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16.3: Erythrocytes

  • Page ID
    22369
  • By the end of this section, you will be able to:

    • Describe the structure and function of erythrocytes
    • Discuss the various steps in the lifecycle of an erythrocyte

    The erythrocyte, commonly known as a red blood cell (or RBC), is by far the most common formed element. A single drop of blood contains millions of erythrocytes and just thousands of leukocytes. Specifically, males have about 5.4 million erythrocytes per microliter (µL) of blood, and females have approximately 4.8 million per µL. In fact, erythrocytes are estimated to make up about 25 percent of the total cells in the body. Erythrocytes are also smaller than leukocytes and most other body cells, with a mean diameter of only about 7–8 micrometers (µm) (Figure \(\PageIndex{1}\), see Table 16.2.2 Summary of Formed Elements in Blood).

    Due to their chemical properties, oxygen and carbon dioxide molecules largely cannot be transported dissolved in plasma. Thus, the primary functions of erythrocytes are to pick up inhaled oxygen from the lungs and transport it to the body’s tissues, and to pick up some (about 24 percent) carbon dioxide waste at the tissues and transport it to the lungs for exhalation. Although leukocytes typically leave the blood vessels to perform their defensive functions, erythrocytes remain in the blood vessels and movement of erythrocytes from the blood vessels is abnormal.

    Animated View of Formed Elements in a Sample of Blood Viewed Under a Microscope
    Figure \(\PageIndex{1}\): Formed Elements Visible in a Sample of Blood. Erythrocytes are most numerous, significantly smaller than leukocytes, red in color, and biconcave in shape. Leukocytes are the largest and the only formed elements with a discernable nucleus in circulating blood; the shape and position of the nucleus along with the visibility and color of any granules and overall size of the cell distinguish specific leukocytes. Platelets, fragments of a larger cell, are also numerous, but are also the smallest and appear like grains of rice among the other formed elements. (Image credit: "Figure_40_02_01" by OpenStax is licensed under CC BY 4.0)

    Shape and Structure of Erythrocytes

    As an erythrocyte matures in the red bone marrow, it extrudes (pushes out) its nucleus and most of its other organelles. During the first day or two that it is in the circulation, an immature erythrocyte, known as a reticulocyte, will still typically contain remnants of organelles focused on making functional hemoglobin protein complexes. After the first day or two in circulation however, the erythrocyte matures and finishes the differentiation process by shedding its remaining membrane-bound organelles, meaning it will no longer make any new proteins, essentially leaving it as a sac of roughly 300 million hemoglobin molecules. Being absent of organelles also means erythrocytes lack mitochondria, causing them to rely on anaerobic respiration. This means that they do not utilize any of the oxygen they are transporting, maximizing its delivery to the tissues. Reticulocytes do retain some structural proteins, such as the cytoskeletal element spectrin, that help them maintain their unique shape and also enable them to change their shape to squeeze through capillaries. Reticulocytes should comprise approximately 1–2 percent of the erythrocyte count and provide a rough estimate of the rate of erythrocyte production, with abnormally low or high rates indicating problems with underproduction or overproduction of erythrocytes, respectively.

    Erythrocytes are uniquely shaped as biconcave discs; that is, they are plump at their periphery and very thin in the center (Figure \(\PageIndex{2}\)). Since they lack most organelles, there is more interior space for the presence of the hemoglobin molecules that transport gases. The biconcave shape also provides a greater surface area across which gas exchange can occur, relative to its volume; a sphere of a similar diameter would have a lower surface area-to-volume ratio. In the capillaries, the oxygen carried by the erythrocytes can diffuse into the plasma and then through the capillary walls to reach the cells, whereas some of the carbon dioxide produced by the cells as a waste product diffuses into the capillaries to be picked up by the erythrocytes. Capillary beds are extremely narrow, slowing the passage of the erythrocytes and providing an extended opportunity for gas exchange to occur. However, the space within capillaries can be so minute that, despite their own small size, erythrocytes may have to fold in on themselves if they are to make their way through. Fortunately, their structural proteins like spectrin are flexible, allowing them to bend over themselves to a surprising degree, then spring back again when they enter a wider vessel. In wider vessels, erythrocytes may stack up much like a roll of coins, forming a rouleaux, from the French word for “roll.”

