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Updated: Mar 22, 2026

Assessing Autophagic Flux by Measuring LC3, p62, and LAMP1 Co-localization Using Multispectral Imaging Flow Cytometry
Published on: July 21, 2017
The germline-enriched Ppp1r36 promotes autophagy
Qinghua Zhang1, Maomao Gao2, Ying Zhang2
1Department of Cell Biology, Wuhan 430072, P. R. China.
Protein Phosphatase 1 regulatory subunit 36 (Ppp1r36) enhances autophagy during spermatogenesis. This study reveals Ppp1r36
Area of Science:
- Reproductive Biology
- Cellular Biology
- Molecular Biology
Background:
- Spermatogenesis, the generation of haploid sperm, involves complex regulation.
- The precise role and regulation of autophagy in germ cell development are not fully understood.
Purpose of the Study:
- To investigate the role of Ppp1r36 in spermatogenesis and its connection to autophagy.
- To elucidate the molecular mechanisms by which Ppp1r36 influences autophagy during male germ cell development.
Main Methods:
- Expression analysis of Ppp1r36 and autophagy marker LC3 in testes.
- Autophagy flux assays using tandem fluorescent reporters (mCherry-GFP-LC3).
- Co-immunoprecipitation to assess protein interactions (Ppp1r36 and Atg16L1).
Main Results:
- Ppp1r36 is expressed in testes during spermatogenesis, mirroring the pattern of active autophagy marker LC3-II.
- Autophagy is upregulated around 21 days postpartum, coinciding with the first wave of spermatogenesis.
- Ppp1r36 promotes autophagosome formation and is associated with Atg16L1, confirming its role in starvation-induced autophagy.
Conclusions:
- Ppp1r36, a regulatory subunit of protein phosphatase 1, plays a significant role in enhancing autophagy during spermatogenesis.
- The findings suggest Ppp1r36 is a key regulator of autophagy in male germ cells, impacting their development.
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