Infographic: Piecing the Cholesterol Puzzle

How a rare disease led to an understanding of the basics of cholesterol regulation.

Diana Kwon
Diana Kwon

Diana is a freelance science journalist who covers the life sciences, health, and academic life. She’s a regular contributor to The Scientist and her work has appeared in several other...

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Apr 30, 2018

See larger version: PDF© CATHERINE DELPHIA

Research into familial hypercholesterolemia (FH), a rare disease in which the body is unable to rid itself of excess low-density lipoproteins (LDLs), provided fundamental insights into cholesterol metabolism. In 1974, geneticist Michael Brown and biochemist Joseph Goldstein reported that LDLs are less likely to bind to cells from FH patients than to cells from healthy individuals. This provided the first evidence that LDL receptors existed on the cell surface and set the stage for later work by Goldstein, Brown, and their colleagues to describe the ways that cholesterol derived from LDL helps regulate the production of the fatty molecule within the cell.

LDL receptors are first synthesized in the endoplasmic reticulum (1). After maturing in the Golgi apparatus, the receptors are transported in vesicles to the cell membrane (2). Once an LDL molecule has bound to the receptor (3), the complex is...

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Infographic: Piecing the Cholesterol Puzzle

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