4.6 Article

iTRAQ-based proteomics of testicular interstitial fluid during aging in mice

Journal

THERIOGENOLOGY
Volume 175, Issue -, Pages 44-53

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.theriogenology.2021.08.034

Keywords

Aging; iTRAQ; Proteomics; Testicular interstitial fluid

Funding

  1. Guangdong Natural Science Foundation [2020A151501523]
  2. 5010 Project of Clinical Research in Sun Yat-Sen University [2019016]
  3. National Natural Science Foundation of China [81971314]

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This study identified 1477 proteins in murine TIF, with 706 proteins showing a linear change trend with age and 45 age-related DEPs identified. Bioinformatic analyses revealed that these proteins were involved in actin cytoskeleton organization, intrinsic apoptotic signaling pathway, and regulation of protein transport. Comparative analysis with relevant proteomes further revealed the characteristics of mouse TIF proteome.
Advancing age is associated with a decline in fertility and testicular function in males. The testicular interstitial fluid (TIF) bathing the seminiferous tubules and testicular interstitium is considered an important part of the testicular microenvironment. However, the TIF proteome in mice and whether it changes with age remain unclear. This study aimed to map the TIF proteome and identify differentially abundant proteins (DEPs) among young, middle-aged, and old mice using isobaric tags for relative and absolute quantification (iTRAQ) coupled with liquid chromatography-tandem mass spectrometry. A total of 1477 proteins were identified in murine TIF. The abundance of 706 proteins showed a linear change trend with age, of which 360 and 346 proteins increased and decreased, respectively. In addition, 45 age-related DEPs were identified (P < 0.05, with at least 1.2-fold up-or downregulation). Bioinformatic analyses revealed that these proteins were involved in actin cytoskeleton organization, intrinsic apoptotic signaling pathway, and regulation of protein transport. Comparative analysis with relevant proteomes previously reported further revealed the characteristics of mouse TIF proteome. Moreover, two of the age-related DEPs (Fga and Qsox1) were also found to be age-related differentially expressed proteins in human blood plasma and senescence-related secretome of human peritubular myoid cells. Taken together, these findings may represent the foundation for a better understanding of the molecular function of TIF and testicular aging. (c) 2021 Published by Elsevier Inc.

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