    Jn7ws94a-2.jpg
    Figure \(\PageIndex{2}\): Shape of Erythrocytes. Erythrocytes are biconcave discs with very shallow centers. This shape optimizes the ratio of surface area to volume, facilitating gas exchange. It also enables them to fold up as they move through narrow blood vessels. (Image credit: "Jn7ws94a-2" by Annie Cavanagh is licensed under CC BY-SA 4.0)

    Hemoglobin

    Hemoglobin is a large molecule made up of proteins and iron. It consists of four folded chains of a protein called globin, designated alpha chain 1 and 2, and beta chain 1 and 2. Each of these globin molecules is bound to a red pigment molecule called heme, which contains an ion of iron (Fe2+) (Figure \(\PageIndex{3}\)). Each iron ion in the heme can bind to one oxygen molecule; therefore, each hemoglobin molecule can transport four oxygen molecules. An individual erythrocyte may contain about 300 million hemoglobin molecules, and therefore can bind to and transport up to 1.2 billion oxygen molecules.

    1904_Hemoglobin a-only.jpgFigure \(\PageIndex{3}\): Hemoglobin. A molecule of hemoglobin contains four globin protein subunits, each of which is bound to one molecule of the iron-containing red pigmented heme. A single erythrocyte can contain 300 million hemoglobin molecules, and thus more than 1 billion oxygen molecules. (Image credit: "Hemoglobin" by OpenStax is licensed under CC BY 3.0)

    In the lungs, hemoglobin picks up oxygen, which binds to the iron ions, forming oxyhemoglobin. The bright red, oxygenated hemoglobin travels to the body tissues, where it releases some of the oxygen molecules, becoming darker red deoxyhemoglobin, sometimes referred to as reduced hemoglobin. Oxygen release depends on the need for oxygen in the surrounding tissues, so hemoglobin rarely if ever leaves all of its oxygen behind. In the capillaries, carbon dioxide enters the bloodstream. About 76 percent dissolves in the plasma, some of it remaining as dissolved CO2, and the remainder forming bicarbonate ions. About 23–24 percent of it binds to the amino acids in hemoglobin, forming a molecule known as carbaminohemoglobin. From the capillaries, the hemoglobin carries carbon dioxide back to the lungs, where it releases it for exchange of oxygen.

    In determining oxygenation of tissues, the value of greatest interest in healthcare is the percent saturation; that is, the percentage of hemoglobin sites occupied by oxygen in a patient’s blood. Percent saturation is normally monitored using a device known as a pulse oximeter, which is applied to a thin part of the body, typically the tip of the patient’s finger. The device works by sending two different wavelengths of light (one red, the other infrared) through the finger and measuring the light with a photodetector as it exits. Hemoglobin absorbs light differentially depending upon its saturation with oxygen. The machine calibrates the amount of light received by the photodetector against the amount absorbed by the partially oxygenated hemoglobin and presents the data as percent saturation. Normal pulse oximeter readings range from 95–100 percent. Lower percentages reflect hypoxemia, or low blood oxygen. The term hypoxia is more generic and simply refers to low oxygen levels. Oxygen levels are also directly monitored from free oxygen in the plasma typically following an arterial stick. When this method is applied, the amount of oxygen present is expressed in terms of partial pressure of oxygen or simply pO2 and is typically recorded in units of millimeters of mercury, mm Hg.

