Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Instituto de Biologia Molecular e Celular, Porto, Portugal.
Autophagy. 2023 Feb;19(2):426-439. doi: 10.1080/15548627.2022.2074105. Epub 2022 May 19.
Within the thymus, thymic epithelial cells (TECs) provide dedicated thymic stroma microenvironments for T cell development. Because TEC functionality is sensitive to aging and cytoablative therapies, unraveling the molecular elements that coordinate their thymopoietic role has fundamental and clinical implications. Particularly, the selection of CD4 T cells depends on interactions between TCRs expressed on T cell precursors and self-peptides:MHC II complexes presented by cortical TECs (cTECs). Although the macroautophagy/autophagy-lysosomal protein degradation pathway is implicated in CD4 T cell selection, the molecular mechanism that controls the generation of selecting MHC II ligands remains elusive. LAMP2 (lysosomal-associated membrane protein 2) is a well-recognized mediator of autolysosome (AL) maturation. We showed that LAMP2 is highly expressed in cTECs. Notably, genetic inactivation of in thymic stromal cells specifically impaired the development of CD4 T cells that completed positive selection, without misdirecting MHC II-restricted cells into the CD8 lineage. Mechanistically, defects in autophagy in -deficient cTECs were linked to alterations in MHC II processing, which was associated with a marked reduction in CD4 TCR repertoire diversity selected within the -deficient thymic stroma. Together, our findings suggest that LAMP2 interconnects the autophagy-lysosomal axis and the processing of selecting self-peptides:MHC II complexes in cTECs, underling its implications for the generation of a broad CD4 TCR repertoire.: AIRE: autoimmune regulator (autoimmune polyendocrinopathy candidiasis ectodermal dystrophy); AL: autolysosome; AP: autophagosome; Baf-A1: bafilomycin A; B2M: beta-2 microglobulin; CTSL: cathepsin L; CD74/Ii: CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated); CFSE: carboxyfluorescein succinimidyl ester; CFU: colony-forming unit; CLIP: class II-associated invariant chain peptides; cTECs: cortical TECs dKO: double knockout; DN: double negative; DP: double positive; ENPEP/LY51: glutamyl aminopeptidase; FOXP3: forkhead box; P3 IFNG/IFNγ: interferon gamma; IKZF2/HELIOS: IKAROS family zinc finger 2; IL2RA/CD25: interleukin 2 receptor, alpha chain; KO: knockout; LAMP2: lysosomal-associated membrane protein 2; LIP: lymphopenia-induced proliferation; Lm: MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; MHC: major histocompatibility complex; mTECs: medullary TECs; PRSS16/TSSP: protease, serine 16 (thymus); SELL/CD62L: selectin, lymphocyte; SP: single positive; TCR: T cell receptor; TCRB: T cell receptor beta chain; TECs: thymic epithelial cells; UEA-1: agglutinin-1; WT: wild-type.
在胸腺中,胸腺上皮细胞 (TEC) 为 T 细胞发育提供专用的胸腺基质微环境。由于 TEC 的功能对衰老和细胞毒性疗法敏感,因此阐明协调其胸腺生成作用的分子要素具有基础和临床意义。特别是,CD4 T 细胞的选择取决于 T 细胞前体上表达的 TCR 与皮质 TEC(cTEC)上呈现的自身肽:MHC II 复合物之间的相互作用。尽管宏自噬/自噬溶酶体蛋白降解途径与 CD4 T 细胞选择有关,但控制选择 MHC II 配体的分子机制仍不清楚。LAMP2(溶酶体相关膜蛋白 2)是公认的自噬体(AL)成熟的介质。我们发现 LAMP2 在 cTEC 中高度表达。值得注意的是,特异性敲除 基因会损害完成阳性选择的 CD4 T 细胞的发育,而不会将 MHC II 限制性细胞错误引导到 CD8 谱系。从机制上讲,-缺陷的 cTEC 中的自噬缺陷与 MHC II 加工的改变有关,这与在 -缺陷的胸腺基质中选择的 CD4 TCR 库多样性明显减少有关。总之,我们的发现表明 LAMP2 连接自噬溶酶体轴和 cTEC 中选择自身肽:MHC II 复合物的加工,这表明它对生成广泛的 CD4 TCR 库具有重要意义。:AIRE:自身免疫调节因子(自身免疫性多内分泌腺病念珠菌病外胚层营养不良);AL:自噬体;AP:自噬体;Baf-A1:巴弗霉素 A;B2M:β-2 微球蛋白;CTSL:组织蛋白酶 L;CD74/Ii:CD74 抗原(主要组织相容性复合体 II 抗原相关的不变多肽);CFSE:羧基荧光素琥珀酰亚胺酯;CFU:集落形成单位;CLIP:II 类相关不变链肽;cTECs:皮质 TECs dKO:双敲除;DN:双阴性;DP:双阳性;ENPEP/LY51:谷氨酰氨肽酶;FOXP3:叉头框;P3 IFNG/IFNγ:干扰素γ;IKZF2/HELIOS:Ikaros 家族锌指 2;IL2RA/CD25:白细胞介素 2 受体,α 链;KO:敲除;LAMP2:溶酶体相关膜蛋白 2;LIP:淋巴细胞减少诱导的增殖;LM:MAP1LC3/LC3:微管相关蛋白 1 轻链 3;MHC:主要组织相容性复合体;mTECs:髓质 TECs;PRSS16/TSSP:蛋白酶,丝氨酸 16(胸腺);SELL/CD62L:选择素,淋巴细胞;SP:单阳性;TCR:T 细胞受体;TCRB:T 细胞受体 β 链;TECs:胸腺上皮细胞;UEA-1:凝集素-1;WT:野生型。