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88 Cards in this Set
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Production of Blood Cells Cellular Formation, Proliferation, Differentiation and Maturation of Blood Cells |
Hematopoiesis |
Yolk Sac=> Liver=> Spleen=> Thymus=> Lymph Node=> BM |
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As early as 19th day gestation in the blood islands of the yolk sac of the human embryo blood pxn starts |
Mesoblastic Stage |
Blood Islands remain active for 8-12 Weeks Hematopoietic activity confined to erythropoiesis |
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First Blood Cell produced by developing embryo |
Erythrocytes/RBCs |
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Embryonic Hemoglobins: |
1. GOWER 1 -2 Zeta, 2 Epsilon
2. GOWER 2 -2 Alpha, 2Epsilon
3. PORTLAND -2 Zeta, 2 Gamma |
ZAZ EEG |
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3rd month Yolk Sac discontinues its role, Fetal Liver becomes active Also active Spleen, thymus, lymph nodes Erythrocytes & Granulocytes in pxn |
Hepatic Stage |
End of 4th month primitive cells disappearing, Inc in more definitive erythroblasts, granulo, & megakaryo |
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Between 5th and 6th month gestation the BM become the primary site of hematopoiesis At Birth, BM primary source of cell pxn |
Myeloid Stage |
Sternum (Flat Bones) - BM Primary Site for Hematopoiesis
Iliac Crest - Safest most accessible site for BM Biopsy |
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Normal Myeloid to Erythroid Ratio (M:E) |
2:1 - 4:1 |
Inc in: 1. Infection (6:1) 2. Leukemia |
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Normocellular Marrow for Adult: |
Fat/Yellow Marrow: 10 - 50% Hematopoietic Elements/Red Marrow: 40-60% Av: 50%
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Child Under 2 yrs has 100% Red Marrow
Retrogression -Replacement of active BM by adipose cells |
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Marrow Differential Recommended Count _______ Preffered Count ________ |
500 1000 |
Predominant Cell in the adult BM: Metamyelocytes/Juvenile |
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Marker for Lymphoid, Pan T Cells |
CD2, CD3 |
CD4 - Helper/Inducer T Cells CD8 - Suppressor/Cytotoxic T Cells |
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Marker for Pan Myeloid |
CD13 |
CD33 -Pan Myeloid Cells |
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Marker for Monocytes |
CD11c, CD14 |
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Marker for Lymphoid, Pan B Cells |
CD19 CD20 |
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Stem Cell Marker (Lymphoid & Myeloid Precursor) |
CD34 |
Stem Cells <1% of cells in BM |
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Marker for NK Cells |
CD16, CD56 |
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Common ALL Antigen |
CD10 |
CALLA |
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Primary regulator of Erythropoiesis |
Erythropoietin (EPO) |
Pronormoblasts to Retics: 3-5 Days
Retics remian in the BM for: 1-2 Days before being released to the circulation
In Peripheral Circulation Retics continue to Mature for: 1 Day |
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Erythropoiesis: |
1. Pronormoblast/ Rubriblast 2. Basophilic Normoblast/ Prorubricyte 3. Polychromatophilic Normoblast/ Rubricyte 4. Orthochromatophilic Normoblast/ Metarubricyte 5. Polychromatophilic Erythrocyte/ Reticulocyte 6. Mature Erythrocyte |
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Deeply Basophilic Cytoplasm Perinuclear Halo lighter area around nucleus N/C Ratio: 8:1 Fine Chromatin |
Pronormoblast/ Rubriblast |
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Intensely Basophilic Cytoplasm Chromatin Pattern Slighlty Coarser N/C Ratio: 6:1 |
Basophilic Normoblast/ Prorubricyte |
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Last stage capable of Cell Division
Start of Hgb Pxn (Blue-gray/Pink-gray cytoplasm)
More condensed; chromatin pattern is coarse & clumped Distinct Parachromatin N/C Ratio: 4:1 |
Polychromatophilic Normoblast/ Rubricyte |
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Last nucleated stage
Pyknotic Nucleus, Partially extruded from the cell
Pinker Cytoplasm (Inc Hgb Pxn) N/C Ratio: 1:2
NUCLEUS EJECTED |