    The kidneys filter about 180 liters (~380 pints) of blood in an average adult each day, or about 20 percent of the total resting blood volume, and thus serve as ideal sites for receptors that monitor oxygen saturation for the body. In response to hypoxemia, less oxygen will exit the vessels supplying the kidney, resulting in hypoxia (low oxygen concentration) in the tissue fluid of the kidney where oxygen concentration is actually monitored. Interstitial fibroblasts in the connective tissue within the kidney secrete a hormone called erythropoietin (EPO) to stimulate erythrocyte production and restore oxygen levels. In a classic negative-feedback loop, as oxygen saturation rises, EPO secretion falls, and vice versa, thereby maintaining homeostasis. Populations dwelling at high elevations, with inherently lower levels of oxygen in the atmosphere, naturally maintain a hematocrit higher than people living at sea level. Consequently, people traveling to high elevations may experience symptoms of hypoxemia, such as fatigue, headache, and shortness of breath, for a few days after their arrival. In response to the hypoxemia, the kidneys secrete EPO to step up the production of erythrocytes until homeostasis is achieved once again. To avoid the symptoms of hypoxemia, or altitude sickness, mountain climbers typically rest for several days to a week or more at a series of camps situated at increasing elevations to allow EPO levels and, consequently, erythrocyte counts to rise. When climbing the tallest peaks, such as Mt. Everest and K2 in the Himalayas, many mountain climbers rely upon bottled oxygen as they near the summit.

    Lifecycle of Erythrocytes

    Production of erythrocytes in red bone marrow occurs at the staggering rate of more than 2 million cells per second. For this production to occur, a number of raw materials must be present in adequate amounts. These include the same nutrients that are essential to the production and maintenance of any cell, such as glucose, lipids, and amino acids. However, erythrocyte production also requires several trace elements including not only iron, but copper, zinc, and the B vitamins folic acid (folate) and vitamin B12.

    Erythrocytes live up to 120 days in circulation, after which the worn-out cells are removed by a type of myeloid phagocytic cell called a macrophage, located primarily within the red bone marrow, liver, and spleen. Organelles within the macrophages break down the hemoglobin and plasma membrane components of the erythrocytes. The amino acid, heme, and iron components of the degraded erythrocytes’ hemoglobin are recycled when possible. Iron is transported in the blood plasma bound to transferrin and may be transferred to the protein ferritin for storage in the liver. The non-iron portion of heme is degraded into the waste products biliverdin, a green pigment, and then bilirubin, a yellow pigment. Bilirubin binds to albumin and travels in the blood to the liver, which uses it in the synthesis of bile, a compound released into the intestines to help emulsify dietary fats. In the large intestine, bacteria breaks the bilirubin apart from the bile and converts it to urobilinogen and then into stercobilin. It is then eliminated from the body in the feces. Broad-spectrum antibiotics typically eliminate these bacteria, which may alter the color of feces. The kidneys also remove any circulating bilirubin and other related metabolic byproducts such as urobilins and secrete them into the urine.

    The breakdown pigments formed from the destruction of hemoglobin can be seen in a variety of situations. At the site of an injury, biliverdin from damaged erythrocytes produces some of the dramatic colors associated with bruising. With a failing liver (or an underdeveloped one soon after birth), bilirubin cannot be removed effectively from circulation and causes the body to assume a yellowish tinge associated with jaundice. Stercobilins within the feces produce the typical brown color associated with this waste while the yellow of urine is associated with the urobilins.

    The erythrocyte lifecycle is summarized in Figure \(\PageIndex{4}\).

    Flow diagram depicting the life cycle of a red blood cell.
    Figure \(\PageIndex{4}\): Erythrocyte Lifecycle. Hemopoiesis of erythrocytes begins in the hemopoietic bone marrow, where erythroblasts are derived from stem cells and then differentiate into reticulocytes. Reticulocytes are released into the bloodstream, where they mature into erythrocytes, which circulate for an average of 120 days. Old and damaged erythrocytes are phagocytized by macrophages in the bone marrow, liver, and spleen. The globin (protein) portion of hemoglobin is metabolized into amino acids, which are reused for protein synthesis. Lysosomes in the macrophage recycle the other cell components (organelles, membrane structures, etc). The heme portion is broken down into biliverdin for transport in the blood. The iron ions bind to the protein transferrin for transport. Unused heme groups can be recycled and used in hemopoiesis, or can be converted into bilirubin and used to make bile in the liver. Iron ions can also be transferred to the protein ferritin for storage in the liver. (Image credit: "Erythrocyte Life Cycle" by OpenStax is licensed under CC BY 3.0)

    DISORDERS OF THE....

