Literature DB >> 12048238

Neuronal loss and brain atrophy in mice lacking cathepsins B and L.

Ute Felbor1, Benedikt Kessler, Walther Mothes, Hans H Goebel, Hidde L Ploegh, Roderick T Bronson, Bjorn R Olsen.   

Abstract

Cathepsins B and L are widely expressed cysteine proteases implicated in both intracellular proteolysis and extracellular matrix remodeling. However, specific roles remain to be validated in vivo. Here we show that combined deficiency of cathepsins B and L in mice is lethal during the second to fourth week of life. Cathepsin B(-/-)/L(-/-) mice reveal a degree of brain atrophy not previously seen in mice. This is because of massive apoptosis of select neurons in the cerebral cortex and the cerebellar Purkinje and granule cell layers. Neurodegeneration is accompanied by pronounced reactive astrocytosis and is preceded by an accumulation of ultrastructurally and biochemically unique lysosomal bodies in large cortical neurons and by axonal enlargements. Our data demonstrate a pivotal role for cathepsins B and L in maintenance of the central nervous system.

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Year:  2002        PMID: 12048238      PMCID: PMC122989          DOI: 10.1073/pnas.112632299

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  41 in total

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6.  A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration.

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7.  Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency.

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Review 7.  Cathepsin deficiency as a model for neuronal ceroid lipofuscinoses.

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10.  Cathepsin L inactivates human trypsinogen, whereas cathepsin L-deletion reduces the severity of pancreatitis in mice.

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