Orthochromatophilic Normoblast/ Metarubricyte |
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Pink to slight pinkish gray Contains a fine basophilic reticulum of RNA Diffusely Basophilic |
Polychromatophilic Erythrocyte/Reticulocyte |
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Pink Color Non-nucleated, round, biconcave cell |
Mature Erythrocyte |
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How many erythrocytes are produced from each pronormoblast |
16 Erythrocytes |
Life Span: 120 Days +/- 20 Days |
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Granulocytic Series: |
1. Myeloblast 2. Promyelocyte 3. Myelocyte 4. Metamyelocyte 5. Band 6. Mature Granulocyte -Segmented Neutro -Eos -Baso |
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Cytoplasm Moderate Blue in Color Smooth, Non-granular Extremely Fine Chromatin N/C Ratio: 4:1 |
Myeloblast |
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Pale Blue to Basophilic Cytoplasm Appearance of Primary/Non-specific Granules N/C Ratio: 2:1 |
Promyelocyte |
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Last stage capable of cell division Appearance of Secondary/Specific Granules N/C Rtaio: 1:1 |
Myelocyte |
Neutro Myelocyte: PINK SPECIFIC GRANULES
Eosinophil Metamyelocyte: ORANGE SPECIFIC GRANULES
Basophil Myelocyte: DARK BLUE-PURPLE GRANULES |
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Indented/Kidney-shaped Nucleus
Chromatin is coarse and clumped and stains dark purple
Full Complement of Specific Granules
Not anymore Capable of Mitosis Predominant Cell in Adult BM |
Metamyelocyte (Juvenile) |
Neutrophil Metamyelocyte: PINKER & more numerous granules
Eosinophil Metamyelocyte: BRIGHTER ORANGE
Basophil Metamyelocyte: DARK PURPLE TO BLACK |
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Youngest stage to normally appear in peripheral blood Elongated/Sausage/Curved Nucleus |
BAND |
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Pink to rose-violet specific granules 2-5 Lobes Coarse, clumped chromatin pattern |
Segmented Neutrophil |
Ferrata Cell |
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Large, reddish orange granules
Usually has 2 Lobes
Coarse, clumped chromatin Pattern |
Eosinophil |
Inc in the Afternoon Primary Suppression of Immune Response |
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Dark purple to blue-black granules
Water Soluble Granules
Unsegmented or Bilobed, rarely has 3-4 lobes |
Basophil |
Rare: 0-1% Effector Cell of Type 1 Hypersensitivity |
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Monopoiesis: |
1. Monoblast 2. Promonocyte (Resemble Neutrophil Band) 3. Monocyte |
Monocyte - Largest cell in Peripheral Bld - Abundant blue-gray cytoplasm, Many Fine azurophilic granules, ground glass appearance - Round, kidney, Horse-shoe shaped - Brain-like convolutions - Skein-like strands of Chromatin - Differentiate to become macrophages |
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Lymphopoiesis: |
1. Lymphoblast 2. Prolymphocyte 3. Mature Lymphocyte -Small Lymphocyte -Medium Lymphocyte -Large Lymphocyte |
Small Lymphocyte - Thin rim around nucleus - Moderate - Dark Blue Cytoplasm
Medium Lymphocyte - More abundant cytoplasm - Pale to moderately blue
Large Lymphocyte - Abundant cytoplasm - Clear, very pale blue |
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Derived from BM Differentiates into plasma cells secretes Igs Humoral Immunity |
B Lymphocytes |
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Mature in Thymus Interact w/ antigens to form specific effector cells Cellular Immunity |
T Lymphocytes |
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Morphologically resemble Large Granular Lymphocytes (LGL) Destruction of Tumor and virus infected cells without Ag specificity or prior sensitization |
Null Lymphocytes/ NK Cells |
Lack characteristic of Mature T & B lymphocytes |
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NK Cells exposed to IL2 which acts against cancer |
Lymphokine-Activated Killer (LAK) Cells |
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Cells mistaken as Lymphocytes: |
1. Monocytes 2. Blasts 3. Rubricytes |
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Plasma Cells: |
1. Plasmablast 2. Proplasmacyte 3. Plasmacyte/Plasma Cell |
Plasmablast - Basophilic Cytoplasm - Red/Pink Cyst, Flame
