Thrombocytes are formed in the bone marrow
Platelets can contract via myosin and actin
Thrombocytes store Ca++
Platelets reproduce in the golgi apparatus of Megakaryocytes
Platelets have a half life of 8-12 days
Platelets are not capable of activating eachother
Plug formation is efficient for all sizes of openings in vessel walls/ structures
Platelets don't play a role in cloth retraction
Blood cloths become invaded by fibroblasts which further form connective tissue
Calcium is facto V
Factor XIII is fibrin stabilising factor
Factor I is Fibrinogen
Prothrombin receptors are present on platelets
Prothrombin is formed in the Liver
Vitamin K deficiency results in a bleeding tendency
Fibrinogen is formed in the bone marrow
Serum can not clot
Clot retraction is carried out by Platelets, Ca++ and Thrombin
A wettable surface like glass can convert factor XII to XIIa
Fibrinogen is formed in the bone marrow
Tissue factor release - Factor X activation - Thrombin - prothrombin
Prothrombin - Thrombin - Factor X activation - Tissue factor release
Tissue factor release - Factor X activation - Prothrombin - Thrombin
Factor X activation - Prothrombin - Thrombin - Tissue factor release
Heparin is highly positively charged
Alone, it is useless as an anticoagulant
Factors XII, XI, X, and IX are removed by heparin and antithrombin III
Heparin in high amounts inhibits clot formation
Haemophilia A is caused by a deficiency of Factor VIII
Splenectomy is always a cure for thrombocytopenia
Factor VIII can be injected into a haemophilia A patient to effectively cure for a short while
Minute Haemorrhages are apparent throughout the body in Thrombocytopenia
The bone marrow
The spleen
The liver
The pancreas
It has a vast number of macrophages lodged in its trabeculated region and venous sinusoids.
It is responsible for defending the body against blood born organisims
It is a hypoxic and alkaline environment
It is involved in haemolytic anaemias
Major basic protein
Hypochlorite
Lysozyme
Perforins
IL-2
IL-1
IL-6
IL-5
IL-3
IL-4
IL-5
IL-6
C3bBb
C3(H20)Bb
C3bBbC3b
C4bC2b
C5a is a chemotactic agent
C5a and C3a are activators of phagocytosis
C4b has anti-viral properties
C4a can act as an opsinizing agent
Cleaving fluid phase C3 convertase
Binding to free C3b
Binding to free Factor D
Causing the dissociation of C1 from the gamma CH2
Bradykinin
Histamine
Eosinophile chemotactic factor
Il-4
Activation induced Kinase
Thymine-DNA Glycosylase
Error Prone DNA Polymerase
DNA-Uracil Glycosylase
IgM can become any other class
IgG type 3 can become IgG type 1
IgA1 can become IgA2
Switch sites are present before the gene coding for every class except for the Delta gene
Tissue Macrophage activation-Macrophge invasion-Neutrophile invasion-Bone marrow activation
Tissue Macrophage activation-Bone Marrow activation-Neutrophile Invasion-Macrophage invasion
Neutrophile Invasion- Macrophage Invasion-Bone Marrow activation-Tissue Macrophage activation
Tissue Macrophage activation-Neutrophile invasion-Macrophage invasion-Bone Marrow activation
IL-1
TNF
G-CSF
IL-2
Both neutrophils and macrophages can phagocytose and destroy all types of bacteria
Both are capable of excreting the products of phagocytosis by exocytosis
Both Make use of peroxisomes to aid in the digestion process
Both make use of the enzyme myeloperoxidase to form OH-. radicals
Suffocation due to histamine
Suffocation due to the slow reacting substance of anaphylaxis
Circulatory shock due to histamine
Circulatory shock due to the slow reacting substance of anaphylaxis
T-Helper cells
IgEs and Basophils
Cytotoxic T-cells
Neutrophils
5 degrees celcius
15 degrees celcius
22 degrees celcius
-30 degrees celcius
The red blood cell storage leision can be due to white blood cells present in the blood
The red blood cells in stored blood may develop an abnormaly low affinity for oxygen
The red blood cells may be damaged by ROS while in storage
The blood transfused will be more acidic than when collected.
Involved in biding to alpha CH2 regions on the heavy chains of antibodies
Composed of 2 C1r and C1s subunits as well as a C1p subunit
A zymogen that when activated catalyses the amplification loop
A complement protein involved in only the classical pathway
Members of the granulocyte family
Responsible for releasing ROS
The first cells to respond in an inflammatory response
Able to enter a tissue by diapedisis
Basophils
Cytotoxic T-cell
Eosinophils
Macrophages
Acute myelogenous leukemia
Chronic myelogenous leukemia
Acute Lymphoblastic leukemia
Chronic Lymphocytic leukemia
An attack on synovial joints
An attack on Ne Receptors on skeletal muscles
An attack on AcH receptors on skeletal muscles
An attack of the basement membrane of the glomerulus
5 days
5 hours
12 hours
7 days
Alpha defensin
IgA
Resident Macrophages
T and B lymphocytes
The female reproductive system varies in its susceptibility to disease
The male reproductive system shares the urinary systems defences
The Skin is highly resistant to microbes by virtue of having an acidic pH
The interleukin IL-2 is part of the urinary defence system
T-cells contribute to immunity
Immunization is passive artificial immunity
Anti-serum lasts a couple of months
Anti-serum is passive immunity
Granulocytes last 4-8 days in blood
Lymphocytes last weeks or months
Monocytes mature in blood
Monocytes last months after entering tissues
The neutrophil projects Psuedopodia in one direction, which wraps around the foreign cell
A neutrophil can only ingest one bacterium before inactivating
Neutrophil Phagocytosis begins with fusion of pseudopodia with foreign particle
Fusion of pseudopodia occurs at the other end of an invaginated particle forming a phagosome
O2
H2O2
OH-
O2-
Histocytes
Lymph nodes
Kuppfer cells
Vascular endothelial cells
In the thymus, immature basophils undergo rapid division and differentiation
Self antigen presenting lymphocytes in the thymus are destroyed by a process known as Clonal Selection
Pre-Processing of B lymphocytes occurs in the Liver throughout life
Lymphocyte pre-processing occurs only shortly before birth, and slightly after
IL-3
IL-6
IL-1
IL-4
Memory cells are the basis of vaccination
Plasmablasts are precursors of erythrocytes
Memory cells are produced in high numbers irrespective of infection
Plasma cells undergo rapid division forming immature Plasma cells
Activated C1 is involved in the formation of C4b, C2a, C4a and C2b
C4Bp is capable of inhibiting C4b
C5 convertase is composed of C2b, C3b, C4b and C4a
C3bC4b complex promotes phagocytosis
Factor H inhibits only free C3b
Factor I cleaves C3b
The complement pathway is tightly regulated
MBLs and Ficolins are associated with MASPs
Metabolic starvation results due to the bodys extra needs to combat cancer
It is a result of Metastatic growth of Erythrocytic Tissues
There is a tendency for bleeding
Individuals die of irriversible cell damage
Type 1 diabetes
Myasthenia gravis
Glomerulonephrritis
Acute Porphyria
DAF
ACR
CR1
MCP
Plasmaphoresis
Erythrocytapheresis
Thrombopheresis
Leukapheresis
Platelets last 10 days at 4 Degrees temperature
Plasma lasts for 2 years at room temperature
Erythrocytes last for 42 days at 4 degrees celcius
Cryoprecipitate lasts for 2 years at 4 degrees
Dextrose
NaHPO4
Adenine
Citrate
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