Midterm 1 Flashcards

(94 cards)

1
Q

Nervous system

A

part of an animal that coordinates its actions by transmitting signals to and from different parts of its body

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2
Q

immunity

A

combination of all mechanisms used by the body as protection to environmental agents that are foreign (“non-self”) to the body (“self”)

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3
Q

Immune system

A

a series of obstacles to limit and inhibit pathogen entry and then attack and destroy those organisms once they enter the body

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4
Q

foreign invaders

A

viruses, bacteria, fungi, parasites (amoebae, worms, plasmodium, etc)

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5
Q

internal corruption

A

dead tissue, tumors

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6
Q

neuroimmunology

A

field combining neuroscience, the study of the nervous system, and immunology, the study of the immune system

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7
Q

intracellular chemical messenger

A

a hormone; a chemical substance, a molecule, that is secreted by one cell of the body and modifies the function of another cell of the body.

primary vehicle for intercellular communication

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8
Q

neurocrine signaling

A

synaptic transmission

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9
Q

neurotransmitters

A

chemical messengers secreted by neurons that diffuse across the small gap to the target cell

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10
Q

endocrine signaling

A

happens when 1 cell (specialized cell or many nonspecialized endocrine cells that can secrete substances which are hormones (messengers which operate in the endocrine system)), and these hormones are released first into interstitial. From this, they diffuse into the bloodstream and carried to distant organs where they exit the circulation. If there is a target cell which expresses specific receptor at plasma membrane, it will initiate intracellular events leading to a specific response of the target cell.

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11
Q

hormones

A

chemical messengers secreted by endocrine cells into the blood. carried with blood to distant targets.

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12
Q

Receptors

A
  • binding of receptor with agonist produces a conformation change in the receptor itself.
  • cells lacking specific receptors do not recognize the hormones cytokine. binding of a hormone/cytokine to the specific receptor initiates downstream signaling leading to a specific response.
  • location of receptors are tissue/organ specific
  • receptor distribution across the immune and neuronal systems forms the basis for communication
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13
Q

Autocrine signaling

A

when the cell releases a hormone but also experiences in response to the presence of this hormone by itself. major regulator of immune cells.

cell is targeting itself.

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14
Q

paracrine signaling

A

major feature: hormone doesn’t enter into circulation. the producer releases hormone and the hormone travels short distance to activate receptors on neighboring cell.

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15
Q

neuroendocrine signaling

A

happens when neurons spill neurotransmitters (operating in narrow space in synaptic cleft) that are specialized and release them into circulation. These neurotransmitters then act in endocrine fashion (travel in blood and activate receptors on distant target cells)

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16
Q

neurohormones

A

chemical messengers secreted by neurons into the blood for action at the distant targets.

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17
Q

extravasation

A

moving of the lymphocytes from bloodstream into the tissue. instead of hormones, leukocytes bring themselves into specific area of the body, where they can either release specialized intracellular messengers called cytokines.

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18
Q

cytokines

A

hormones operating in the immune system; usually small peptides. can be released by any type of cell, not just immune cells in response to insult.

  • hydrophilic, membrane impermeable
  • typical feature of cytokines: modification of gene expression
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19
Q

antigen presenting cell/juxtacrine or direct signaling

A

major type of communication and recognition of antigen.

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20
Q

Janus kinase (JAK)

A

protein kinase (many cytokines work through activation of JAK); signal transducer and activator of Transcription (STAT) pathway is a common signaling pathway used by many cytokines

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21
Q

cytokine receptors

A

multiple cytokines can cross-link the same receptor

a single type of receptor can activate multiple downstream signaling cascades

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22
Q

pleiotropy

A

cytokine pleiotropy is the ability of a cytokine to exert many different types of responses (often on different cell types)

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23
Q

redundancy

A

cytokine redundancy refers to the fact that different cytokines can induce similar signals

