Mice deficient in UXT exhibit retinitis pigmentosa-like features via aberrant autophagy activation

Autophagy. 2021 Aug;17(8):1873-1888. doi: 10.1080/15548627.2020.1796015. Epub 2020 Aug 2.

Abstract

UXT (ubiquitously expressed prefoldin like chaperone), a small chaperone-like protein, is widely expressed in diverse human and mouse tissues and is more abundant in retina and kidney. However, the functional characterization of UXT at tissue level was largely unknown. Here, we reported that mice deficient in UXT exhibited salient features of retinal degenerative disease, similar to retinitis pigmentosa. Conditional knockout (CKO) of Uxt led to retinal degeneration and pigmentation in mice retina along with significant alterations of retinitis pigmentosa-related genes, which indicated UXT might be associated with retinal degenerative disease sharing key features to retinitis pigmentosa. Consistently, the electroretinogram (ERG) responses were dramatically impaired in uxt CKO retinas. Strong degenerative features were observed in uxt CKO retinas, including specific and progressive reduction of photoreceptor cells and increased numbers of apoptotic cells. Intriguingly, macroautophagic/autophagic flux was enhanced in uxt CKO retina. Mechanistically, we found UXT was indispensable to suppress photoreceptor apoptotic cell death by inhibiting autophagy through regulating the activity of MTOR (mechanistic target of rapamycin kinase), a key negative regulator of autophagy. Conversely, knockdown of UXT induced the robust expression of the canonical autophagy-related genes and boosted autophagic flux and apoptosis, finally resulting in severe retina degeneration in uxt CKO mice. Taken together, our study reveals a vital role of UXT in preventing retina from degeneration. The loss of UXT results in a hyper-autophagic state leading to massive retinal degeneration. Therefore, UXT may be a crucial target for retinal degenerative disease.Abbreviations: 3-ma: 3-methyladenine; casp3: caspase 3; cko: conditional knockout; erg: electroretinogram; gapdh: glyceraldehyde-3-phosphate dehydrogenase; map1lc3b/lc3b: microtubule-associated protein 1 light chain 3; mtor: mechanistic target of rapamycin kinase; parp: poly (adp-ribose) polymerase family; rna-seq: rna sequencing; rp: retinitis pigmentosa; rps6kb1/s6k: ribosomal protein s6 kinase b1; sqstm1: sequestosome 1; tunel: terminal deoxynucleotidyl transferase mediated dutp nick-end labeling; uxt: ubiquitously expressed prefoldin like chaperone.

Keywords: Apoptosis; MTOR; UXT; autophagy; degeneration; photoreceptor; retinitis pigmentosa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Autophagy / genetics*
  • Autophagy / physiology*
  • Cell Cycle Proteins / deficiency*
  • Cell Cycle Proteins / metabolism
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Molecular Chaperones / metabolism
  • Retina / metabolism
  • Retinal Degeneration / metabolism
  • Retinitis Pigmentosa / genetics
  • Retinitis Pigmentosa / metabolism*

Substances

  • Cell Cycle Proteins
  • Molecular Chaperones
  • UXT protein, human
  • UXT protein, mouse

Grants and funding

This work was supported by the National Natural Science Foundation of China [31601068]; National Natural Science Foundation of China [81672029]; National Natural Science Foundation of China [31730018]; “Double First-Class” Project of China Pharmaceutical University [CPU2018GF10]; Postgraduate Research & Practice Innovation Program of Jiangsu Province [3322000026]; Jiangsu Innovative and Entrepreneurial Talents Program, the National New Drug Innovation Major Project of China [2017ZX09309027]; National Key R&D Program of China [2016YFA0501800]; Open Project of State Key Laboratory of Natural Medicines [SKLNMZZCX201802]; “Double First-Class” Project of China Pharmaceutical University [CPU2018GF10]; Priority Academic Program Development of Jiangsu Higher Education Institutions [PAPD].