TBL14 - Bone Marrow Flashcards Preview

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Flashcards in TBL14 - Bone Marrow Deck (18):
1

Endothelial cells and blood cells are derivatives of what type of cell? What do these cells initially form in the embryo? What does this develop into and when?

1) Endothelial cells and blood cells are derivatives of hemangioblasts
2) Hemangioblast-derived hematopoietic stem cells initially form blood islands in mesoderm surrounding the yolk sac
3) The stem cells subsequently colonize the liver, which is the major hematopoietic organ from the 2nd to 7th month of gestation

2

What occurs in the 7th month of the embryo/fetus?

In the 7th month, stem cells from the liver colonize the bone marrow that becomes the definitive blood-forming tissue after birth

3

Compare the two microscopic methods for studying bone marrow. Define common sites for aspirations and needle biopsies of the bone marrow and compare their clinical applications.

1) Smears and trephine needle biopsy (for preparation of bone marrow sections) are used to sample and examine bone marrow
2) The optimal site for both aspiration and trephine biopsies is the posterior iliac crest, other sites being the sternum and tibia
3) Smears are the best preparations for evaluating cell details, studying maturation of hematopoietic cells, making differential counts, and assessing the ratio of myeloid (leukocyte) to erythroid (erythrocyte) cells. An advantage is preservation of individual cells so that subtle morphologic changes and infiltration by malignant cells in disease can be detected. Smears can also detect anemias, leukemias, and myeloma
4) The trephine biopsy entails cutting out a solid core of bone marrow, including some trabecular bone, with a large-bore cutting needle. Sections are less valuable than smears for elucidating cell details but provide a panoramic view of bone marrow and its normal architecture. They are also useful for estimating bone marrow cellularity, which is an index of the proportion of hematopoietic cells to adipocytes. Bone marrow cellularity is high in young persons, is reduced in the elderly, and may be altered in disease

4

How do autologous and allogeneic bone marrow transplants differ?

1) Autologous transplantation is used in certain forms of lymphoma in which malignant cells contaminate marrow. It involves harvesting bone marrow stem cells from a patient, followed by highdose chemotherapy and then intravenous injection of reconstituted marrow
2) A stem cell transplant from another person is an allogeneic transplant. Its success requires donor matching for the major histocompatibility complex (MHC) on chromosome 6

5

Are blood cells long- or short-lived? What is a result of this?

Most blood cells are short-lived; thus, continuous blood cell replacement is provided by hemangioblast-derived pluripotential hematopoietic stem cells that reside in the bone marrow and have the capacity for self-renewal, replication, and differentiation

6

What is the difference between a progenitor cell and a colony-forming unit (CFU)?

1) Progenitor cells are direct descendants of the pluripotential stem cells
2) When injected experimentally into the spleen, progenitor cells proliferate into colony-forming units (CFUs); thus progenitor cells and CFUs are interchangeable terms

7

Name the CFUs. What do CFUs differentiate into?

1) CFUs committed to erythroid lineage production contain progenitor cells known as colony-forming unit-erythrocytes (CFU-E)
2) Granulocyte and monocyte cell lines develop from one progenitor cell known as the colony-forming unit-granulocyte-monocyte (CFU-GM). As cells mature, progeny become committed to either granulocytes or monocytes
3) Cells of the lymphocyte lineage are generated from colony-forming unit-lymphocytes (CFU-L)
4) Progenitor cells for megakaryocytes produce colonies that contain colony-forming unit-megakaryocytes (CFU-Me)
5) CFUs differentiate into precursor cells that can be recognized microscopically as members of specific blood cell lineages i.e., like the CFUs, there are erythrocytic, granulocytic, monocytic, lymphocytic, and thrombocytic precursor cells

8

What are RBCs derived from? What are PMNs, eosinophils, basophils, and monocytes derived from? What are lymphocytes derived from? What are platelets derived from?

1) RBCs are derived from CFU-E via erythropoiesis
2) PMNs, eosinophils, basophils, and monocytes are derived from CFU-GM via granulopoiesis and monocytopoiesis
3) Lymphocytes are derived from CFU-L via lymphocytopoiesis
4) Platelets are derived from megakaryocytes

9

What are the first precursor cells derived from CFU-E? What characterizes the lineage of erythroblasts? Distinguish the basophilic, polychromatophilic, and orthochromatophilic erythroblasts.