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24
Q

microbiota

A

a cohort of microorganism which inhibit animal or human bodies

  • vast majority are beneficial (commensal). Hosts evolved to require colonization by beneficial commensals.
  • can become pathogenic if they translocate into the body.
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25
innate immune system
barriers to pathogens. first responders after barrier is breached and mount the first response to localize and eradicate these harmful invaders before it spreads to the whole body and kills the host. Nonspecific! - physical: skin, mucosal membranes - mechanical: flow of fluids, sweat, mucus, saliva - chemical: fatty acids, acidity, antimicrobial peptides - biological: normal/commensal microbiota
26
epidermis
where living cells reside. very dense layer that creates a physical barrier
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dermis
where most cells reside. these cells are macrophages, natural killer cells, dendritic cells, etc
28
innate immune cells
epithelial barriers, phagocytes, dendritic cells, complement, NK cells
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adaptive immunity
2nd response; activated when innate fails to eradicate and contain foreign pathogen. activation takes a long time. Specific to the pathogen! - as a result of activation, two types of effector signals are formed: antibodies and mounts a response against pathogens through effector T cells.
30
T lymphocytes
through multiple steps of activation maturation information, they confront pathogens or infected cells through producing lytic granules to physically kill them.
31
lymphatic system
co-exists with blood, necessary to pick up the fluid which accumulates in different tissues as a result of fluid exchange during blood movement through the tissues, and lymphatic picks up the residual fluid, which leak from the blood capillaries (into the tissues), and returns it into circulation (blood) - passive; it is pushed through the blood due to contraction of smooth muscle cells surrounding the capillary and the contraction of skeletal muscles
32
capillary bed
penetrated by lymphatic capillaries which collect left over fluids moved into tissue and not reabsorbed by capillaries. move fluid back into circulatory system.
33
Specific organ of lymphatic system
lymph-nodes - an enlargement.
34
Blood-lymph circulatory system
lymphatic capillaries are near blood capillaries. they collect lymph fluid (plasma that leaks out of the cardiovascular capillaries) and proteins from the tissues. - pathogens and their antigens are also transported from tissues via lymphatic vessels to the lymph nodes where they encounter immune cells. - lymph moves in one direction toward the heart, which prevents pathogens from flowing through the entire body.
35
lymphoid tissues
immune cells tend to accumulate in the lymphoid organs; they develop (arise) in the primary lymphoid organs, and they interact with the foreign antigens in the secondary lymphoid organs
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primary lymphoid organs
bone marrow and thymus
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bone marrow
adult hematopoietic cells arise from pluripotential bone marrow stem cells - site of B cell development
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thymus
site of T cell development (t cells are "educated" to distinguish between "self" and "non-self")
39
secondary lymphoid organs
spleen and lymph nodes
40
spleen
filters and collects antigens from blood | - harbors cells of innate and adaptive immunity
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lymph nodes
- placed throughout the body; are most densely distributed towards the center of the body, particularly around the neck, intestines and armpits - filter lymph and collects antigens from tissues - place where T cells can interact with antigen-presenting cells - place of T cell clonal expansion
42
hematopoiesis
development of immune and other blood cells from a small population fo stem cells known as hematopoietic stem cells
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erythropoiesis
production of erythrocytes, RBC
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leukopoiesis
production of leukocytes, WBC
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leukocytes
any WBC, which plays role either in innate or adaptive immunity
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phagocytes
process by which a cell engulfs a solid particle or another cell
47
phagocytic
a type of cell capable of engulfing and absorbing bacteria and other small cells and particles by phagocytosis
48
Cells of Myeloid Lineage
major cells of innate immunity; highly phagocytic (neutrophils, monocytes, macrophages, dendritic cells) major are involved in immediate protection against most pathogens - other: granulocytes (eosinophils, basophils, mast cells) other are involved in defense against parasites and allergic reactions
49
Cells of Lymphoid lineage
B lymphocytes, T lymphocytes (T cells), Natural killer cells (NKs), Natural Killer T cells (NKT)
50
B lymphocytes (B cells)
major effector function: secretion of antibodies (Ab), proteins which bind pathogens or their toxic products in the extracellular spaces of the body
51
T lymphocytes (T cells)
major effector function: secretion of lymphokines to direct immune response (helper T cells, CD4+) or destroy infected cell (cytotoxic T cells, CD8+)
52
Natural Killer Cells (NK)
lymphoid in origin, but part of the innate immunity that recognizes and kills pathogens or infected cells by releasing lytic enzymes
53
Natural Killer T Cells (NKT)
both innate (kill pathogens) and adaptive mechanisms (secrete cytokines)
54
Cluster of Differentiation (CD)
cell surface protein typically expressed on the cells of the specific lineage and type. each molecule is assigned a different number (think: CD1, CD2, CD3, etc). -functionally different leukocytes has specific CD expression pattern (example: CD4+ = T helper cells; CD8+ = cytotoxic T cells)
55
vasodilation
capillaries become wider and more blood flow that surrounds damaged area
56
inflammation
defensive process that a living body initiates against local tissue damage; protective response and serves to bring defense and healing mechanisms to the site of injury
57
inflammation triggers
physical agents: burns, trauma, radiation chemicals: drugs, toxins, caustic substances microbial infections: bacterial, viral, fungal immunologic reactions: autoimmunity
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PAMPs
pathogen-associated molecular patterns - evolutionally conserved structures expressed on the surface of many pathogens (proteins, lipids, nucleic acids, carbohydrates)
59
DAMPs
danger associated molecular patterns. - tissue damage/necrotic cell products (heat-shock proteins (HSP), uric acid crystals, aggregated peptides, ATP) - misfolded proteins (e.g. amyloid beta)
60
PRRs
PRRs recognize PAMPs or DAMPs. Each PRR recognizes a DAMP or PAMP that is shared by many different damaged cells or pathogens -> broad recognition since there is a limited collection of molecular patterns that can be recognized. - PRRs expressed by innate leukocytes, macrophages, and mast cells in peripheral tissues.
61
Toll-Receptor
common type of pathogen recognition receptor.
