Chaperone-mediated autophagy degrades SERPINA1<sup>E342K</sup>/α1-antitrypsin Z variant and alleviates cell stress

Chaperone-mediated autophagy (CMA) is a specific form of autophagy that selectively targets proteins containing a KFERQ-like motif and relies on the chaperone protein HSPA8/HSC70 for substrate recognition. In SERPINA1/a1-antitrypsin deficiency (AATD), a disease characterized by the hepatic buildup of the SERPINA1<sup>E342K</sup>/ATZ, CMA’s role had been unclear. This work demonstrates the critical role that CMA plays in preventing SERPINA1<sup>E342K</sup>/ATZ accumulation; suppressing CMA worsens SERPINA1<sup>E342K</sup>/ATZ accumulation while activating it through chemical stimulation or LAMP2A overexpression promotes SERPINA1<sup>E342K</sup>/ATZ breakdown. Specifically, SERPINA1<sup>E342K</sup>/ATZ’s <sub>121</sub>QELLR<sub>125</sub> motif is critical for HSPA8/HSC70 recognition and LAMP2A’s charged C-terminal cytoplasmic tail is vital for substrate binding, facilitating CMA-mediated degradation of SERPINA1<sup>E342K</sup>/ATZ. This selective activation of CMA operates independently of other autophagy pathways and alleviates SERPINA1<sup>E342K</sup>/ATZ aggregate-induced cellular stress. In vivo administration of AR7 promotes hepatic SERPINA1<sup>E342K</sup>/ATZ elimination and mitigates hepatic SERPINA1<sup>E342K</sup>/ATZ aggregation pathology. These findings highlight CMA’s critical function in cellular protein quality control of SERPINA1<sup>E342K</sup>/ATZ and place it as a novel target for AATD treatment. <b>Abbreviation:</b> AR7: atypical retinoid 7; ATG16L1: autophagy related 16 like 1; AATD: SERPINA1/alpha-1 antitrypsin deficiency; CHX: cycloheximide; CMA: chaperone-mediated autophagy; CQ: chloroquine; ER: endoplasmic reticulum; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; HSPA8/HSC70: heat shock protein family A (Hsp70) member 8; LAMP2A: lysosomal associated membrane protein 2A; LAMP2B: lysosomal associated membrane protein 2B; LAMP2C: lysosomal associated membrane protein 2C; MG132: carbobenzoxy-L-leucyl-L-leucyl-L-leucinal; PAS-D: periodic acid-Schiff plus diastase; SERPINA1/A1AT: serpin family A member 1; SERPINA1<sup>E342K</sup>/ATZ: Z variant of SERPINA1; TMRE: tetramethyl rhodamine ethyl ester perchlorate.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28637320
Primary Topic
Autophagy in Disease and Therapy
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article
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article

Chaperone-mediated autophagy degrades SERPINA1E342K/α1-antitrypsin Z variant and alleviates cell stress

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Autophagy in Disease and Therapy
article

Chaperone-mediated autophagy degrades SERPINA1E342K/α1-antitrypsin Z variant and alleviates cell stress

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Abstract

Chaperone-mediated autophagy (CMA) is a specific form of autophagy that selectively targets proteins containing a KFERQ-like motif and relies on the chaperone protein HSPA8/HSC70 for substrate recognition. In SERPINA1/a1-antitrypsin deficiency (AATD), a disease characterized by the hepatic buildup of the SERPINA1<sup>E342K</sup>/ATZ, CMA’s role had been unclear. This work demonstrates the critical role that CMA plays in preventing SERPINA1<sup>E342K</sup>/ATZ accumulation; suppressing CMA worsens SERPINA1<sup>E342K</sup>/ATZ accumulation while activating it through chemical stimulation or LAMP2A overexpression promotes SERPINA1<sup>E342K</sup>/ATZ breakdown. Specifically, SERPINA1<sup>E342K</sup>/ATZ’s <sub>121</sub>QELLR<sub>125</sub> motif is critical for HSPA8/HSC70 recognition and LAMP2A’s charged C-terminal cytoplasmic tail is vital for substrate binding, facilitating CMA-mediated degradation of SERPINA1<sup>E342K</sup>/ATZ. This selective activation of CMA operates independently of other autophagy pathways and alleviates SERPINA1<sup>E342K</sup>/ATZ aggregate-induced cellular stress. In vivo administration of AR7 promotes hepatic SERPINA1<sup>E342K</sup>/ATZ elimination and mitigates hepatic SERPINA1<sup>E342K</sup>/ATZ aggregation pathology. These findings highlight CMA’s critical function in cellular protein quality control of SERPINA1<sup>E342K</sup>/ATZ and place it as a novel target for AATD treatment. <b>Abbreviation:</b> AR7: atypical retinoid 7; ATG16L1: autophagy related 16 like 1; AATD: SERPINA1/alpha-1 antitrypsin deficiency; CHX: cycloheximide; CMA: chaperone-mediated autophagy; CQ: chloroquine; ER: endoplasmic reticulum; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; HSPA8/HSC70: heat shock protein family A (Hsp70) member 8; LAMP2A: lysosomal associated membrane protein 2A; LAMP2B: lysosomal associated membrane protein 2B; LAMP2C: lysosomal associated membrane protein 2C; MG132: carbobenzoxy-L-leucyl-L-leucyl-L-leucinal; PAS-D: periodic acid-Schiff plus diastase; SERPINA1/A1AT: serpin family A member 1; SERPINA1<sup>E342K</sup>/ATZ: Z variant of SERPINA1; TMRE: tetramethyl rhodamine ethyl ester perchlorate.

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Chaperone-mediated autophagy degrades SERPINA1<sup>E342K</sup>/α1-antitrypsin Z variant and alleviates cell stress · Figshare (2025) | TGRS Research Map | TGRS