Anatomy, Blood Vascular System PDF

BLOOD-VASCULAR SYSTEM & LYMPHATIC SYSTEM BLOOD Blood is a unique form of connective tissue composed of a liquid extracellular matrix called blood plasma that dissolves and suspends various cells and cell fragments. Blood is denser and more viscous than water and fee...

BLOOD-VASCULAR SYSTEM & LYMPHATIC SYSTEM BLOOD Blood is a unique form of connective tissue composed of a liquid extracellular matrix called blood plasma that dissolves and suspends various cells and cell fragments. Blood is denser and more viscous than water and feels slightly sticky. The temperature of blood is 38oC (100.4oF), about 1oChigher than oral or rectal body temperature, and it has a slightly alkaline pH ranging from 7.35 to 7.45. The blood constitutes about 20% of extracellular fluid, amounting to 8% of the total body mass. The blood volume is 5 to 6 liters (1.5 gal) in an average-sized adult male and 4 to 5 liters (1.2 gal) in an average-sized adult female. In the body, blood is responsible for the: (a) Transportation of oxygen, carbon dioxide, nutrients, hormones, heat and wastes. (b) Regulation of pH, body temperature and water content of cells. (c) Protection against blood loss through clotting, and against disease through phagocytic white blood cells and antibodies. HEMATOPOIESIS A continuous, regulated process of blood cell production that includes cell renewal, proliferation, differentiation, and maturation. These processes result in the formation, development, and specialization of all of the functional blood cells that are released from the bone marrow to the circulation. Types: (1) Primitive hematopoiesis - blood cell production that occurs during the mesoblastic stage of development. (2) Definitive hematopoiesis- begins during the fetal liver stage and continuous through adult life. In adults, all of these processes are restricted primarily to the bone marrow. During fetal development, hematopoiesis occurs in different areas of the developing fetus. This process has been divided into three phases: a. Mesoblastic Phase (Yolk Sac Phase) Hematopoiesis is considered to begin around the 19thday of embryologic development after fertilization. Progenitor cells of mesenchymal origin migrate from the aorta-gonad-mesonephros region of the developing aorta-splanchnopleure to the yolk sac. The cells arising from the aorta-gonad-mesonephros region give rise to hematopoietic stem cells (HSCs), but not to primitive erythroblasts.  The primitive erythroblasts found in the yolk sac arise from mesodermal cells, which initially line the cavity of the yolk sac. These primitive cells migrate from the periphery into the central cavity of the yolk sac, where they develop into primitive erythroblasts. The remaining cells surrounding the cavity of the yolk sac are called angioblasts and form the future blood vessels. The yolk sac phase of hematopoiesis is characterized by the development of primitive erythroblasts that produce measurable amounts of hemoglobin, including: A. Portland B. Gower-1 C. Gower-2. Note: Yolk sac hematopoiesis does not contribute significantly to definitive hematopoiesis. This phase of hematopoiesis occurs intravascularly, or within a developing blood vessel. b. Hepatic Phase The hepatic phase of hematopoiesis begins at 4 to 5 gestational weeks and is characterized by recognizable clusters of developing erythroblasts, granulocytes, and monocytes. The developing erythroblasts signal the beginning of definitive hematopoiesis with a decline in primitive hematopoiesis of the yolk sac. In addition, lymphoid cells begin to appear. Hematopoiesis during this phase occurs extravascularly, with the liver remaining the major site of hematopoiesis during fetal life and retaining activity until 1 to 2 weeks after birth. Hematopoiesis in the aorta-gonad-mesonephros region and the yolk sac disappears during this stage. Hematopoiesis in the fetal liver reaches its peak by the third month of development. The developing spleen, kidney, thymus, and lymph nodes contribute to the hematopoietic process during this phase. The thymus, the first fully developed organ in the fetus becomes the major site of T-cell production, whereas the kidneys and spleen produce B cells. Production of megakaryocytes also begins during the hepatic phase. The spleen gradually decreases granulocytic production and involves itself solely in lymphopoiesis. During the hepatic phase, detectable levels of hemoglobin (Hb) F,n Hb A, and Hb A2 may be present. c. Medullary (Myeloid) Phase During the fifth month of fetal development, hematopoiesis begins in the developing bone marrow cavity. This transition is called medullary hematopoiesis because it occurs in the medulla or inner part of the bone marrow. During this phase, mesenchymal cells, which are a type of embryonic tissue, migrate into the core of the bone and differentiate into skeletal and hematopoietic blood cells. Hematopoietic activity, especially myeloid activity, is apparent during this stage of development, and the myeloid-to-erythroid ratio approaches the adult level of 3:1 by 21 weeks of gestation.  