62
innate phagocytes
resident: macrophages, dendritic cells recruited: neutrophils, monocytes - engulf and destroy pathogens - capable of engulfing particles larger than themselves - pseudopods
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pseudopods
fine sheets of membrane that macrophages extend to engulf cells
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chemotaxis
movement of a motile cell or organism, or part of one, in a direction corresponding to a gradient of increasing or decreasing concentration of a particular substance.
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chemoattractants
small soluble molecules which attracts motile cells of a particular type
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monocytes
differentiate into macrophages in inflamed tissues | - not actively phagocytic; provide help to other macrophages by expansion to macrophages
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granulocytes
neutrophils, basophils, and eosinophils; short lived phagocytes
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ELAM1
epithelial cell adhesion molecule-1
69
selectins
carbohydrate-binding proteins
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chemokines
any cytokines with function of chemoattractants, including attracting WBC (leukocytes) to sites of infection/tissue damage
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acute phase of inflammation
characterized by the rapid influx of blood granulocyte, typically neutrophils, rapidly followed by monocytes - monocytes proliferate and mature into inflammatory (M1) macrophages - phagocytosis is carried on by recruited and resident phagocytes - Phase 1 and 2
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Resolution phase of inflammation
the usual outcome of the acute inflammatory program is successful resolution and repair of tissue damage - phase 3 and 4
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principal phagocytes
neutrophils and macrophages share powerful phagocytic capacity and elaborate intracellular killing machineries
74
neutrophils
- rapid increase in numbers during acute phase response - found only in inflamed tissues - single mature form - short-lived (6-24 hrs), die after phagocytosis - form pus (dead neutrophils and debris)
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macrophages
- slightly increased levels during inflammation - found in healthy tissues - several mature forms - long-lived, survive after phagocytosis
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insults
metabolic deprivation, toxicity, pathgens, trauma
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meninges
three thin layers of tissue that cover and protect the brain and spinal cord. the meninges comprise of the: - DURA MATER - ARACHNOID MATER - PIA MATER
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CSF
produced in the choroidplexus in the ventricles of the brain and flows between the arachnoid and the pia maters of meningeal layers. - provides mechanical support, regulates ion composition, and maintains chemical stability
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Blood-brain barrier (BBB)
highly selective semipermeable border of endothelial cells that prevents solutes in the circulating blood from non-selectively crossing into the extracellular fluid of the CNS. Protects CNS (brain and spinal cord) from the toxins and pathogens that may be traveling through the blood capillary network. - formed by tight junctions between endothelial cells liming cerebral micro-vessels, in addition to glial cells
80
Glia limitations
astrocyte end "feet" that cover the vessels that go to the brain and provide barrier between meninges and PIA MATER - separates the brain parenchyma from the CSF/perivascular spaces and plays a major role in compartmentalizing CNS immune reactions
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Pericytes (PC)
contractile cells that control blood flow
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BCSFB
formed by tight junctions between epithelial cells at the choroid-plexus, endothelial cells of the veins, and venules within the subarachnoid space, and the epithelial cells of the arachnoid mater
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olfactory system
bypasses the cellular barriers of the CNS and provides a direct portal from the nasal cavity to the olfactory bulb within the brain. this is where the pathogen breaches CNS to produce infection
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CNS innate system cells
microglia, astrocytes, macrophages
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what are not found in the CNS innate immune system
NO neutrophils, no NK cells, no antigen-presenting DCs, machrophages are restricted to perivascular space
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microglia
keeps surveillance for damage or infection. phagocytic scavenger that is highly motile; responsive to injury, infection, and neuronal electric activity; synaptic pruning; removal of dead cells by phagocytosis. - only hematopoietic cells found in parenchyma of the CNS - unique myeloid population - derived from yolk sac during embryogenesis - in parenchyma, sustained by proliferation of resident progenitors independent of blood cells - related to resident tissue macrophages - activation is accompanied by morphological and functional changes (phagocytic macrophages)
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astrocytes
derived from neuroepithelial stem cells like neurons. - ensheathe vasculature and synapses - regulate neuronal excitability and synaptic transmission - protects from "excitotoxicity" by removing excess of neurotransmitters (glutamate) and buffering K+ - exclusively convert glutamate to glutamine - secrete extracellular matrix proteins - implicated in neurogenesis and cell migration - activation is triggered by any alteration in brain homeostasis
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Pro-inflammatory type 1 cytokines
``` interleukin 1beta interleukin 18 interleukin 6 interleukin 17 tumor necrosis factor alpha interferon gamma histamine ```
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anti-inflammatory type 2 cytokines
transforming growth factor beta interleukin 4 interleukin 10
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brain parenchyma
brain tissue composed on neurons and glial cells
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Perivascular space
separates the capillary endothelial cell layer from the astrocytes end feet - believed to play a role in antigen drainage from the CNS parenchyma - largely the CSF, which contains peripheral immune cells
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postcapillary venule
surrounded by a perivascular space
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immune surveillance
theory that the immune system patrols the body to recognize and destroy invading pathogens and host cells that become cancerous
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antigens
molecules from pathogens; move from the CSF compartment to mandibular and deep cervical lymph nodes by exiting through perineural pathways (olfactory and optic nerves) and lymphatic vessels traversing the dura mater into lymphatic vessels that reside outside the CNS.