Genomic Medicine Institute, Lerner Research Institute of Cleveland Clinic, Cleveland, OH, U.SA.
Department of Pathology, Karamay Central Hospital, Karamay, China.
Biochem J. 2022 Apr 14;479(7):839-855. doi: 10.1042/BCJ20220055.
α1-antitrypsin (AAT) is a serine protease inhibitor synthesized in hepatocytes and protects the lung from damage by neutrophil elastase. AAT gene mutations result in AAT deficiency (AATD), which leads to lung and liver diseases. The AAT Z variant forms polymer within the endoplasmic reticulum (ER) of hepatocytes and results in reduction in AAT secretion and severe disease. Previous studies demonstrated a secretion defect of AAT in LMAN1 deficient cells, and mild decreases in AAT levels in male LMAN1 and MCFD2 deficient mice. LMAN1 is a transmembrane lectin that forms a complex with a small soluble protein MCFD2. The LMAN1-MCFD2 protein complex cycles between the ER and the Golgi. Here, we report that LMAN1 and MCFD2 knockout (KO) HepG2 and HEK293T cells display reduced AAT secretion and elevated intracellular AAT levels due to a delayed ER-to-Golgi transport of AAT. Secretion defects in KO cells were rescued by wild-type LMAN1 or MCFD2, but not by mutant proteins. Elimination of the second glycosylation site of AAT abolished LMAN1 dependent secretion. Co-immunoprecipitation experiment in MCFD2 KO cells suggested that AAT interaction with LMAN1 is independent of MCFD2. Furthermore, our results suggest that secretion of the Z variant, both monomers and polymers, is also LMAN1-dependent. Results provide direct evidence supporting that the LMAN1-MCFD2 complex is a cargo receptor for the ER-to-Golgi transport of AAT and that interactions of LMAN1 with an N-glycan of AAT is critical for this process. These results have implications in production of recombinant AAT and in developing treatments for AATD patients.
α1-抗胰蛋白酶(AAT)是一种在肝细胞中合成的丝氨酸蛋白酶抑制剂,可保护肺部免受中性粒细胞弹性蛋白酶的损伤。AAT 基因突变导致 AAT 缺乏症(AATD),从而导致肺部和肝脏疾病。AAT Z 变体在肝细胞的内质网(ER)内形成聚合物,导致 AAT 分泌减少和严重疾病。以前的研究表明,LMAN1 缺乏的细胞中 AAT 分泌存在缺陷,并且 LMAN1 和 MCFD2 缺乏的雄性小鼠中 AAT 水平轻度降低。LMAN1 是一种跨膜凝集素,它与一种小的可溶性蛋白 MCFD2 形成复合物。LMAN1-MCFD2 蛋白复合物在 ER 和高尔基体之间循环。在这里,我们报告 LMAN1 和 MCFD2 敲除(KO)HepG2 和 HEK293T 细胞显示 AAT 分泌减少和细胞内 AAT 水平升高,这是由于 AAT 的 ER 到高尔基体运输延迟所致。KO 细胞中的分泌缺陷可通过野生型 LMAN1 或 MCFD2 挽救,但不能通过突变蛋白挽救。AAT 的第二个糖基化位点的消除消除了依赖于 LMAN1 的分泌。在 MCFD2 KO 细胞中的共免疫沉淀实验表明,AAT 与 LMAN1 的相互作用独立于 MCFD2。此外,我们的结果表明,Z 变体的单体和聚合物的分泌也依赖于 LMAN1。结果提供了直接证据,支持 LMAN1-MCFD2 复合物是 AAT 的 ER 到高尔基体运输的货物受体,并且 LMAN1 与 AAT 的 N-聚糖的相互作用对于该过程至关重要。这些结果对重组 AAT 的生产和开发 AATD 患者的治疗具有重要意义。