1) During erythropoiesis, proerythroblasts are the first precursor cells derived from CFU-E
2) During the differentiation of erythrocytes, progressive cytoplasmic color changes characterize the lineage of erythroblasts
3) BE have a large dark purple central mass; PE has a smaller dark purple central mass with a slightly lighter shade of purple surrounding it; No has a very dark purple mass with an extremely light pink shade surrounding it

10

What occurs to the nucleus during erythropoiesis? What is different between reticulocytes and erythrocytes?

1) The progressive nuclear condensation during erythropoiesis
2) Nuclear extrusion occurs in the later stages
3) Reticulocytes are anucleate but unlike erythrocytes, lack central pallor

11

What does erythropoietin do? Define the normal duration of erythropoiesis.

1) Erythropoietin, which is produced in the kidneys, stimulates and sustains erythropoiesis
2) Erythropoiesis, from the proerythroblast to the mature erythrocyte, takes 7-8 days

12

Why is hypoxia the principal stimulus for erythropoietin secretion?

1) Erythropoiesis is regulated by the glycoprotein hormone erythropoietin, which is secreted by interstitial peritubular cells of the kidneys, mostly in response to hypoxia
2) This is due to the fact that bodily tissues are not receiving enough oxygen and require more erythrocytes to bind and transport oxygen to the body

13

Why does cytoplasmic color change from blue to reddish pink during erythropoiesis?

1) The CFU-erythrocyte first differentiates into the earliest recognizable cell of this series: a large, round proerythroblast, with a diameter of 15-30 mm. Its deep blue cytoplasm is due to abundant ribosomal RNA, which has affinity for basic dyes
2) Central pallor causes pink color (lack of nucleus/rRNA)

14

What are the first precursor cells derived from CFU-GM? What is noticeable about them microscopically?

1) During granulopoiesis, the first precursor cells derived from CFU-GM are myeloblasts that appear similar to the proerythroblasts microscopically
2) Thus, you are not expected to distinguish myeloblasts and proerythroblasts in the bone marrow smears

15

What do myeloblasts differentiate into? What occurs during the transformation of promyelocytes into myelocytes?

1) Myeloblasts differentiate into promyelocytes with large, round nuclei and reddish blue cytoplasmic granules (lysosomes)
2) During transformation of promyelocytes into myelocytes, the nuclei become eccentrically positioned and flattened on one side

16

What occurs during the transformation of myelocytes into metamyelocytes? What occurs during differentiation of metamyelocytes?

1) Indentation of the flattened side of the myelocytic nuclei occurs during transformation of myelocytes into metamyelocytes
2) Neutrophilic, eosinophilic, and basophilic granules in the cytoplasm become more distinct during differentiation of the metamyelocytes

17

What transforms the metamyelocytes into band cells with horseshoe-shaped nuclei? What completes the maturation process of these cells? Cite the normal duration of granulopoiesis.

1) Progressive deepening of the metamyelocytic nuclear indentations transforms the metamyelocytes into band cells with horseshoe-shaped nuclei
2) Lobulation of the horseshoe-shaped nuclei completes the maturation process
3) The maturation sequence whereby the three types of granulocytes are produce —granulocytopoiesis— takes 14-18 days

18

What is sepsis and when can it progress to septic shock?

1) Sepsis is a potentially life-threatening systemic response to infection (Blood poisoning is the nonscientific lay term for it)
2) The pathogenesis includes the presence in bloodstream of an infectious agent (e.g., bacteria, fungi, parasites)
with release of endotoxins
3) Signs of inflammation (e.g., vasodilation, leukocyte accumulation, increased microvascular permeability) typically occur in tissues remote from cause of infection
4) Symptoms include an abnormal body temperature (>38°C or 12,000/mL or < 4,000/mL or >10% band cells)
5) Patients may progress to more serious septic shock when hypotension and organ dysfunction fail to respond to antimicrobial treatment

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