Page 27 - Veterinary Histology of Domestic Mammals and Birds, 5th Edition
P. 27

The cell (cellula)  9




       VetBooks.ir



























                  1.8  Lysosome with adjacent lipid droplet in a liver cell
                  (x10,000).
                                                                 1.9  Lysosomes in the tubular epithelium of the kidney
                                                                 of a dog (x22,000).
                  Lysosomes (lysosoma)
                  Lysosomes are membrane-bound organelles responsible
                  for intracellular digestion and enzymatic degradation of
                  soluble and solid substances.
                     Lysosomes contain a large range of structurally diverse
                  enzymes (acid hydrolases). These are synthesised in the
                  rER and sorted in the Golgi apparatus. Depending on the
                  function of the cell, lysosomal enzymes consist primarily
                  of acid phosphatases, glycosidases, peptidases (proteases),
                  esterases, sulfatases, deoxyribonucleases and ribonucleases
                  (active at pH 5.0). The enzymes are separated from the
                  surrounding cytosol by a phosphatide-glycolipid-protein
                  membrane with a built-in proton-ATPase (proton pump).
                     Lysosomal enzymes are responsible for the digestion
                  of substances originating from inside and outside the
                  cell. The end products (nucleotides, amino acids or sugars)
                  pass into the cell matrix where they are incorporated into
                  cellular metabolic processes.
                     Material that cannot be digested enzymatically is
                  retained within the lysosome as residual bodies. These
                  may be ejected from the cell through the plasmalemma.   1.10  Lysosomes in a peritoneal macrophage (x4500).
                  Those that remain within the cell can lead to formation of
                  endogenous pigments (e.g. lipofuscin).
                     Lysosomes are also involved in physiological processes   Abnormalities of lysosomal enzyme function can give rise
                  associated with embryogenesis and play a role in pro-  to lysosomal storage diseases. These are characterised by
                  grammed cell death (apoptosis).                the genetically determined absence of functional enzymes,
                     Disruption of the integrity of the lysosomal mem-  resulting in accumulation of undigested substrates.
                  brane, by endogenous or exogenous factors, results in the
                  release of lysosomal enzymes into the surrounding cyto-  LYSOSOME STRUCTURE
                  sol, leading to degradation of cellular components within  Lysosomes are ovoid to spherical organelles (Figures 1.6
                  the cytoplasm. Causative factors include oxygen deficiency,  to 1.10). Their limiting membrane is reinforced by an
                  X- and UV radiation and various cytotoxins. This process,  abundance of glycolipids. The membrane permits egress
                  referred to as autolysis, usually results in death of the cell.  of metabolic end products into the cytosol and facilitates









       Vet Histology.indb   9                                                                                    16/07/2019   14:52
   22   23   24   25   26   27   28   29   30   31   32