By the end of the sixth month, the bone marrow becomes the primary site of hematopoiesis. Measurable levels of erythropoietin (EPO), granulocyte colony-stimulating factor (G-CSF), granulocyte-monocyte colony-stimulating factor (CM-GSF), fetal hemoglobin, Hb A2, and adult hemoglobin can be detected. In addition, cells at various stages of maturation can be seen in all three lineages. In adults, hematopoietic tissue is involved in the proliferation and maturation of blood cells. Numerous organs and tissues contribute to this process, including the bone marrow, lymph nodes, spleen, liver, and thymus. The bone marrow contains developing erythroid, myeloid, megakaryocytic and lymphoid cells. The tissues where lymphoid development occurs are divided into: 1. Primary lymphoid tissue - consists of the bone marrow and thymus and is where T and B cells are derived. 2. Secondary lymphoid tissue - where lymphoid cells become competent, consists of the spleen and lymph nodes and gut-associated lymphoid tissue. a. Bone Marrow Bone marrow, one of the largest organs in the body, is defined as the tissue located within the cavities of the cortical bones. These cavities consist of trabecular bone resembling a honeycomb. Normal bone marrow located within these cavities consists of two types of marrow: a. Red marrow - hematopoietically active marrow - Red marrow in adults is found in the sternum, skull, scapulae, vertebrae, ribs, pelvic bones, and proximal ends of the long bones. b. Yellow marrow - Represents the hematopoietically inactive marrow composed primarily of adipocytes (fat cells). Note: Normal adult bone marrow has approximately equal amounts of red and yellow marrow. A central space is created within the cavities of these bones by resorption of cartilage and endosteal bone. Mesenchymal cells migrate into the space and eventually differentiate into three cell types, which give rise to the blood and bone marrow matrix cells (reticular cells and adipose tissue). Reticular cells are formed on the exterior surfaces of the venous sinuses and extend long, narrow branches into the perivascular space, creating a meshlike network; this provides a supportive skeletal network for developing hematopoietic cells, macrophages and mast cells. During infancy and early childhood, the bone marrow consists primarily of red active marrow. Between 5 and 7 years of age, adipocytes become more abundant and begin to occupy the spaces in the long bones previously dominated by active marrow.  The process of replacing the active marrow by adipose tissue (yellow marrow) during development is called retrogression and eventually results in restriction of the active marrow to the flat bones: a. sternum b. vertebrae c. pelvis d. ribs e. skull f. proximal portion of the long bones. Areas located within the bone marrow cavity where red marrow has been replaced by yellow marrow consist of a mixture of adipocytes, undifferentiated mesenchymal cells, and macrophages. Inactive yellow marrow is also scattered throughout active red marrow and is capable of reverting back to active marrow in cases of increased demand on the bone marrow. Such cases might be excessive blood loss or increased erythrocyte destruction in the bone marrow by toxic chemicals or irradiation. Red Marrow The red marow is composed of extravascular cords that contain all of the developing blood cell lineages, stem and progenitor cells, adventitial cells, and macrophages. The cords are separated from the lumen of the sinusoids by endothelial and adventitial cells and are located between the trabeculae of spongy bone. Trabeculae are projections of calcified bone radiating out from the cortical bone into the marrow space and provide support for the developing marrow. The hematopoietic cells tend to develop in specific niches within the cords. Normoblasts develop in small clusters adjacent to the outer surfaces of the vascular sinuses; in addition, some normoblasts are found surrounding iron-laden macrophages. Megakaryocytes are located close to the vascular walls of the sinuses, which facilitates the release of platelets into the lumen of the sinusoids. Immature myeloid (granulocytic) cells through the metamyelocyte stage are located deep within the cords. As these maturing granulocytes proceed along their differentiation pathway, they move closer to the vascular sinuses. The mature blood cells of the bone marrow eventually enter the peripheral circulation by a process that is not well understood. Through a highly complex interaction between the maturing blood cells and the sinus wall, blood cells pass between layer of adventitial cells that form a discontinuous along the luminal side of the bone marrow sinus. Adjacent to the layer of adventitial cells is a basement membrane followed by continuous layer of endothelial cells on the luminal side of the bone marrow sinus. These adventitial cells are described as reticular cells and extend long cytoplasmic processes into the marrow cords.  The extensions of these reticular filaments form a meshwork that provides support for the developing hematopoietic cells. The adventitial cells are capable of contacting, which allows mature blood cells to pass through basement membrane and interact with the endothelial layer. As blood cells come in contact with endothelial cells, they bind to the surface via a receptor-mediated process. Cells pass through pores in the endothelial cytoplasm and are released into the circulation. Marrow Circulation The nutrient and gas requirements of the marrow are supplied by the nutrient and periosteal arteries, which enter via the bone foramina. The nutrient artery supplies blood only to the marrow. It coils around the central longitudinal vein, which passes along the bone canal. In the marrow cavity, the nutrient artery divides into ascending and descending branches that also coil around the central longitudinal vein.  