Bioscience Chapter Database :: 3618 Chapters Now Online

Chapter category: Cell Metabolism

External Lysosomes The Osteoclast and its Unique Capacities to Degrade Mineralised Tissues

This chapter appears in the following book:

Lysosomes

Edited by: Paul Saftig
ISBN: 0-387-25562-1
» Get more information about this book at landesbioscience.com «

Chapter authors:
Vincent Everts, Wouter Beertsen


[+] view image
Lysosomes contain the enzymatic machinery to digest a host of organic substances. This degrading activity occurs primarily inside the living cell where the lysosomes reside. Yet, some cells use lysosomal enzymes in the extracellular space to digest proteins in their direct vicinity. Secretion of these enzymes by neutrophils is an essential step in the digestion/ killing of (parts of ) bacteria in the defence of an organism.1-4 Macrophages also may secrete lysosomal enzymes.2,5-7 Some observations even suggest that fibroblasts have the capacity to secrete such enzymes into the extracellular space.8,9 Since the majority of lysosomal enzymes are active at a low pH, an effective use of the enzymes extracellular can occur only if a low pH is created and maintained for some time. This is possible if the cell has the capacity to seclude a restricted area from its surrounding environment. The latter situation is highly effective during degradation of mineralised matrices, like bone and calcified cartilage. The cell primarily involved in this process is the multinucleated osteoclast.10,11 In the present paper some of the unique properties of this cell will be discussed, in particular its ability to create an extracellular lysosomal compartment, the prime site where resorption of mineralised tissue occurs.

» Access chapter for $19



Additional chapters from this book:

Transport of Lysosomal Enzymes

Stephan Storch and Thomas Braulke

More than 50 acid hydrolases involved in the ordered lysosomal degradation of a variety of proteins, lipids, carbohydrates, and nucleic acids have been identified. The hydrolases are enclosed by a m...

Adaptor Proteins in Lysosomal Biogenesis

P. Schu

Lysosomal membrane proteins and soluble lysosomal proteins are transported from the trans-Golgi network (TGN) to endosomes and lysosomes via coated-vesicles, which bud from the donor compartment and...

Papillomavirus Infections and Cancerogenesis of Squamous Cell and Basal Cell Carcinomas

Guido Bens

Human papillomaviruses (HPVs) are a large group of infectious agents that induce various lesions of skin and mucosae. The carcinogenic role of HPV types 16 and 18, mediated by inactivation of the tu...

Lysosomal Storage Disorders

Ole Kristian Greiner-Tollersrud and Thomas Berg

The lysosomal storage disorders (LSD) are a group of about 50 diseases that are characterised by an accumulation of waste products in the lysosomes, resulting in the formation of large intracellular...

History and Morphology of the Lysosome

Renate Lullmann-Rauch

The lysosome is the cell‘s main digestive compartment to which all sorts of macromol ecules are delivered for degradation. The structure of the lysosome is variable and de pends on the cell type and...

Lysosomal Proteases: Revival of the Sleeping Beauty

Klaudia Brix

Lysosomal proteases belong to the aspartic, cysteine, or serine proteinase families of hydrolytic enzymes. They are expressed ubiquitously, and in a tissue- or cell type-specific manner. Although we...

Lysosomal Membrane Proteins

Paul Saftig

The lysosomal limiting membrane has multiple functions including acidification of the lysosomal matrix, sequestration of lysosomal enzymes, mediation of fusion events beween lysosomes and other orga...

External Lysosomes The Osteoclast and its Unique Capacities to Degrade Mineralised Tissues

Vincent Everts, Wouter Beertsen

Lysosomes contain the enzymatic machinery to digest a host of organic substances. This degrading activity occurs primarily inside the living cell where the lysosomes reside. Yet, some cells use lyso...

Lysosomal Proteome and Transcriptome

Jobst Landgrebe and Torben Lübke

As reflected in this monograph, a lot of knowledge about the lysosomal compartment has been acquired since the discovery of the organelle by de Duve and others in the 1950s. Nevertheless, a lot of q...

Chaperone-Mediated Autophagy

Erwin Knecht* and Natalia Salvador

Many lysosomal and nonlysosomal pathways degrade intracellular proteins and this variety allows all cell proteins to be proteolysed at various speeds in response to different stimuli. Lysosomes, whi...

Membrane Resealing Mediated by Lysosomal Exocytosis

Norma W. Andrews

Ca2+-regulated exocytosis was proposed to mediate plasma membrane repair , but until recently the nature of the vesicles involved was unknown. Recent work from our labo ratory identified lysosomes a...

Neuronal Ceroid-Lipofuscinoses

Jaana Tyynela

Neuronal ceroid-lipofuscinoses (NCLs, also referred to as Batten’s disease) are inherited lysosomal storage diseases characterized by progressive neurodegeneration and premature death. As a group, t...

Therapy of Lysosomal Storage Diseases

Ulrich Matzner

Lysosomes are membrane-surrounded organelles which are present virtually in all animal cells. They function to degrade both intra- and extracellular macromolecules to low molecular components that a...

Macroautophagy in Mammalian Cells

Eeva-Liisa Eskelinen

Autophagy is a lysosomal degradation pathway for cytoplasmic material, which is activated during stress conditions such as amino acid starvation or viral infection. Yeast mutants defective in autoph...


SIGN IN

Email:


Password:


lost password?




[ Home | Authors | Editors | Custom Books | Chapter Reprints | Subscribe | Contact | Biotoons ]