    Erythrocytes

    Changes in the levels of erythrocytes can have significant effects on the body’s ability to effectively deliver oxygen to the tissues. Ineffective hematopoiesis results in insufficient numbers of erythrocytes and results in one of several forms of anemia. An overproduction of erythrocytes produces a condition called polycythemia. The primary drawback with polycythemia is not a failure to directly deliver enough oxygen to the tissues, but rather the increased viscosity of the blood, which makes it more difficult for the heart to circulate the blood.

    The size, shape, and number of erythrocytes, and the number of hemoglobin molecules can have a major impact on a person’s health. When the blood is not carrying sufficient oxygen to the tissues, the general condition is called anemia. There are more than 400 types of anemia and more than 3.5 million Americans suffer from this condition related typically to an insufficient number of erythrocytes or a deficiency of hemoglobin. Anemia can be broken down into three major groups: those caused by blood loss, those caused by faulty or decreased erythrocyte production, and those caused by excessive destruction of erythrocytes. Clinicians often use two groupings in diagnosis: The kinetic approach focuses on evaluating the production, destruction, and removal of erythrocytes, whereas the morphological approach examines the erythrocytes themselves, paying particular emphasis to their size and shape. A common test is the mean corpuscle volume (MCV), which measures size. Normal-sized cells are referred to as normocytic, smaller-than-normal cells are referred to as microcytic, and larger-than-normal cells are referred to as macrocytic. Reticulocyte counts are also important and may reveal inadequate production of erythrocytes. The effects of the various anemias are widespread, because reduced numbers of erythrocytes or hemoglobin will result in lower levels of oxygen being delivered to body tissues. Since oxygen is required for tissue functioning, anemia produces fatigue, lethargy, and an increased risk for infection. An oxygen deficit in the brain impairs the ability to think clearly, and may prompt headaches and irritability. Lack of oxygen leaves the patient short of breath, even as the heart and lungs work harder in response to the deficit.

    Blood loss anemias are fairly straightforward. In addition to bleeding from wounds or other lesions, these forms of anemia may be due to ulcers, hemorrhoids, inflammation of the stomach (gastritis), and some cancers of the gastrointestinal tract. The excessive use of aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen can trigger ulceration and gastritis. Excessive menstruation and loss of blood during childbirth are also potential causes.

    Anemias caused by faulty or decreased erythrocyte production include sickle cell anemia, iron deficiency anemia, vitamin deficiency anemia, and diseases of the red bone marrow and stem cells.