The arteriole branches that enter the inner lining of the cortical bone (endosteum) form sinusoids (endosteal beds), which connect to periosteal capillaries that extend from the periosteal artery. The periosteal arteries provide nutrients for the osseous bone and the marrow. Their capillaries connect to the venous sinuses located in the endosteal bed, which empty into a larger collecting sinus that opens into the central longitudinal vein. Blood exits the marrow via the central longitudinal vein, which runs the length of the marrow. The central longitudinal vein exits the marrow through the same foramen where the nutrient artery enters. Hematopoietic cells located in the endosteal bed receive the nutrients from the nutrient artery. Hematopoietic Microenvironment The hematopoietic inductive microenvironment plays an important role in stem cell differentiation and proliferation. It is responsible for supplying a semifluid matrix, which serves as an anchor for the developing hematopoietic cells. The matrix is responsible for maintaining differentiation and proliferation and provides a supporting tissue in the hematopoietic inductive microenvironment. Stromal cells in the matrix are of several types: a. endothelial cells b. adipocytes c. macrophages d. osteoblasts e. osteoclasts f. reticular cells (fibroblasts). Endothelial cells - are broad flat cells that form a single continuous layer along the inner surface of the bone marrow sinus. - they regulate the flow of particles entering and leaving hematopoietic spaces. Adipocytes - are large cells with a single fat vacuole; they secrete various steroids that influence erythropoiesis and maintain bone integrity. - they also play a role in regulating the volume of the marrow in which active hematopoiesis occurs. Macrophages - function in phagocytosis and secretion of various cytokines that regulate hematopoiesis and are located throughout the marrow space. Osteoblasts- are bone-forming cells, and osteoclasts are bone-resorbing cells. Reticular cells - are associated with the formation of reticular fibers that form a lattice that supports the vascular sinuses and developing hematopoietic cells. Stromal cells - are believed to be derived from fibroblasts. - they play a role in support and regulation of hematopoietic stem progenitor cell survival and differentiation. The extracellular matrix of the bone marrow - contains proteoglycans or glycosaminoglycans, fibronectin, collagen, laminin, hemonectin, and thrombospondin. - Proteoglycans are expressed on the endothelial cell surface and mediate progenitor binding to the stroma. - Fibronectin, collagen, laminin, hemonectin, and thrombospondin function as adhesion molecules, promoting the adhesion of HSCs to the extracellular matrix. b. Liver The liver plays a significant role in hematopoiesis beginning around the second trimester and serves as the major site of blood cell production during the hepatic stage of hematopoiesis. In adults, the liver has many cellular production functions, including synthesizing various transport proteins storing essential minerals and vitamins that are used in the synthesis of deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), conjugating bilirubin from hemoglobin degradation and transporting bilirubin to the small intestine for eventual excretion. The liver consists of two lobes situated beneath the diaphragm in the abdominal cavity. The position of the liver with regard to the circulatory system is optimal for gathering transferring and eliminating substances via the bile. Anatomically liver cells are arranged in radiating hepatic lobules emanating from a central vein. Adjacent to the longitudinal lobes of the liver and separated only by a small space are sinusoids, which are lined by two types of cells Kupffer cells and epithelial cells. Kupffer cells are macrophages, removing cellular and foreign debris from the blood that circulates through the liver; they also are responsible for protein synthesis. The epithelial cells are arranged in the lining so as to be separated from one another by a noncellular area; this arrangement allows plasma to have direct access to the hepatocytes. This unusual organization of the liver and its location in the body enables it to be involved in many varied functions. Liver Pathophysiology The liver is often involved in blood-related diseases. In porphyrias, the liver exhibits enzymatic deficiencies that result in the accumulation of the various intermediary porphyrias. In severe hemolytic anemias and red blood cell (RBC) dysplasias, the conjugation of bilirubin and the storage of iron are increased. The liver sequesters membrane-damaged RBCs and rernoves them from the circulation. The liver is capable extramedullary hematopoietic production in case of bone marrow shutdown.  