Proplasmacyte - Intensely Basophilic - HOF/Perinuclear Halo
Plasmacyte/Plasma Cell - Deeply Basophilic - Cart-wheel-like pattern Nucleus |
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Each megakaryocyte generally produces _____________ Platelets |
2,000 - 4,000 Platelets |
Megakaryocyte - Cell w/c gives rise to blood platelets |
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It takes how many days for megakaryocyte to mature in the BM |
4-5 Days |
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Hormone produced by the liver & kidney which influences maturation of platelets |
Thrombopoietin (TPO) |
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Megakaryopoiesis/ Thrombopoiesis |
1. Megakaryoblast 2. Promegakaryocyte 3. Granular Megakaryocyte 4. Mature Megakaryocyte (Metamegakaryocyte) 5. Platelet (Thrombocyte) |
Megakaryoblast - Where endomitosis Starts Promegakaryocyte - Where Endomitosis (nuclear division w/out cytodivision) ends |
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Invagination of the plasma membrane that becomes the future site of platelet fragmentation |
Demarcating System (DMS) |
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Platelets life span once released to the peripheral blood |
9-12 Days |
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2/3 of Plts are in the 1/3 of Plts are in the |
BLOOD SPLEEN |
Platelet Factors: PF3 - Platelet phospholipid needed for proper platelet function PF4 - Neutralizes Heparin |
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Contains coarse clumps of granules aggregating into little bundles, bud off from the periphery to become platelets Multiple Nuclei |
Mature Megakaryocyte/Metamegakaryocytes |
40-120 um |
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Programmed Cell Death Cell Shrinkage Condensation of Nucleus |
Apoptosis |
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Cell Swelling Karyolysis Pathologic |
Necrosis |
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Light Blue to purple cytoplasm Very Granular |
Platelet/ Thrombocyte |
Consists of 2 Parts: Chromomere - Granular, located centrally
Hyalomere - Surrounds the chromomere and is non-granular and clear to light blue |
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Start of Endomitosis: |
LD-Meg (New Rodak) MK-1 (Old Rodak) |
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Four Areas of Platelet Structure: |
1. Peripheral Zone 2. Sol-gel Zone 3. Organelle Zone 4. Membranous System |
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Responsible for Platelet Adhesion and Aggregation |
Peripheral Zone |
Adhesion - Plt to Blood vessel surface Aggregation - Platelet to Platelet Consists of: 1. Glycocalyx 2. Plasma Membrane 3. Sub-membranous Area |
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External Surface of the platelet
Composed of glycoproteins including coag factors 5, 8 & Fibrinogen |
Glycocalyx |
Important in plt reactions w/ thrombin, vWF, & Fibrinogen |
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Lies beneath glycocalyx Composed of a bilayer of asymmetrically distributed phospholipids embedded w/ integral proteins, arachidonic acid is a major component |
Plasma Membrane |
GpIb - receptor for vWF GP IIb & IIIa - Receptors for fibrinogen |
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Provide a cytoskeleton to maintain platelet shape, a contractile system |
Sol-Gel Zone |
Consists of: 1. Microfilaments 2. Microtubules |
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Contain the proteins actin & myosin Upon stimulation of platelet, will interact to form Actomyosin (Thrombosthenin) |
Microfilaments |
Actomyosin (Thrombosthenin) - A contractile protein, important in clot retraction |
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Composed of protein tubulin, which maintains the platelet's disc shape |
Microtubules |
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Responsible for platelet aggregation and Generation of ATP |
Organelle Zone |
Consists of: 1. Alpha Granules 2. Dense Bodies 3. Mitochondria 4. Lysosomal Granules |
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Important for ATP Synthesis for platelet metabolism |
Mitochondria |
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Contain ACP & Hydrolytic Enzymes |
Lysosomal Granules |
