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Related Concept Videos

Phosphoinositides and PIPs01:42

Phosphoinositides and PIPs

Phosphoinositides are a group of phospholipids containing a glycerol backbone with two fatty acid chains and a phosphate attached to a myoinositol sugar ring. The inositol head group extends into the cytoplasm, where it is modified by adding phosphate groups to form phosphatidylinositol phosphates or PIPs.
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
IP3/DAG Signaling Pathway01:11

IP3/DAG Signaling Pathway

Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and produces two-second...
Synthesis of Phosphatidylcholine in the ER Membrane01:27

Synthesis of Phosphatidylcholine in the ER Membrane

The ER synthesizes lipids for building cell membranes and performing cellular functions such as energy storage and signaling. The lipid synthesis machinery embedded in the ER membrane primarily collects all reactants from the cytosol. Following synthesis, the secretory pathway and the ER contact sites distribute these lipids to other cellular organelles. Additionally, the energy-rich triacylglycerides are transported from the ER via lipid droplets.
The major components of all eukaryotic cell...
Asymmetric Lipid Bilayer01:35

Asymmetric Lipid Bilayer

Biological membranes show uneven distribution of different types of lipids in the inner and outer layers, resulting in transverse asymmetric membranes. The treatment of the erythrocyte membrane with the enzyme phospholipase confirmed the asymmetric nature of the lipid bilayer. The enzyme hydrolyzes lipids into fatty acids and hydrophilic groups. The phospholipase acts only on the outer layer of the membrane, while the inner layer remains intact. The phospholipase treatment resulted in 80%...
Overview of Fatty Acid Metabolism01:28

Overview of Fatty Acid Metabolism

Lipids also are sources of energy that power cellular processes. Like carbohydrates, lipids are composed of carbon, hydrogen, and oxygen, but these atoms are arranged differently. Most lipids are nonpolar and hydrophobic. Major types include fats and oils, waxes, phospholipids, and steroids.
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Lipid Digestion01:06

Lipid Digestion

Lipids are large molecules that are generally not water-soluble. Since most of the digestive enzymes in the human body are water-based, there are specific steps the body must take to break down lipids and make them available for use.

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A Liposome Membrane Permeability Assay for Investigating the Effects of Phosphatidylinositol Phosphate Groups on Membranotropic Action of Venom PLA2
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Secreted phospholipase A2 revisited.

Makoto Murakami1, Yoshitaka Taketomi, Hiroyasu Sato

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Secreted phospholipase A(2) (sPLA(2)) enzymes, once obscure, are now understood for their specific roles in pathophysiology. Recent research clarifies their expression, function, and extracellular actions.

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Area of Science:

  • Biochemistry
  • Enzymology
  • Molecular Biology

Background:

  • Phospholipase A(2) (PLA(2)) enzymes hydrolyze glycerophospholipids at the sn-2 position.
  • Mammals possess over 30 PLA(2) enzymes, including the secreted PLA(2) (sPLA(2)) family.
  • sPLA(2)s are low molecular weight, Ca(2+)-dependent enzymes with distinct localizations and functions.

Purpose of the Study:

  • To review recent advances in PLA(2) research, focusing on sPLA(2)s.
  • To elucidate the physiological functions and modes of action of sPLA(2)s.
  • To highlight extracellular phospholipid targets and lipid mediator production by sPLA(2)s.

Main Methods:

  • Studies utilizing knockout and transgenic mice.
  • Application of specific PLA(2) inhibitors.
  • Lipidomics analysis for isoform expression and function.

Main Results:

  • Clarification of sPLA(2) isoform expression patterns in vivo.
  • Identification of sPLA(2) involvement in specific pathophysiological conditions.
  • Understanding of sPLA(2) mechanisms in extracellular environments.

Conclusions:

  • The biological roles of sPLA(2)s in vivo are increasingly understood.
  • sPLA(2)s exhibit specialized functions in various pathophysiological contexts.
  • Research has advanced our knowledge of sPLA(2)s' extracellular targets and mediator production.