    • A characteristic change in the shape of erythrocytes is seen in sickle cell disease (also referred to as sickle cell anemia). A genetic disorder, it is caused by production of an abnormal type of hemoglobin, called hemoglobin S, which delivers less oxygen to tissues and causes erythrocytes to assume a sickle (or crescent) shape, especially at low oxygen concentrations (Figure \(\PageIndex{5}\)). These abnormally shaped cells can then become lodged in narrow capillaries because they are unable to fold in on themselves to squeeze through, blocking blood flow to tissues and causing a variety of serious problems from painful joints to delayed growth and even blindness and cerebrovascular accidents (strokes). Sickle cell anemia is a genetic condition particularly found in individuals of African descent.
    Normally shaped red blood cells described as biconcave discs in view with a sickled red blood cell shaped like a crescent moon.
    Figure \(\PageIndex{5}\): Sickle Cells. Sickle cell anemia is caused by a mutation in one of the hemoglobin genes. Erythrocytes produce an abnormal type of hemoglobin, which causes the cell to take on a sickle or crescent shape. (Image credit: "Sickle Cells" by OpenStax is licensed under CC BY 3.0)
    • Iron deficiency anemia is the most common type and results when the amount of available iron is insufficient to allow production of sufficient heme. This condition can occur in individuals with a deficiency of iron in the diet and is especially common in teens and children as well as in vegans and vegetarians. Additionally, iron deficiency anemia may be caused by either an inability to absorb and transport iron or slow, chronic bleeding.
    • Vitamin-deficient anemias generally involve insufficient vitamin B12 and folate.
      • Megaloblastic anemia involves a deficiency of vitamin B12 and/or folate, and often involves diets deficient in these essential nutrients. Lack of meat or a viable alternate source, and overcooking or eating insufficient amounts of vegetables may lead to a lack of folate.
      • Pernicious anemia is caused by poor absorption of vitamin B12 and is often seen in patients with Crohn’s disease (a severe intestinal disorder often treated by surgery), surgical removal of the intestines or stomach (common in some weight loss surgeries), intestinal parasites, and AIDS.
      • Pregnancies, some medications, excessive alcohol consumption, and some diseases such as celiac disease are also associated with vitamin deficiencies. It is essential to provide sufficient folic acid during the early stages of pregnancy to reduce the risk of neurological defects, including spina bifida, a failure of the neural tube to close.
    • Assorted disease processes can also interfere with the production and formation of erythrocytes and hemoglobin. If myeloid stem cells are defective or replaced by cancer cells, there will be insufficient quantities of erythrocytes produced.
      • Aplastic anemia is the condition in which there are deficient numbers of the stem cells used to produce erythrocytes. Aplastic anemia is often inherited, or it may be triggered by radiation, medication, chemotherapy, or infection.
      • Thalassemia is an inherited condition typically occurring in individuals from the Middle East, the Mediterranean, African, and Southeast Asia, in which maturation of the erythrocytes does not proceed normally. The most severe form is called Cooley’s anemia.
      • Lead exposure from industrial sources or even dust from paint chips of iron-containing paints or pottery that has not been properly glazed may also lead to destruction of the red marrow.
    • Various disease processes also can lead to anemias. These include chronic kidney diseases often associated with a decreased production of EPO, hypothyroidism, some forms of cancer, lupus, and rheumatoid arthritis.

    In contrast to anemia, an elevated erythrocyte count is called polycythemia and is detected in a patient’s elevated hematocrit. It can occur transiently in a person who is dehydrated; when water intake is inadequate or water losses are excessive, the plasma volume falls. As a result, the hematocrit rises. For reasons mentioned earlier, a mild form of polycythemia is chronic but normal in people living at high altitudes. Some elite athletes train at high elevations specifically to induce this phenomenon. Finally, a type of red bone marrow disease called polycythemia vera (from the Greek vera = “true”) causes an excessive production of immature erythrocytes. Polycythemia vera can dangerously elevate the viscosity of blood, raising blood pressure and making it more difficult for the heart to pump blood throughout the body. It is a relatively rare disease that occurs more often in men than women, and is more likely to be present in patients over 60 years of age.

    Concept Review

    The most abundant formed element in blood, erythrocytes are red, biconcave discs packed with an oxygen-carrying compound called hemoglobin. The hemoglobin molecule contains four globin proteins bound to a pigment molecule called heme, which contains an ion of iron. In the bloodstream, iron picks up oxygen in the lungs and drops it off in the tissues; the amino acids in hemoglobin then transport some carbon dioxide from the tissues back to the lungs. Erythrocytes live only 120 days on average, and thus must be continually replaced. Worn-out erythrocytes are phagocytized by macrophages and their hemoglobin is broken down. The breakdown products are recycled or removed as wastes; globin is broken down into amino acids for synthesis of new proteins; iron is stored in the liver or spleen or used by the bone marrow for production of new erythrocytes; and the remnants of heme are converted into bilirubin, or other waste products that are taken up by the liver and excreted in the bile or removed by the kidneys. Anemia is a deficiency of erythrocytes or hemoglobin, whereas polycythemia is an excess of erythrocytes.

