Signal Transduction Pathways: Basic Hematology

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Comprehensive practice questions covering blood composition, plasma proteins, cellular elements (RBCs, WBCs, Platelets), hematopoiesis regulators, ABO/Rh blood typing, and the stages of hemostasis.

Last updated 5:35 PM on 6/23/26
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25 Terms

1
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What are the two primary components of blood and their approximate percentages of whole blood volume?

Blood consists of Plasma ( 55%~55\%) and Cellular Elements ( 45%~45\%).

2
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In an average adult, what is the typical volume of blood moving within the circulatory system?

55 or 6L6\,L

3
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What is the weight-based composition of blood plasma?

92%92\% water, 7%7\% proteins (Albumins, Globulins, Fibrinogen, and Regulatory proteins), and 1%1\% other solutes (electrolytes, nutrients, gases, and waste).

4
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What are the normal reference ranges for Erythrocytes (RBCs), Leukocytes (WBCs), and Platelets per cubic mm?

Erythrocytes: 4.26.2 million4.2-6.2 \text{ million}; Leukocytes: 4.511 thousand4.5-11 \text{ thousand}; Platelets: 150400 thousand150-400 \text{ thousand}.

5
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Which plasma protein is primarily responsible for maintaining oncotic pressure and acting as a carrier protein?

Albumin

6
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Describe the synthesis and function of the different types of Globulins.

α\alpha & β\beta-globulins are synthesized in the liver and handle transport (e.g., transferrin); γ\gamma-globulins are produced by plasma cells and function as antibodies for immune defense.

7
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What is the clinical consequence of low albumin levels in the plasma?

Edema, caused by the loss of oncotic pressure.

8
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Define Hemoglobin and its primary function.

A tetrameric protein in RBCs composed of 44 globin chains and 44 heme groups; it transports O2O_2 (binding one molecule per heme) and CO2CO_2.

9
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What are the normal Hematocrit (Hct) values for males and females?

Males:  4050%~40-50\%; Females:  3545%~35-45\%.

10
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According to the 'Rule of Three', how are RBC count, Hemoglobin, and Hematocrit related?

Hemoglobin=RBC×3\text{Hemoglobin} = \text{RBC} \times 3 and Hematocrit=Hemoglobin×3\text{Hematocrit} = \text{Hemoglobin} \times 3.

11
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What is the typical lifespan of an Erythrocyte and why is its shape significant?

The lifespan is  120days~120\,\text{days}; its biconcave shape increases surface area for efficient gas exchange and allows flexibility through capillaries.

12
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What is the function and clinical relevance of Neutrophils (PMNs)?

They are early responders that phagocytize bacteria; they represent 5070%50-70\% of WBCs and increase in number during bacterial infections.

13
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Which white blood cell types are expected to increase during viral infections?

Lymphocytes (2040%20-40\% of WBCs).

14
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What clinical condition is associated with an increase in Eosinophils (14%1-4\% of WBCs)?

Parasitic infections and allergies.

15
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Which immature leukocyte is not normally seen in blood but is associated with acute myelogenous leukemia and Auer rods?

Myeloblasts

16
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Where does hematopoiesis occur in adults?

In the red bone marrow, mostly located in the axial skeleton.

17
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What hormone stimulates RBC production, where is it produced, and what triggers its release?

Erythropoietin (EPO); it is produced by the kidneys in response to tissue hypoxia.

18
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Which growth factor promotes platelet formation and where is its source?

Thrombopoietin (TPO), produced by the liver and kidney.

19
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Explain the inheritance and antibody presence in the ABO blood group system.

A and B alleles are codominant, while O is recessive. Individuals possess antibodies against the antigens they lack (e.g., Type O has anti-A and anti-B antibodies).

20
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Under what specific conditions does Hemolytic Disease of the Fetus and Newborn (HDFN) occur?

When an RhRh^- mother is pregnant with an Rh+Rh^+ fetus, leading to the formation of maternal anti-D IgG that can cross the placenta in future Rh+Rh^+ pregnancies.

21
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What are the four major steps of Hemostasis?

  1. Vascular spasm, 2. Platelet plug formation (aggregation), 3. Coagulation (clotting cascade), 4. Fibrinolysis (breakdown of the clot).
22
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During primary hemostasis, how do platelets adhere to exposed collagen?

Via von Willebrand factor and glycoprotein Ib/IX/VIb/IX/V.

23
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At which factor do the intrinsic and extrinsic coagulation pathways converge to begin the common pathway?

Factor XX

24
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Which clotting factors are Vitamin-K dependent?

Factors IIII, VIIVII, IXIX, and XX.

25
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Describe the process of Fibrinolysis.

Plasminogen is converted to Plasmin via tPAtPA; Plasmin then degrades the fibrin mesh to dissolve the clot.