Abstract

Gravity change affects many immunological systems. We investigated the effects of hypergravity (2G) on murine thymic cells. Exposure of mice to 2G for three days reduced the frequency of CD4+CD8+ thymocytes (DP) and mature medullary thymic epithelial cells (mTECs), accompanied by an increment of keratin-5 and keratin-8 double-positive (K5+K8+) TECs that reportedly contain TEC progenitors. Whereas the reduction of DP was recovered by a 14-day exposure to 2G, the reduction of mature mTECs and the increment of K5+K8+ TEC persisted. Interestingly, a surgical lesion of the inner ear’s vestibular apparatus inhibited these hypergravity effects. Quantitative PCR analysis revealed that the gene expression of Aire and RANK that are critical for mTEC function and development were up-regulated by the 3-day exposure and subsequently down-regulated by the 14-day exposure to 2G. Unexpectedly, this dynamic change in mTEC gene expression was independent of the vestibular apparatus. Overall, data suggest that 2G causes a temporary reduction of DP and a persistent reduction of mature mTECs in a vestibular system-dependent manner, and also dysregulates mTEC gene expression without involving the vestibular system. These data might provide insight on the impact of gravity change on thymic functions during spaceflight and living.

Highlights

  • Spaceflight affects various immune systems [1,2,3]

  • We describe that hypergravity causes a reduction in the number of CD4+CD8+ thymocytes and mature medullary thymic epithelial cells (mTECs), accompanied by an increment in thymic epithelial cells (TECs) expressing both keratin-5 and keratin-8 (K5+K8+) that reportedly contain common TEC progenitors and mTEC progenitor [30,31,32]

  • T cell progenitors initially differentiate into CD4–CD8– (DN) cells and into CD4+CD8+ thymocytes (DP) in the thymus [14]

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Summary

Introduction

Spaceflight affects various immune systems [1,2,3]. Altered gravity is one of the hostile conditions during spaceflight, microgravity in orbit and high gravity force at launch and landing. Several studies on spaceflight missions suggested the impact of gravity change on immune systems [2, 3]. Due to the cost and limited availability of spaceflight missions, some ground-based models using experimental animals have been developed to test the effect of gravity changes on physiological parameters [4,5,6,7]. These ground studies have revealed the deleterious effect of gravity change on many immunological parameters

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