Title : Characterization of the intracellular proteolytic cleavage of
myocilin and identification of
calpain II as a
myocilin-processing
protease
Abstract :
- MYOC , a gene involved in different types of glaucoma, encodes myocilin , a secreted glycoprotein of unknown function, consisting of an N-terminal leucine-zipper-like domain , a central linker region , and a C-terminal olfactomedin-like domain
- Recently, we have shown that myocilin undergoes an intracellular endoproteolytic processing
- We show herein that the proteolytic cleavage in the linker region splits the two terminal domains
- The C-terminal domain is secreted to the culture medium, whereas the N-terminal domain mainly remains intracellularly retained
- In transiently transfected 293T cells, the cleavage was prevented by calpain inhibitors, such as calpeptin , calpain inhibitor IV, and calpastatin
- Since calpains are calcium-activated proteases, we analyzed how changes in either intra- or extracellular calcium affected the cleavage of myocilin
- Intracellular ionomycin-induced calcium uptake enhanced myocilin cleavage, whereas chelation of extracellular calcium by EGTA inhibited the proteolytic processing
- Calpains I and II cleaved myocilin in vitro
- However, in cells in culture, only RNA interference knockdown of calpain II reduced myocilin processing
- Subcellular fractionation and digestion of the obtained fractions with proteinase K showed that full-length myocilin resides in the lumen of the endoplasmic reticulum together with a subpopulation of calpain II
- These data revealed that calpain II is responsible for the intracellular processing of myocilin in the lumen of the endoplasmic reticulum
- We propose that this cleavage might regulate extracellular interactions of myocilin , contributing to the control of intraocular pressure
Output (sent_index, trigger,
protein,
sugar,
site):
- 1. glycoprotein, , glycoprotein, -, -
- 1. glycoprotein, , myocilin, -, -
Output(Part-Of) (sent_index,
protein,
site):
*Output_Site_Fusion* (sent_index,
protein,
sugar,
site):