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Frequently, the indigestible remnants of lysosomal degradation remain in the cell, enclosed in vesicles referred to as residual bodies.

The lysosomal membrane maintains its integrity possibly because the luminal aspects of the membrane proteins are glycosylated to a much greater extent than those of other membranes thus preventing the degradation of the membrane.

Peroxisomes

Peroxisomes are membrane-bounded organelles housing oxidative enzymes such as urate oxidase, D-amino acid oxidase, and catalase. These organelles function

in the formation of free radicals (e.g., superoxides), which destroy various substances, and

in the protection of the cell by degrading hydrogen peroxide by catalase.

They also function in detoxification of certain toxins and in elongation of some fatty acids during lipid synthesis.

Most of the proteins intended for inclusions into peroxisomes are synthesized in the cytosol rather than on the RER. All peroxisomes are formed by fission from preexisting peroxisomes.

Proteasomes

Proteasomes are small, barrel-shaped organelles that function in the degradation of cytosolic proteins. There are two types of proteasomes, the larger 26S and the smaller 20S. The practice of cytosolic proteolysis is

THE CELL

7

highly regulated, and the candidate protein must be tagged by several ubiquitin molecules before it is permitted to be destroyed by the 26S proteasome system. The 20S proteasome degrades proteins that are oxidized by reactive oxygen species to form protein carbonyls.

Cytoskeleton

The cytoskeleton is composed of a filamentous array of proteins that act not only as the structural framework of the cell but also to transport material within it from one region of the cell to another and provide it with the capability of motion and cell division. Components of the cytoskeleton include

microtubules (consisting of a- and b-tubulins arranged in 13 protofilaments),

thin (actin) filaments (also known as microfilaments). Thin filaments function in the movement of cells from one place to another as well as in the movement of regions of the cell with respect to itself.

Intermediate filaments are thicker than thin and thinner than thick filaments. They function in providing a structural framework to the cell and resisting mechanical stresses placed on cells (Table 1-3).

Thick filaments, included here although not traditionally considered to be part of the cytoskeleton, are composed of myosin, and they interact with thin filaments to facilitate cell movement either along a surface or movement of cellular regions with respect to the cell.

TABLE 1-3Major Intermediate Filaments

Type

Location

Function

 

 

 

Keratin

Epithelial cells

Support; tension bearing; withstands stretching; associated

 

Cells of hair and nails

with desmosomes, hemidesmosomes, and tonofila-

 

 

ments; immunological marker for epithelial tumors

 

 

 

Vimentin

Mesenchymal cells, chondroblasts,

Structural support, forms cage-like structure around nucle-

 

fibroblasts, endothelial cells

us; immunological marker for mesenchymal cell tumors

 

 

 

Desmin and vimentin

Muscle: skeletal, smooth, cardiac

Links myofibrils to myofilaments; desmin is an immuno-

 

 

logical marker for tumors arising in muscle.

 

 

 

GFAP* and vimentin

Astrocytes, oligodendrocytes,

Support; GFAP is an immunological marker for glial tumors.

 

Schwann cells, and neurons

 

 

 

 

Neurofilaments

Neurons

Support of axons and dendrites, immunological marker for

 

 

neurological tumors

 

 

 

Lamins A, B, and C

Lines nuclear envelopes of all cells

Organizes and assembles nuclear envelope, maintains

 

 

organization of nuclear chromatin

*GFAP, glial fibrillar acidic protein