Crucian Brian E, Quiriarte Heather, Lam Chiu-Wing, Nelman Mayra, Colorado Audrie A, Diak Douglass M, James John T
Environmental Sciences Branch, NASA Johnson Space Center, Houston, TX, United States.
School of Kinesiology, Louisiana State University, Baton Rouge, LA, United States.
Front Immunol. 2025 Feb 6;16:1538421. doi: 10.3389/fimmu.2025.1538421. eCollection 2025.
Due to cosmic radiation bombardment and over 4 billion meteorite and micrometeoroid impacts on the airless Moon, the lunar surface is covered by a layer of fine, reactive dust. Very little is known regarding the toxicity of lunar dust on human physiology. This study assessed airborne lunar dust exposure in rats on localized pulmonary and systemic immune parameters.
Rats were exposed to 0 (air only), 20.8 (low), and 60.6 (high) mg/m of respirable-size lunar dust for 4 weeks (6 h/day, 5 days/week). Rats were then euthanized either 1 day, 7 days, 4 weeks, or 13 weeks after the last exposure. Peripheral blood and lung lavage fluid samples were collected for analysis. Assays included leukocyte distribution by multicolor flow cytometry and electron/fluorescent microscopy to visualize cell-particulate interactions and lavage/plasma cytokine concentration. Mitogen-stimulated cytokine production profiles, as a measure of cellular function, were performed on whole blood samples only.
Untreated lavage fluid was comprised primarily of pulmonary macrophages. High-dose lunar dust inhalation (60.6 mg/m) resulted in an influx of both neutrophils and lymphocytes. Although the percentage of lymphocytes increased, the T-cell CD4:CD8 ratio was unchanged. Cytokine analysis of the lavage fluid showed increased levels of IL-1β and TNFα. These alterations generally persisted through the 13-week sampling. Blood analysis showed few systemic immune alterations from the lunar dust inhalation. By week 4, the peripheral granulocyte percentage was elevated in the treated rats. Plasma cytokine levels were unchanged in all treated rats compared to controls; however, altered mitogen-stimulated cytokine production profiles were observed consisting of increased IL-1β and IL-6 and decreased IL-2. There were minimal adverse immune effects, in both lung or peripheral blood, following low-dose exposure to 20.8 mg/m lunar dust.
Exposures to high concentrations of lunar dust resulted in persistent lung inflammation and some systemic immune dysregulation that did not subside even 13 weeks after the dust exposure. This information is beneficial in deriving an exposure limit to airborne lunar dust and for spacecraft engineers considering dust mitigation systems in lunar landers or habitats.
由于宇宙辐射轰击以及超过40亿次陨石和微流星体对无空气月球的撞击,月球表面覆盖着一层细小的、具有反应性的尘埃。关于月球尘埃对人体生理的毒性,人们了解甚少。本研究评估了大鼠吸入空气中月球尘埃后对局部肺部和全身免疫参数的影响。
将大鼠暴露于0(仅空气)、20.8(低剂量)和60.6(高剂量)mg/m³可吸入粒径的月球尘埃中4周(每天6小时,每周5天)。然后在最后一次暴露后的1天、7天、4周或13周对大鼠实施安乐死。采集外周血和肺灌洗液样本进行分析。检测包括通过多色流式细胞术分析白细胞分布,以及通过电子/荧光显微镜观察细胞与颗粒物的相互作用和灌洗液/血浆细胞因子浓度。仅对全血样本进行丝裂原刺激的细胞因子产生谱分析,以衡量细胞功能。
未处理的灌洗液主要由肺巨噬细胞组成。高剂量吸入月球尘埃(60.6 mg/m³)导致中性粒细胞和淋巴细胞流入。虽然淋巴细胞百分比增加,但T细胞CD4:CD8比值未变。灌洗液的细胞因子分析显示IL-1β和TNFα水平升高。这些改变通常在13周的采样期内持续存在。血液分析显示吸入月球尘埃后全身免疫改变较少。到第4周时,处理组大鼠外周粒细胞百分比升高。与对照组相比,所有处理组大鼠的血浆细胞因子水平均未改变;然而,观察到丝裂原刺激的细胞因子产生谱发生改变,包括IL-1β和IL-6增加以及IL-2减少。低剂量暴露于20.8 mg/m³月球尘埃后,肺部或外周血的不良免疫效应极小。
暴露于高浓度月球尘埃会导致持续的肺部炎症和一些全身免疫失调,即使在尘埃暴露13周后仍未消退。这些信息有助于确定空气中月球尘埃的暴露限值,并为考虑在月球着陆器或栖息地设置尘埃缓解系统的航天器工程师提供帮助。