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A rare autosomal disorder, neutral lipid storage disease, is characterized by the accumulation of excess neutral lipids in multiple tissues and is associated with mutations in ATGL and CGI-58 genes that are involved in lipolysis [143]

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While the molecular details governing cross-talk between the two PLA 2 s remain to be fully clarified, it has been shown that sPLA 2 -V regulates cPLA 2 phosphorylation (132, 135)

[DOI] [Google Scholar] Chen G., Fan M., Liu Y., Sun B., Liu M., Wu J., Li N., Guo M