Espejo Luis S, DeNicola Destiny, Chang Leah M, Hofschneider Vanessa, Haskins Anne E, Balsa Jonah, Freitas Samuel S, Antenor Angelo, Hamming Sage, Hull Bradford, Castro-Portuguez Raul, Dang Hope, Sutphin George L
Molecular & Cellular Biology, University of Arizona, Tucson, AZ, USA.
bioRxiv. 2024 Jan 9:2024.01.07.574394. doi: 10.1101/2024.01.07.574394.
3-hydroxyanthranilic acid (3HAA) is considered to be a fleeting metabolic intermediate along tryptophan catabolism through the kynurenine pathway. 3HAA and the rest of the kynurenine pathway have been linked to immune response in mammals yet whether it is detrimental or advantageous is a point of contention. Recently we have shown that accumulation of this metabolite, either through supplementation or prevention of its degradation, extends healthy lifespan in and mice, while the mechanism remained unknown. Utilizing as a model we investigate how 3HAA and inhibition impact the host and the potential pathogens. What we find is that 3HAA improves host immune function with aging and serves as an antimicrobial against gram-negative bacteria. Regulation of 3HAA's antimicrobial activity is accomplished via tissue separation. 3HAA is synthesized in the hypodermal tissue, localized to the site of pathogen interaction within the gut granules, and degraded in the neuronal cells. This tissue separation creates a new possible function for 3HAA that may give insight to a larger evolutionarily conserved function within the immune response.
3-羟基邻氨基苯甲酸(3HAA)被认为是色氨酸通过犬尿氨酸途径分解代谢过程中的一种短暂代谢中间体。3HAA和犬尿氨酸途径的其他部分与哺乳动物的免疫反应有关,但它是有害还是有益仍存在争议。最近我们发现,通过补充这种代谢物或阻止其降解,该代谢物的积累可延长线虫和小鼠的健康寿命,但其机制尚不清楚。利用线虫作为模型,我们研究了3HAA和其抑制作用如何影响宿主和潜在病原体。我们发现,3HAA随着衰老改善宿主免疫功能,并作为一种抗革兰氏阴性菌的抗菌剂。3HAA抗菌活性的调节是通过组织分隔来实现的。3HAA在皮下组织中合成,定位于肠道颗粒内病原体相互作用的部位,并在神经细胞中降解。这种组织分隔为3HAA创造了一种新的可能功能,这可能有助于深入了解免疫反应中一个更大的进化保守功能。