It is directly affected by storage diseases of the monocyte/macrophage (Kupffer) cells as a result of enzymatic deficiencies that cause hepatomegaly with ultimate dysfunction of the liver (Gaucher disease, Niemann-Pick disease, Tay-sachs disease. c. Spleen The spleen is the largest lymphoid organ in the body. The spleen is located directly beneath the diaphragm behind the fundus of the stomach in the upper left quadrant of the abdomen. It is vital but not essential for life and functions as an indiscriminate filter of the circulating blood. In a healthy individual, the spleen contains about 350ml of blood. The exterior surface of the spleen is surrounded by a layer of peritoneum and inwardly by a connective tissue capsule. The capsule projects inwardly, forming trabeculae that divide spleen into discrete regions. Located within these regions are three types of splenic tissue: a. White pulp - consists of scattered follicles with germinal centers containing lymphocytes, macrophages, and dendritic cells. - Aggregates of lymphocytes surround splenic arteries that pass through these germinal centers. - Adjacent to the splenic arteries is a region called the periarteriolar lymphatic sheath. This area consists of lymphoid nodules containing primarily B lymphocytes. - Activated B lymphocytes are found in the germinal centers. b. Marginal zone - surrounds the white pulp and forms a reticular meshwork containing blood vessels, macrophages, and specialized B cells. c. Red pulp - is composed primarily of vascular sinusoids and sinuses separated by cords of tissue (cords of Billroth) containing specialized macrophages that are loosely connected to the dendritic process, creating a sponge-like region that functions as a filter for blood passing through the region. - As RBCs pass through the cords of Billroth, there is a decrease in flow of blood, which leads to stagnation and depletion of the RBCs glucose supply. - These cells are subject to increased damage and stress that may lead to their removal from the spleen. Note: The spleen uses two methods for removing senescent RBCs from the circulation: a. Culling - in which the cells are phagocytosed with subsequent degradation of cell organelles. b. Pitting - in which splenic macrophages remove inclusions or damaged surface membrane from the circulating RBCs. Functions of the spleen: 1. synthesizes immunoglobulin M in the germinal centers 2. serves as a storage site for platelets.  In a healthy individual, approximately 30% of the total platelet count is sequestered in the spleen. The spleen has a rich blood supply, receiving approximately350 ml/min. Blood enters the spleen through the central splenic artery located at the hilum and branches outward through the trabeculae. The branches enter all three regions of the spleen: the white pulp with its dense accumulation of lymphocytes, the marginal zone, and the red pulp. The venous sinuses, which are located in the red pulp, unite and leave the spleen as splenic veins. Spleen Pathophysiology As blood enters the spleen, it may follow one of two routes. a) Slow-transit pathway - Is through the red pulp in which the RBCs pass circuitously through the macrophages lined cords before reaching the sinuses. - Plasma freely reaches the sinuses, but the RBCs have a more difficult time passing through the tiny openings created by the inter-endothelial junctions of adjacent endothelial cells. Note: The combination of the slow passage and the continued RBC metabolism creates an environment that is acidic, hypoglycemic, and hypoxic. The increased environmental stress on the RBCs circulating through the spleen leads to possible hemolysis. b) Rapid-transit pathway - blood cells enter the splenic artery and pass directly to the sinuses in the red pulp and continue to the venous system to exit the spleen. When splenomegaly occurs, the spleen becomes enlarged and is palpable. This occurs as a result of many conditions, such as chronic leukemias, genetic defects in RBCs, hemoglobinopathies, Hodgkin disease, thalassemia, malaria, and the myeloproliferative disorders. Often splenectomy is beneficial in cases of excessive destruction of RBCs, such as severe hereditary spherocytosis, storage disorders, and autoimmune hemolytic anemias, when treatment with coriicosteroids does not effectively suppress hemolysis. Splenectomy also may be indicated in severe case of agnogenic myeloid metaplasia associated with splenomegaly, severe refractory hemolytic anemia, thrombocytopenia, or qualitative platelet function defect syndromes. After splenectomy, platelet and leukocyte counts increase transiently. In sickle cell anemia, repeated splenic infarcts caused by sickled RBCs trapped into small-vessel circulation of the spleen cause tissue damage and necrosis, which often results in autosplenectomy. Hypersplenism is an enlargement of the spleen resulting in some degree of pancytopenia despite the presence of a hyperactive bone marrow. The most common cause is congestive splenomegaly secondary to cirrhosis of the liver and portal hypertension. Other causes include thrombosis, vascular stenosis, and other vascular deformities such as aneurysm of the splenic artery, and cysts. d. Lymph Nodes Lymph nodes are organs of the lymphatic system located along the lymphatic capillaries that parallel, but are not part of, the circulatory system. The nodes are bean-shaped structures (1 to 5mm in diameter) that occur in groups or chains at various intervals along lymphatic vessels. They may be superficial (inguinal, axillary, cervical, supratrochlear) or deep (mesenteric, retroperitoneal). Lymph is the fluid portion of blood that escapes into the connective tissue and is characterized by a low protein concentration and the absence of RBCs. Afferent lymphatic vessels carry circulating lymph to the lymph nodes. Lymph is filtered by the lymph nodes and exits via the efferent lymphatic vessels located in the hilus of the lymph node. Similar in structure to the spleen, lymph nodes consist of an outer capsule that forms trabeculae and provides support for macrophages and the predominant population of lymphocytes. Lymph nodes can be divided into two basic regions: an outer region called the cortex and an inner region called the medulla. Trabeculae radiate through the cortex and the medulla, dividing the interior of the lymph node into specific areas. In the cortical region, these areas are known as cortical nodules and contain follicles. These follicles contain foci of B-cell proliferation termed germinal centers. The cortical nodules are arranged in circles along the outer cortex region of the lymph node. Located between the cortex and the medulla is a region called the paracortex, which contains predominantly T cells and numerous macrophages. The medullary cords lie toward the interior of the lymph node. These cords consist primarily of B lymphocytes and plasma cells. Lymph nodes have three main functions: (1) they play a role in the formation of new lymphocytes from the germinal centers (2) they are involved in the processing of specific immunoglobulins (3) they filter particulate matter debris, and bacteria entering the lymph node via the lymph. Lymph Node Pathophysiology Lymph nodes, by their nature, are vulnerable to the same organisms that circulate through the tissue. Sometimes increased numbers of microorganisms enter the nodes, overwhelming the macrophages and causing adenitis (infection of the lymph node). More serious is the frequent entry into the lymph nodes of malignant cells that have broken loose from malignant tumors. These malignant cells may establish new growths, which metastasize to other lymph nodes in the same group. e. Thymus To understand the role of the thymus in adults, certain formative intrauterine processes that affect function must be considered: a. the thymus tissue originates from endodermal and mesenchymal tissues. b. the thymus is populated initially by lymphocytes from the yolk sac and the liver. This increased population of lymphoid cells physically pushes the epithelial cells of the thymus apart; however, their long processes remain attached to each other by desmosomes. At birth, the thymus is an efficient, well-developed organ. It consists of two lobules, each measuring 0.5 to 2 cm in diameter. It is located in the upper part of the anterior mediastinum at about the level of the great vessels of the heart. It resembles other lymphoid tissue in that the lobules are subdivided into two areas: the cortex (a peripheral zone) and the medulla (a central zone). Both areas are populated with the same cellular components-lymphocytes, mesenchymal cells, reticular cells, and many macrophages---although in different proportions. The cortex is characterized by a blood supply system that is unique in that it consists only of capillaries. Its function seems to be that of a "waiting zone," which is densely populated with progenitor lymphoid cells that migrated from the bone marrow. These cells have no identifiable surface markers when they enter the thymus but give rise to T cells that later express surface antigens and move toward the medulla. Eventually, they leave the thymus to populate specific regions of other lymphoid tissue such as the T lymphocyte dependent areas of the spleen, lymph nodes, and other lymphoid tissues that are deficient in immunocompetent T lymphocytes. It is theorized that the cytoplasmic processes of the epithelial reticular cells contain secretory products, thymic hormone, thymic factor, and thymic humoral hormones (protein peptides extracted from the thymus) that promote differentiation of pre-T (non-marked) from mature T lymphocytes. The cells that are not marked die in the cortex as a result of apoptosis and are phagocytosed by macrophages before release. The medulla contains only 5% mature T lymphocytes and seem to be a holding zone for conditioned cells until the cells are needed by the peripheral lymphoid tissues. The thymus also contains myriad cell types, including B cells, dendritic cells, eosinophils, neutrophils, and myeloid cells. Cross examination indicates that the size of the thymus is related to age. The thymus weighs 12 to 15 g at birth, increase to 30 to 40 g at puberty, and decreases to 10 to 15 g at later ages. It is hardly recognizable in old age, having atrophies. The thymus retains the ability to produce new T cells, however, as has been shown after irradiation treatment that may accompany bone marrow transplantation. Thymus Pathophysiology Nondevelopment of the thymus during gestation results in the lack of formation of T lymphocytes. Related manifestations seen in patients with this condition are failure to thrive, uncontrollable infections, and death in infancy.  Adults with thymic disturbance are not affected because they have developed and maintained a pool of T lymphocytes for life.