Histiocyte Explained

Histiocyte
Latin:macrophagocytus immobilis
System:Immune system

A histiocyte is a vertebrate cell that is part of the mononuclear phagocyte system (also known as the reticuloendothelial system or lymphoreticular system). The mononuclear phagocytic system is part of the organism's immune system. The histiocyte is a tissue macrophage[1] or a dendritic cell[2] (histio, diminutive of histo, meaning tissue, and cyte, meaning cell). Part of their job is to clear out neutrophils once they've reached the end of their lifespan.

Development

Histiocytes are derived from the bone marrow by multiplication from a stem cell. The derived cells migrate from the bone marrow to the blood as monocytes. They circulate through the body and enter various organs, where they undergo differentiation into histiocytes, which are part of the mononuclear phagocytic system (MPS).

However, the term histiocyte has been used for multiple purposes in the past, and some cells called "histocytes" do not appear to derive from monocytic-macrophage lines.[3] The term Histiocyte can also simply refer to a cell from monocyte origin outside the blood system, such as in a tissue (as in rheumatoid arthritis as palisading histiocytes surrounding fibrinoid necrosis of rheumatoid nodules).

Some sources consider Langerhans cell derivatives to be histiocytes.[4] The Langerhans cell histiocytosis embeds this interpretation into its name.

Structure

Histiocytes have common histological and immunophenotypical characteristics (demonstrated by immunostains). Their cytoplasm is eosinophilic and contains variable amounts of lysosomes. They bear membrane receptors for opsonins, such as IgG and the fragment C3b of complement. They express LCAs (leucocyte common antigens) CD45, CD14, CD33, and CD4 (also expressed by T helper cells).

Macrophages and dendritic cells

These histiocytes are part of the immune system by way of two distinct functions: phagocytosis and antigen presentation. Phagocytosis is the main process of macrophages and antigen presentation the main property of dendritic cells (so called because of their star-like cytoplasmic processes).

Macrophages and dendritic cells are derived from common bone marrow precursor cells that have undergone different differentiation (as histiocytes) under the influence of various environmental (tissue location) and growth factors such as GM-CSF, TNF and IL-4. The various categories of histiocytes are distinguishable by their morphology, phenotype, and size.

Langerhans cells

A subset of cells differentiates into Langerhans cells; this maturation occurs in the squamous epithelium, lymph nodes, spleen, and bronchiolar epithelium. Langerhans cells are antigen-presenting cells but have undergone further differentiation. Skin Langerhans cells express CD1a, as do cortical thymocytes (cells of the cortex of the thymus gland). They also express S-100, and their cytoplasm contains tennis-racket like ultra-structural inclusions called Birbeck granules.

Clinical significance

Histiocytoses describe neoplasias wherein the proliferative cell is the histiocyte. The most common histiocyte disorders are Langerhans' cell histiocytosis and haemophagocytic lymphohistiocytosis.[5]

See also

Notes and References

  1. Cline . Mj . Histiocytes and histiocytosis. Blood . 1 November 1994 . 84 . 9 . 2840–2853 . 10.1182/blood.V84.9.2840.2840 . free .
  2. Chorro L, Geissmann F . Development and homeostasis of 'resident' myeloid cells: the case of the Langerhans cell . Trends in Immunology . 31 . 12 . 438–45 . December 2010 . 21030305 . 10.1016/j.it.2010.09.003 .
  3. Web site: S12C3-Granuloma . 2009-01-06 . 2009-09-29 . https://web.archive.org/web/20090929083449/http://www.som.tulane.edu/classware/pathology/medical_pathology/InflamDermato/S12C3Granuloma/s12c3granuloma.htm . dead .
  4. Cline MJ . Histiocytes and histiocytosis . Blood . 84 . 9 . 2840–53 . November 1994 . 10.1182/blood.V84.9.2840.2840 . 7524755 . free .
  5. Webb DK . Histiocyte disorders . British Medical Bulletin . 52 . 4 . 818–25 . October 1996 . 9039734 . 10.1093/oxfordjournals.bmb.a011585 . free .