Histology Flashcards

(34 cards)

1
Q

What are the 3 main functions of blood?

A

Transport and Distribute gases, immune response, hormones.

Homeostatic regulation of temp and osmotic balance

Clotting and Healing vascular wall.

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2
Q

What is the composition of plasma?

A

92% water

7% Protein

1% other solutes (nutrients, electrolytes)

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3
Q

What is the difference between plasma and serum?

A

Serum is coagulated plasma and so the values found from both are technically different.

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4
Q

What is the Plasmalemma?

A

The membrane of a red blood cell. Peripheral and Integral membranes anchor and organize the cytoskeletal proteins.

Peripheral on inside. Integral in membrane

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5
Q

What is the function of the peripheral protein spectrin?

A

They are cytoskeleton that can attach and reconnect to allow the membrane to change shape in small capillaries.

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6
Q

Thalassemias?

Hemoglobinopathies?

A

Genetic disorders related to the underproduction of hemoglobin

Genetic disorders related to dysfunctional hemoglobin

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7
Q

What is Polycythemia?

Erythrocytosis

A

Increase in RBC count, caused by a variety of factors: environmental adaptation (decrease in atmospheric pO2) physiological or pathological.

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8
Q

Describe Platelets (Thrombocytes)

A

Membrane bound cell fragments

A nuclear with sparse mitochondria

Have Glycocalyx that lines the extracellular membrane to allow sticking.

Filled with different granules

Outer cytoplasm has complex intracellular arrangement to facilitate rapid degranulation.

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9
Q

What is the process of platelet clotting?

A

Primary aggregation: Glycogcalyx allows platelets to adhere to substrate or damage

Secondary aggregation: release of glycoproteins and ADP to induce more aggregation

Blood coagulation: Released granules

Clot retraction: clot contracts due to activity of platelet actin and myosin

Clot removal: growth of new tissue repairs damage.

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10
Q

Thrombocytopenia purpura?

Hemophilia?

Thrombophilia?

A

Circulating platelet function is compromised (causes pitichiae)

Genetic disorders in the function of clotting factors

Disorder that increases the risk of thrombosis.

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11
Q

Which WBC are granulocytes and which are Agranulocytes?

A

Granulocytes: Neurtrophil, Eosinophil, Basophils

Lymphocyte, Monocytes

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12
Q

How do you differentiate Neutrophils

Eosinophils

Basophils Histologically?

A

3-5 lobes: Granules are less dense and stain lightly pink

Bi-lobed nucleus: granules stain pink/red and there are more than neutrophils

Bi-lobed or S-shaped nuclei: with dark purple granule- have heparin, GAGs, Histamines
(Involved in allergic reactions with mast cells in type 1 hypersensitivity)

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13
Q

What are the histological Characteristics of:

Lymphocytes

Monocytes

A

Lymphocytes: Smallest diameter, spherical nucleus, maybe slight indentation. Thin ring of basophilic cytoplasm.
(T, B and NK cells) (Need to be presented antigen for T and B cells)

Monocytes: Indented or C-shaped nucleus with basophilic cytoplasm. Granules are present but very small.
(Many become antigen presenting cells)

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14
Q

Explain Leukocyte Extravasion

A
  1. Macrophage releases PROINFLAMMATORY CYTOKINES IL-1 and TNF-a. Signals selectins
  2. Neutrophils bind to selectins to loosely adhere
  3. Other cytokines express integrins on the neutrophil and ICAM-1 on the endothelial surface
  4. Integrins provide firm adhesion
  5. Attracted by local injury factors neutrophils become motile and migrate by DIAPEDESIS between loosened cells.
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15
Q

What is Anaphylaxis?

A

Rapid degranulation of mast cells and basophils regulating in vasodilation in many organs that drop blood pressure.

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16
Q

Explain the embryology of the sites of hemopoiesis

A

Yolk Sac first

Liver and Spleen from 3 to 6 months gestation

Bone marrow: tibia and femur as kid. Ribs sternum and vertebrae later on.

17
Q

What is the make up of Red Marrow?