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Membranous System: |
1. Dense Tubular System 2. Surface Connecting System (Open Canlicular System) |
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Derived from the smooth reticulum and sequesters (holds) calcium for platelet activation processes
Also synthesizes prostaglandins |
Dense Tubular System |
Control System Site of Arachidonic Acid Metabolism to form TXA2 |
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Invagination of the plasma membrane, acts as canal for the release of the granule constituents and cytoplasm to the exterior of the platelet |
Surface Connecting System (Open Canalicular System) |
Also involved in Platelet Phagocytosis |
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The hemoglobin molecule is composed of four subunits, each containing |
Heme (4) Globin (4) |
*1 Heme Carries 1 Mole of Oxygen |
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Synthesis of Heme begins in the |
Mitochondria |
With the formation of D-ALA from Glycine & Succinyl Coenzyme A |
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Chromosome 16 codes for |
Alpha Zeta |
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Chromosome 11 codes for |
1. Gamma 2. Beta 3. Epsilon 4. Delta |
GBED |
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Newborn & Adult Hemoglobins |
1. HbA1 2 Alpha, 2 Beta 2. HbA2 2 Alpha, 2 Delta 3. HbF (Fetal) 2 Alpha, 2 Gamma |
ABADAG |
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Influence of pH on the release of oxygen from Hgb |
Bohr Effect |
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Oxyhemoglobin Dissociation Curve |
Sigmoidal |
Indicates Low Hgb Affinity for oxygen @ low oxygen tension & high affinity for oxygen at high oxygen tension |
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Shift to the Right |
Inc Blood Temp, 2,3 DPG, CO2 Dec pH |
Decreased Affinity for O2 |
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Shift to the Left |
Inc pH, HbF admixture Dec Blood Temp, 2,3 DPG, CO2 |
Increased Affinity for O2 |
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Gives Blood a Cherry Red Color Light Sensitive Increase Conc shifts the Hgb-O2 Dissociation Curve to the LEFT Cannot bind & Carry Oxygen Hgb bound to Carbon Monoxide |
Carboxyhemoglobin |
Pink CSF Quantitated by: 1. Differential Spectrophotometry 2. Gas Chromatography |
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Oxygen derivative in which the Ferrous iron is not oxidized to Ferric state resulting to inability to combine reversibly w/ oxygen
Gives Blood a Chocolate Brown discoloration |
Methemobglobin/Hemiglobin (Hi) |
Other Causes: 1. Methgb Reductase Def 2. Chem/Drugs (Chlorate, Nitrate, Nitrite) 3. Hgb M
*Quantitated using Spectrophotometry |
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An abnormal Hgb that may also be responsible for Methgbinemia noted at birth or in the first few months of life Px is Cyanotic |
Hgb M |
Treated w/ Methylene Blue |
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Mixture of oxidized, partially denatured forms of Hgb that form during oxidative lysis
Blood is Mauve-Lavander color Irreversible |
Sulfhemoglobin |
Quantitated by Spectro |
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Reported in Pxs: 1. Treatment w/ sulfonamides or aromatic amine drugs (Phenacitin, Acetanilid) 2. Severe Constipation 3. C. perfringens Infection 4. Enterogenous Cyanosis |
Sulfhemoglobin |
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Maintains the iron in its ferrous state for it to be functional |
Methgb Reductase |
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Cyanmethgb Method can measure all forms of oxygen exc: |
Sulfhemoglobin |
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Adult Hgb Normal Distribution |
HbA1 >/= 95% HbA2 1.5-3% HbF <1-2% |
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Neonatal Hgb Normal Distribution |
HbF 60-80% HbA 20-40% |
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Multi-CSF Multi-Lineage Colony Stimulating Factor Stimulates Hematopoietic Cells |
IL-3 |
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Most potent phagocytic Cell
Most efficient APC
From: Common Lymphoid Progenitor |
Dendritic Cells |
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Not an End Cell |
Monocytes B Cells |
Rodak: B Cells |