    Review Questions

    Q. Which of the following statements about mature, circulating erythrocytes is true?

    A. They have no nucleus.

    B. They are packed with mitochondria.

    C. They survive for an average of 4 days.

    D. All of the above

    Answer

    Answer: A

    Q. A molecule of hemoglobin ________.

    A. is shaped like a biconcave disk packed almost entirely with iron

    B. contains four glycoprotein units studded with oxygen

    C. consists of four globin proteins, each bound to a molecule of heme

    D. can carry up to 120 molecules of oxygen

    Answer

    Answer: C

    Q. The production of healthy erythrocytes depends upon the availability of ________.

    A. copper

    B. zinc

    C. vitamin B12

    D. copper, zinc, and vitamin B12

    Answer

    Answer: D

    Q. Aging and damaged erythrocytes are removed from the circulation by ________.

    A. myeloblasts

    B. monocytes

    C. macrophages

    D. mast cells

    Answer

    Answer: C

    Q. A patient has been suffering for 2 months with a chronic, watery diarrhea. A blood test is likely to reveal ________.

    A. a hematocrit below 30 percent

    B. hypoxemia

    C. anemia

    D. polycythemia

    Answer

    Answer: D

    Critical Thinking Questions

    Q. A young woman has been experiencing unusually heavy menstrual bleeding for several years. She follows a strict vegan diet (no animal foods). She is at risk for what disorder, and why?

    Answer

    A. She is at risk for anemia, because her unusually heavy menstrual bleeding results in excessive loss of erythrocytes each month. At the same time, her vegan diet means that she does not have dietary sources of heme iron. The non-heme iron she consumes in plant foods is not as well absorbed as heme iron.

    Q. A patient has thalassemia, a genetic disorder characterized by abnormal synthesis of globin proteins and excessive destruction of erythrocytes. This patient is jaundiced and is found to have an excessive level of bilirubin in his blood. Explain the connection.

    Answer

    A. Bilirubin is a breakdown product of the non-iron component of heme, which is cleaved from globin when erythrocytes are degraded. Excessive erythrocyte destruction would deposit excessive bilirubin in the blood. Bilirubin is a yellowish pigment, and high blood levels can manifest as yellowed skin.

    Glossary

    anemia
    deficiency of red blood cells or hemoglobin
    bilirubin
    yellowish bile pigment produced when iron is removed from heme and is further broken down into waste products
    biliverdin
    green bile pigment produced when the non-iron portion of heme is degraded into a waste product; converted to bilirubin in the liver
    carbaminohemoglobin
    compound of carbon dioxide and hemoglobin, and one of the ways in which carbon dioxide is carried in the blood
    deoxyhemoglobin
    molecule of hemoglobin without an oxygen molecule bound to it
    erythrocyte
    (also, red blood cell) mature myeloid blood cell that is composed mostly of hemoglobin and functions primarily in the transportation of oxygen and carbon dioxide
    globin
    heme-containing globular protein that is a constituent of hemoglobin
    heme
    red, iron-containing pigment to which oxygen binds in hemoglobin
    hemoglobin
    oxygen-carrying compound in erythrocytes
    hypoxemia
    below-normal level of oxygen saturation of blood (typically <95 percent)
    macrophage
    phagocytic cell of the myeloid lineage; a matured monocyte
    oxyhemoglobin
    molecule of hemoglobin to which oxygen is bound
    polycythemia
    elevated level of hemoglobin, whether adaptive or pathological
    reticulocyte
    immature erythrocyte that may still contain fragments of organelles
    sickle cell disease
    (also, sickle cell anemia) inherited blood disorder in which hemoglobin molecules are malformed, leading to the breakdown of erythrocytes that take on a characteristic sickle shape
    thalassemia
    inherited blood disorder in which maturation of erythrocytes does not proceed normally, leading to abnormal formation of hemoglobin and the destruction of erythrocytes

    Contributors and Attributions

    OpenStax Anatomy & Physiology (CC BY 4.0). Access for free at https://openstax.org/books/anatomy-and-physiology