A

hematopoietic cords: Cell lines, maturing cells, and more hematopoietic cells

Reticular tissue to support mesh work of hematopoietic cords

Sinusoid also capillaries- lined by discontinuous endothelium (the holes let cells easily leave to mature)

Adipocytes (increases with age)

18
Q

What are pluripotent stem cells?

A

Stem cell that can give rise to any of the 7 blood cells.

First differentiate to CMP (common myeloid cell) or CLP for lymphoid stem cells

CMPs become Erythrocytes or Thrombocytes

CLP for Lymphoid or grulocytes

19
Q

What is cellularity?

A

Percentage of marrow that is comprised of active hemopoietic tissue vs. adipose tissue.

20
Q

Erythropoiesis?

Go over this in the notes

A

Differentiation of proerythroblast from CMP (or MEP from research) driven by erythropoietin

Nucleus is ejected making a reticulocyte that still has some ribosomal bundles. Within a few hours that become mature erythrocytes.

RBCs are pushed into the sinusoidal capillaries because of the holes in them.

21
Q

Explain Thrombopoiesis

A

Differentiation of megakaryoblasts from the CMP (MEP) driven by thrombopoietin

Large cells with endomitosis rounds that divide DNA without dividing the membrane.

They then bud off those pieces of DNA that are dropped into the bloods using proplatelets that extend into sinusoidal capillaries

22
Q

Explain Granulopoiesis

A

Differentiation of Granulocytic progenitors (myeloblasts) driven by G-CSF

Promyelocyte have Golgi and RER with small granules

Myelocyte — Metamyelocyte have the specific granules of the granulocytes

Band Stage — an intermediate stage in which the nucleus has not completely formed its polymorphic shape.

23
Q

Explain how neutrophil numbers can rise so quickly?

A

Marginating cells that are on the endothelium but not in the blood that are ready to go. There are also many in storage or ready to differentiate.

24
Q

Explain Monocytopoiesis.

A

Differentiation of monocytes progenitor cell and monoblasts driven by M-CSF

Promonocyte have slight indentation and stains slightly basophilic.

25
Explain Lymphopoiesis
Differentiation of a lymphoblast from CLP complex They become pre-lymphocytes that can then be matured in different places. T-cells go to Thymus NK cells go to secondary lymph or stay in Bone marrow. B-cells stay in the bone marrow to mature
26
Thrombocytopenia
Thrombocytopenia purpura is a platelet function problem ie autoimmune. Ineffective megakaryopoiesis is a disruption or reduction of produced platelets.
27
What are Primary and secondary structures?
Bone marrow and Thymus are primary Mucosa-associated lymphoid tissue (MALT) Lymph nodes Spleen
28
Explain Lymphatic tissue generally?
Use reticular CT as support (except thymus) Have lymphocytes, palms cells, and macrophages.
29
Explain positive and Negative Cortex/Medulla selections
Positive in Cortex: MHC is bound by lymphocytes and so they move into medulla to mature Negative in Medulla: If the cell overreacts to self-antigen then the T-cell is signaled for apoptosis. If not it is released into the blood as a mature T-cell. Final step is to retain CD4 as a Helper T-cell or retain CD8 as a cytotoxic T-cell. (Only 2% of cells survive selection)
30
Where is MALT (mucosa-associated lymphoid tissue) found?
Diffuse in mucosa (in lamina propria) of GI, respiratory, and UG systems. Or more concentrated in Lympoid nodules. With primary and secondary nodules. Peyer’s Patches, Tonsils, vermiform appendix Primary nodules have no germinal center and so no active immune response happening
31
Explain Adenoids
Chronic inflammation and hyperplasia of the pharyngeal tonsils, which can obstruct the pharyngeotympanic tube and lead to middle ear infections
32
What are the parts of lymph nodes?
Capsule with trabeculae Cortex (superficial cortex) *Have lympoid nodules Paracortex: (Has place for cells to migrate into lymph nodes and then move to nodules.) Medulla (middle): Has exit sinuses that drain into efferent lymphatic vessels.
33
What are the functions of the spleen?
Filter effete red blood cells Site of immune responses Reservoir for blood and its cells Site of fetal hemopoiesis
34
What is the make up of the spleen?
Capsule with trabeculae White pulp: 20% of pulp. Where immune response occurs Red Pulp: 80% of pulp. For blood filtration.