Lymphopoiesis (lĭm'fō-poi-ē'sĭs) (or lymphocytopoiesis) is the generation of lymphocytes, one of the five types of white blood cells (WBCs). It is more formally known as lymphoid hematopoiesis. Disruption in lymphopoiesis can lead to a number of lymphoproliferative disorders, such as lymphomas and lymphoid leukemias.
Overview
Lymphocytes are blood cells of lymphoid (rather than the myeloid or erythroid) lineage. Lymphocytes are found in the bloodstream and originate in the bone marrow, however, they principally belong to the separate lymphatic system, which interacts with the blood circulation. Lymphopoiesis is now usually used interchangeably with the term "lymphocytopoiesis" – the making of lymphocytes, but some sources distinguish between the two, stating that "lymphopoiesis" additionally refers to creating lymphatic tissue, while "lymphocytopoiesis" refers only to the creation of cells in that tissue. The two classes of WBCs in mice originate from progenitor cells: myeloids from the common myeloid progenitor (CMP), and lymphoids from the common lymphoid progenitor (CLP).
In the case of mammals such as humans (Homo sapiens), lymphopoiesis begins with limited passive provision from the mother. This includes lymphocytes and immunoglobulin G that cross the placenta and enter the fetus to provide some protection against pathogens, as well as leukocytes that come from breast milk and enter circulation via the digestive tract. It is often not effective in preventing infections in the newborn. However, early in gestation, the developing embryo has begun its own lymphopoiesis from the fetal liver. Lymphopoiesis also arises from the yolk sac. This is in contrast to the adult where all lymphocytes originate in the bone marrow. There are four major types of lymphocytes, along with many sub-types.
Function Mature lymphocytes are a critical part of the immune system that, with the exception of memory B and T cells, have short lives measured in days or weeks and must be continuously generated throughout life by cell division and differentiation from cells such as common lymphoid progenitors (CLPs) in mice. The set comprising CLP cells and similar progenitors are themselves descendants of the pluripotential hemopoietic stem cell (pHSC), which is capable of generating all of the cell types of the complete blood cell system. Despite their ability to generate the complete suite of lymphocytes, most progenitors are not true stem cells, and must be continually renewed by differentiation from the pHSC stem cell. Many progenitor cells are also referred to as transit cells, sometimes also called transit amplifying cells, the meaning of this term being that the transit cell may find a new sub-lineage but the number of resultant cells is strictly limited (although possibly very large, even trillions yet finite) and the lineage is terminated by cells that die off (by apoptosis) or remain as cells that can no longer divide. Examples of such cells are CFUs (Colony-forming units – referred to as such because of their ability to form colonies in vitro in artificial media) such as CFU-T. Transplantation of a single pHSC cell can reconstitute a sub-lethally irradiated host (i.e. a mouse that has been irradiated so that all leukocytes are killed) with all these lineages of cells, including all types of lymphocytes via CLPs. Lymphopoiesis continues throughout life and so progenitor cells and their parent stem cells must always be present.
Process
Lymphopoiesis is a recursive process of cell division and also as a process of differentiation, measured by changes to the properties of cells. The function of lymphopoiesis is the production of various lymphocytes from common lymphoid progenitor (CLP) cells, which are in turn derived from hematopoietic stem cells.
Division and differentiation Given that lymphocytes arise from specific types of limited stem cells – which we can call P (for Progenitor) cells – such cells can divide in several ways. These are general principles of limited stem cells. Considering the P as the ‘mother’ cell, but not a true stem cell, it may divide into two new cells, which are themselves identical, but differ to some degree from the mother. Or the mother cell P may divide unequally into two new daughter cells both of which differ from each other and also from the mother. Any daughter cell will usually have new specialized abilities and if it is able to divide it will form a new sub-lineage. The difference of a daughter cell from the mother may be great, but it could also be much less, even subtle. What the P mother cell does not do is divide into two new P mother cells or a mother and a daughter; this is a matter of observation as such limited progenitor cells are known to not self-renew.
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