Cell Lines For Studying Phospholipases

What are Phospholipases?

Definition: Phospholipases are ubiquitously expressed enzymes that control the levels of phospholipid substrates by catalysing the lysis of phosphorylated lipids. The released lipid molecules then initiate signalling cascades known to regulate cell function.

This complex family is involved in the mechanisms of a number of diseases including cancer and heart disease, and has been implicated in conditions such as brain disorder/injury, kidney and immune cell dysfunction.

There are four distinct classes of phospholipases (PL), identified as PLA, PLB, PLC and PLD, each promoting cleavage at specific ester bonds within phospholipids. Each phospholipase family has several isoforms, which function within specific cell types and are differentially distributed.

The PLA class has members A1 and A2. PLA1 specifically hydrolyses the acyl group at the SN-1 position of phospholipids and both extracellular and intracellular PLA1 enzymes are known in mammals.

PLA2 cleaves the second carbon group of glycerol to release the fatty acid molecule, and includes both cytosolic and secreted phospholipases. PLA2is responsible for the release of arachidonic acid from membrane phospholipids. This leads to the formation of eicosanoids, including leukotrienes and prostaglandins, which can affect many potentially pathogenic responses, such as diverse inflammatory/allergic diseases. PLA2 isoforms have also been implicated in neurological disorders. PLA2G6 is involved in regulating levels of phosphatidylcholine and PLA2G6 mutations have been linked with infantile neuroaxonal dystrophy, a progressive neurological disorder that causes intellectual disability and movement problems.

PLB cleaves acyl chains from both the sn-1 and sn-2 positions, and so can carry out the reactions of both PLA1 and PLA2.

PLCs are only found intracellularly, and cleave phospholipids before the phosphate group, generating diacylglycerol, DAG, and inositol triphosphate (IP3). A wide range of disorders has been associated with PLC genetic aberrations. Mutations in PLCB1 have been linked to a form of epilepsy and changes in the PLCG2 gene are associated with auto-inflammation and antibody deficiency. The development of PLC inhibitors is an active area of research.

There are several isoforms of phospholipase D, and these play a central role in numerous physiological processes, including membrane traffickingcytoskeletal reorganization, receptor-mediated endocytosisexocytosis, and cell migration.  PLD isoforms has been implicated in the pathophysiology of multiple diseases, in particular the progression of Parkinson’s and Alzheimer’s (PLD3), and various cancers (PLD2). 

Examples of popular knockout cell lines





















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