4.6 Article

Mapping Sphingolipid Metabolism Pathways during Phagosomal Maturation

期刊

ACS CHEMICAL BIOLOGY
卷 16, 期 12, 页码 2757-2765

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acschembio.1c00393

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资金

  1. DBT/Wellcome Trust India Alliance Fellowships [IA/I/15/2/502058, IA/S/11/2500255]
  2. Department of Science and Technology Fund for Improvement of S&T Infrastructure (DST-FIST) [SR/FST/LSII-043/2016]
  3. Department of Biotechnology

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This study elucidates the accumulation of ceramides during phagosomal maturation, highlighting the role of ceramide synthase 2 and the involvement of ceramidase activity. The findings indicate that lipid metabolism, especially the synthesis and metabolism of ceramides, plays a significant role in the process of phagocytosis and cellular detoxification.
Phagocytosis is an important physiological process, which, in higher organisms, is a means of fighting infections and clearing cellular debris. During phagocytosis, detrimental foreign particles (e.g. pathogens and apoptotic cells) are engulfed by phagocytes (e.g. macrophages), enclosed in membrane-bound vesides called phagosomes, and transported to the lysosome for eventual detoxification. During this well-choreographed process, the nascent phagosome (also called early phagosome, EP) undergoes a series of spatiotemporally regulated changes in its protein and lipid composition and matures into a late phagosome (LP), which subsequently fuses with the lysosomal membrane to form the phagolysosome. While several elegant proteomic studies have identified the role of unique proteins during phagosomal maturation, the corresponding lipidomic studies are sparse. Recently, we reported a comparative lipidomic analysis between EPs and LPs and showed that ceramides are enriched on the LPs. Further, we found that this ceramide accumulation on LPs was orchestrated by ceramide synthase 2, inhibition of which hampers phagosomal maturation. Following up on this study, here, using biochemical assays, we first show that the increased ceramidase activity on EPs also significantly contributes to the accumulation of ceramides on LPs. Next, leveraging lipidomics, we show that de novo ceramide synthesis does not significantly contribute to the ceramide accumulation on LPs, while concomitant to increased ceramides, glucosylceramides are substantially elevated on LPs. We validate this interesting finding using biochemical assays and show that LPs indeed have heightened glucosylceramide synthase activity. Taken together, our studies provide interesting insights and possible new roles of sphingolipid metabolism during phagosomal maturation.

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