BSCI202 Exam 1 Study Guide: Blood, Lymph, and Immune System

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Vocabulary flashcards covering blood components, hemostasis, immune defenses, blood typing, and the lymphatic system.

Last updated 5:15 PM on 9/20/26
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38 Terms

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Hematocrit

The percentage of total blood volume composed of erythrocytes (RBCs), which averages approximately 45%45\% in a healthy individual.

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Albumin

The main plasma protein responsible for maintaining osmotic balance and buffering pH in the blood.

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Serum

The liquid portion of blood that remains after clotting factors have been consumed by clot formation.

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Hemocytoblast (Hematopoietic Stem Cell)

The progenitor stem cell located in red bone marrow from which all formed elements of the blood originate.

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Oxyhemoglobin

Hemoglobin bound to oxygen (O2O_2) immediately after loading in the lungs, giving blood a ruby red color.

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Carbaminohemoglobin

Hemoglobin bound to carbon dioxide (CO2CO_2) on its globin chains, transporting approximately 20%20\% of blood CO2CO_2.

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Erythropoietin (EPO)

A hormone released mainly by the kidneys in response to hypoxia that stimulates red bone marrow to produce erythrocytes.

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Pernicious Anemia

An autoimmune condition targeting stomach parietal cells, preventing the production of intrinsic factor required for vitamin B12B_{12} absorption.

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Sickle-Cell Anemia

A genetic disorder caused by a single amino acid mutation in beta-globin (HbSHbS), causing red blood cells to deform into a sickle shape, block vessels, and rupture easily.

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Vascular Spasm

The initial step of hemostasis in which smooth muscle in the damaged blood vessel wall contracts to narrow the vessel and limit blood loss.

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Platelet Plug Formation

The second step of hemostasis where platelets aggregate at exposed collagen via von Willebrand factor and release chemicals (ADPADP, serotonin, thromboxane A2A_2, and Ca2+Ca^{2+}) to recruit more platelets.

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Intrinsic Pathway

A slower coagulation pathway triggered by contact with collagen or activated platelets inside the damaged blood vessel.

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Extrinsic Pathway

A rapid coagulation pathway triggered by Tissue Factor released by damaged cells outside the blood vessel.

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Plasmin

An active fibrin-digesting enzyme formed from plasminogen that dissolves blood clots during fibrinolysis.

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Thrombus

A blood clot that develops and remains attached to the intact wall of a blood vessel.

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Embolus

A blood clot or intravascular mass that breaks free from its site of origin and travels through the bloodstream.

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Thrombocytopenia

A condition defined by a diagnostic platelet count below 50,000/μL50,000/\mu L, leading to petechiae and spontaneous bleeding.

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Agglutinogen

A surface antigen on red blood cells (such as A, B, or D) that determines blood type and can react with specific antibodies.

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Agglutinin

An antibody dissolved in plasma (such as anti-A or anti-B) that causes clumping (agglutination) when binding to matching red blood cell antigens.

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Erythroblastosis Fetalis

Hemolytic disease of the newborn caused when maternal anti-Rh IgGIgG antibodies cross the placenta in a subsequent pregnancy to destroy Rh+Rh^+ fetal red blood cells.

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Neutrophils

The most abundant leukocytes (50–70%50\text{--}70\% of WBCs), serving as highly phagocytic, short-lived responders in innate immunity.

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Monocytes

Agranular leukocytes (3–8%3\text{--}8\% of WBCs) that migrate from blood into tissues to transform into chief phagocytic cells known as macrophages.

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Natural Killer (NK) Cells

Cytotoxic innate lymphocytes that identify and destroy target cells missing normal self surface markers without requiring MHC presentation.

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Diapedesis

The process by which leukocytes squeeze between endothelial cells of capillary walls to leave the bloodstream and enter injured tissue.

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Pyrogen

A fever-inducing chemical released by leukocytes or pathogens that acts on the hypothalamus to raise body temperature.

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Immunocompetence

The functional maturation of a lymphocyte allowing it to recognize and bind to one specific antigen.

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Self-Tolerance

The state in which mature lymphocytes are rendered unreactive to the body's own self-antigens.

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Major Histocompatibility Complex (MHC)

A set of cell surface proteins used for self-recognition; MHC-IMHC\text{-}I occurs on all nucleated cells, whereas MHC-IIMHC\text{-}II occurs exclusively on antigen-presenting cells.

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Helper T Cells (THT_H)

CD4+CD4^+ T lymphocytes that direct immune responses by activating B cells, T cells, and driving cell proliferation.

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Cytotoxic T Cells (TCT_C)

CD8+CD8^+ T lymphocytes that directly attack and destroy infected or cancerous body cells presenting foreign antigens on MHC-IMHC\text{-}I.

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IgM

The pentameric antibody class produced first during a primary immune response, effective at complement activation and agglutination, but incapable of crossing the placenta.

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IgG

The most abundant plasma antibody class, dominant in secondary immune responses, capable of crossing the placenta and granting passive immunity.

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IgE

An antibody class that binds mast cells and basophils, triggering histamine release responsible for allergic reactions, asthma, and anaphylaxis.

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Active Immunity

Long-lasting immunity established when an individual's own B and T cells encounter antigens and generate an active response with immunological memory.

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Passive Immunity

Short-term immunity conferred by receiving pre-formed antibodies from another source without activating memory cell production.

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Opsonization

The process of coating a pathogen with antibodies or complement proteins to enhance its recognition and phagocytosis by leukocytes.

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Primary Lymphoid Organs

Anatomical sites where lymphocytes originate and mature, consisting of red bone marrow for B cells and the thymus for T cells.

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Secondary Lymphoid Organs

Tissues where mature, immunocompetent lymphocytes encounter antigens and launch adaptive responses, including lymph nodes, spleen, and tonsils.