TY - THES
T1 - Characterizing the effects of lunar dust simulants on T-cell viability and activation
AU - Ferreira da Silva Miranda, Silvana
A2 - Baatout, Sarah
A2 - Baselet, Bjorn
N1 - Score=N/A
PY - 2022/7/1
Y1 - 2022/7/1
N2 - With the Artemis Program, humans are returning to the Moon for the first time in 50 years.
During precedent Apollo missions, astronauts got into contact with lunar dust, and reported
visual obstruction, nose and throat irritation, skin irritation, dust pollution and psychological
effects which could be the result of lunar dust exposure (Cain, 2010; Cernan et al., 1973; Park
et al., 2008; Stubbs et al., 2007; Taylor et al., 2005). Lunar dust has been thoroughly examined
to describe its chemical and morphological characteristics and behaviour. Due to these
descriptions, lunar dust simulants (LDS) were developed to be able to perform research of
lunar dust (and LDS) on the human body. Prominent research has revealed the many adverse
effects lunar dust might have on the immune system, lungs, cardiovascular system, skin, eyes,
neurons and machinery. These studies are important to characterise these effects and for the
development of biological countermeasures as well as avoidance by technical
countermeasures. In this study, the effects of Lunar Highland Simulant (LHS-1) and Lunar
Mare Simulant (LMS-1), were examined on the viability and cytokine release in Jurkat cells.
By performing MTS assays and IL-2 ELISA assay. These assays encountered several
methodological issues and were first optimised to retain reliable results. LHS-1 and LMS-1,
induce cell death in Jurkat cells, up to 50%, independent of the LDS concentration. Exposure
to LMS-1 leads to an increased IL-2 release in Jurkat cells. When exposed to LHS-1, the IL-2
concentration is inversely proportional to the LHS-1 dose. This might be the result of cell death
caused by LHS-1 or the interaction of LHS-1 with IL-2. In addition, the LDS were visualised
with a scanning electron microscope (SEM) as well as the LDS exposed Jurkat cells. It could
be noticed how LDS particles cover the cell’s surface, indicating that the dust likely could
interfere with the cellular processes and mechanisms. LHS-1 and LMS-1 were characterised
by an SEM to test their compatibility with lunar dust. The LDS lack nanophase iron and the
vesicular surface of lunar dust which might play a critical role in its toxicity. Further research is
needed to test the effects of lunar dust, and in combination with other space stressors, on the
immune system further.
AB - With the Artemis Program, humans are returning to the Moon for the first time in 50 years.
During precedent Apollo missions, astronauts got into contact with lunar dust, and reported
visual obstruction, nose and throat irritation, skin irritation, dust pollution and psychological
effects which could be the result of lunar dust exposure (Cain, 2010; Cernan et al., 1973; Park
et al., 2008; Stubbs et al., 2007; Taylor et al., 2005). Lunar dust has been thoroughly examined
to describe its chemical and morphological characteristics and behaviour. Due to these
descriptions, lunar dust simulants (LDS) were developed to be able to perform research of
lunar dust (and LDS) on the human body. Prominent research has revealed the many adverse
effects lunar dust might have on the immune system, lungs, cardiovascular system, skin, eyes,
neurons and machinery. These studies are important to characterise these effects and for the
development of biological countermeasures as well as avoidance by technical
countermeasures. In this study, the effects of Lunar Highland Simulant (LHS-1) and Lunar
Mare Simulant (LMS-1), were examined on the viability and cytokine release in Jurkat cells.
By performing MTS assays and IL-2 ELISA assay. These assays encountered several
methodological issues and were first optimised to retain reliable results. LHS-1 and LMS-1,
induce cell death in Jurkat cells, up to 50%, independent of the LDS concentration. Exposure
to LMS-1 leads to an increased IL-2 release in Jurkat cells. When exposed to LHS-1, the IL-2
concentration is inversely proportional to the LHS-1 dose. This might be the result of cell death
caused by LHS-1 or the interaction of LHS-1 with IL-2. In addition, the LDS were visualised
with a scanning electron microscope (SEM) as well as the LDS exposed Jurkat cells. It could
be noticed how LDS particles cover the cell’s surface, indicating that the dust likely could
interfere with the cellular processes and mechanisms. LHS-1 and LMS-1 were characterised
by an SEM to test their compatibility with lunar dust. The LDS lack nanophase iron and the
vesicular surface of lunar dust which might play a critical role in its toxicity. Further research is
needed to test the effects of lunar dust, and in combination with other space stressors, on the
immune system further.
KW - Lunar dust toxicity
KW - Immune System
KW - Space biology
UR - https://ecm.sckcen.be/OTCS/llisapi.dll/open/49842971
M3 - Master's thesis
PB - KUL - Katholieke Universiteit Leuven
ER -