagy. 2024 Oct;20(10):2255-2274. doi: 10.1080/15548627.2024.2362122. Epub 2024 Jun 6.

Abstract

Abnormal expression of long non-coding RNAs (lncRNAs) is associated with the dysfunctions of human trophoblast cells and the occurrence of miscarriage (abnormal early embryo loss). BBC3/PUMA (BCL2 binding component 3) plays significant roles in regulation of cell apoptosis. However, whether specific lncRNAs might regulate BBC3 in trophoblast cells and further induce apoptosis and miscarriage remains completely unclear. Through screening, we identified a novel , which was significantly highly expressed in villous tissues of recurrent miscarriage (RM) patients relative to their healthy control (HC) group. suppressed chaperone-mediated autophagy (CMA) degradation of BBC3, promoted trophoblast cell apoptosis, and was associated with miscarriage. In mechanism, downregulated the expression levels of chaperone molecules HSPA8 and LAMP2A in trophoblast cells. Meanwhile, (mainly SO2 region in F2 fragment) and HSPA8 competitively bound with the RVLYNL patch on BBC3, which prevented BBC3 from interactions with HSPA8 and impaired the formation of BBC3-HSPA8-LAMP2A complex for CMA degradation of BBC3. Thus, upregulated the BBC3-CASP9-CASP3 pathway and induced trophoblast cell apoptosis. In villous tissues, was highly expressed, CMA degradation of BBC3 was suppressed, and the apoptosis levels were higher in RM vs HC villous tissues, all of which were associated with miscarriage. Interestingly, knockdown of murine could efficiently suppress placental apoptosis and alleviate miscarriage in a mouse miscarriage model. Taken together, our results indicated that and BBC3 played important roles in trophoblast cell apoptosis and miscarriage and might act as attractive targets for miscarriage treatment.: 7-AAD: 7-aminoactinomycin D; BaP: benzopyrene; BBC3/PUMA: BCL2 binding component 3; ChIP: chromatin immunoprecipitation; CHX: cycloheximide; CMA: chaperone-mediated autophagy; CQ: chloroquine; DMSO: dimethyl sulfoxide; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; HC: healthy control; HSPA8: heat shock protein family A (Hsp70) member 8; IP: immunoprecipitation; LAMP2A: lysosomal associated membrane protein 2; LncRNA: long non-coding RNA; mRNA: messenger RNA; MT: mutant-type; NC: negative control; NSO: nonspecific oligonucleotide; PARP1: poly(ADP-ribose) polymerase 1; RIP: RNA immunoprecipitation; RM: recurrent miscarriage; TBP: TATA-box binding protein; WT: wild-type.

摘要

长非编码 RNA(lncRNA)的异常表达与人类滋养层细胞功能障碍和流产(早期胚胎异常丢失)的发生有关。BCL2 结合成分 3(BBC3/PUMA)在细胞凋亡调控中发挥重要作用。然而,特定的 lncRNA 是否可能调节滋养层细胞中的 BBC3,并进一步诱导细胞凋亡和流产,目前仍完全不清楚。通过筛选,我们鉴定了一个新的 lncRNA,它在复发性流产(RM)患者的绒毛组织中显著高表达,而在其健康对照组(HC)中低表达。lncRNA 通过抑制 BBC3 的伴侣介导的自噬(CMA)降解,促进滋养层细胞凋亡,并与流产有关。在机制上,lncRNA 下调了滋养层细胞中伴侣分子 HSPA8 和 LAMP2A 的表达水平。同时,lncRNA (主要是 F2 片段中的 SO2 区域)与 BBC3 上的 RVLYNL 补丁竞争结合,阻止 BBC3 与 HSPA8 相互作用,并损害 BBC3-HSPA8-LAMP2A 复合物的形成,从而抑制 BBC3 的 CMA 降解。因此,lncRNA 上调了 BBC3-CASP9-CASP3 通路,并诱导滋养层细胞凋亡。在绒毛组织中,lncRNA 高表达,BBC3 的 CMA 降解受到抑制,RM 与 HC 绒毛组织中的细胞凋亡水平升高,均与流产有关。有趣的是,小鼠 lncRNA 的敲低可有效抑制胎盘细胞凋亡并减轻小鼠流产模型中的流产。总之,我们的研究结果表明,lncRNA 和 BBC3 在滋养层细胞凋亡和流产中发挥重要作用,可能成为流产治疗的有吸引力的靶点。7-AAD:7-氨基放线菌素 D;BaP:苯并芘;BBC3/PUMA:BCL2 结合成分 3;ChIP:染色质免疫沉淀;CHX:环己酰亚胺;CMA:伴侣介导的自噬;CQ:氯喹;DMSO:二甲基亚砜;GAPDH:甘油醛-3-磷酸脱氢酶;HC:健康对照组;HSPA8:热休克蛋白家族 A(Hsp70)成员 8;IP:免疫沉淀;LAMP2A:溶酶体相关膜蛋白 2;LncRNA:长非编码 RNA;mRNA:信使 RNA;MT:突变型;NC:阴性对照;NSO:非特异性寡核苷酸;PARP1:多聚(ADP-核糖)聚合酶 1;RIP:RNA 免疫沉淀;RM:复发性流产;TBP:TATA 框结合蛋白;WT:野生型。

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本文引用的文献

1
BPDE, the Migration and Invasion of Human Trophoblast Cells, and Occurrence of Miscarriage in Humans: Roles of a Novel .
Environ Health Perspect. 2023 Jan;131(1):17009. doi: 10.1289/EHP10477. Epub 2023 Jan 31.
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Lnc-HZ08 regulates BPDE-induced trophoblast cell dysfunctions by promoting PI3K ubiquitin degradation and is associated with miscarriage.
Cell Biol Toxicol. 2022 Apr;38(2):291-310. doi: 10.1007/s10565-021-09606-z. Epub 2021 Apr 16.
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