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Physiology of bloodGyöngyi Karcsúné Dr. Kis

Evening seminar

LOs 8-13., highlighted, bold red color

#8 Identify the protein fractions of blood plasma, explain the method (electrophoresis) used for their measurement. Give 1-1 example from each fraction.

#9 Describe the mechanism of blood sedimentation, the method of its measurement, significance and normal value.

#10 Provide the definition of reticulocyte, its staining and the significance of reticulocyte count. Erythropoietin: production (kidney), trigger, function.

#11 Provide the definition of direct and indirect bilirubin. Urobilinogen (UBG), and the significance of its detection in the urine.

#12 Describe the role and structure of immunoglobulins and their subtypes and functions.

#13 Describe the antigens and the circulating antibodies (Landsteiner-rules).

#14 Explain the adhesion, aggregation and activation of thrombocytes.

#15 Describe the extrinsic pathway. Describe the intrinsic pathway and the contact phase.

#16 Expound the activation and regulation of the plasmin system.

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##PlasmaPlasma proteinsproteins� 60-80 g/l

� > 70 kDa

� Non-diffusible

� Mainly glycoproteins (polysaccharide chain, hexose, frucose), [except albumin]!

� Functions:� Colloid-osmotic pressure (albumin)

� Transport

� Buffer (pH regulation)

� Proteolytic enzymes (e.g. blood clotting, complement system)

� Anti-proteolytic proteins and protease inhibitors

� Enzymes

� Immunoglobulins

� Modulators and acute phase proteins

� Tumour markers

Plasma/serum proteins - quantitative measurement� Routine: biuret test

� Normal: 60-80 g/l, plasma fibrinogen +2-6 g/l

� Hyperproteinaemia: dehydration - renal fluid loss; multiple myeloma

� Hypoproteinaemia: protein loss - haemorrhage, burn; malnutrition; malabsorption; hepatic diseases – decreased protein production; infection – increased protein catabolism

� Dysproteinaemia: abnormality of the protein content (ratio)

� Disease � protein content/alteration can be characteristic

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Plasma protein - electrophoresis

Background:

� Alkaline environment: negative (pH=8.6)

� Traveling towards anode (electromotive force)

� Speed: depends on charges, molecular weight

� AAs (glutamic acid, aspartic acid)

� Various mediums: paper, agarose (gel), polyacrylamide (gel) –separation

Plasma protein - PAGE

Workflow

SDS-PAGE

(www.bio-rad.com)

• Molecular filter (gel) (separates 20

fractions)

• Staining:

• Silver (small quantities)

• Oil-Red, Sudan-black

(lipoprotein)

• Periodic acid-Schiff

(glikoprotein)

• Specific substrates and enzymes

• Measurement: densitometry

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##ExamplesExamples

Albumin

� 35-50 g/l

� Albumin/globulin diagnostic importance (1,5-2,5); decrease: hepaticdisfunction, diarrhea, malnutrition

Antitrypsin

� α1- globulin

� 2-4 g/l

� Inhibition of proteolysis in inflammatory processes

� Absence: liver damage

Haptoglobin

� α2- globulin

� Binding free hemoglobin

� 0,5-2,2 g/l

� Acute phase protein

Transferrin

� Β-globulin

� Transport of iron ions

� 2-4 g/l

� Increased level in iron deficiency

Other methods 1.Radial immunodiffusion (Mancini):

Ag-At binding, specificity, quantitative

Agarose plate

standard protein solutions �

calibration

Precipitation rings, diameter and area

proportional to the Ag concentration

Immunoelectrophoresis:

Agarose

Specificity

Semiquantitative

Rocket elektrophoresis:

Quantitative

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Other methods 2.

� RIA

� ELISA

� Turbidimetry, nephelometry

� Measurement of biological activity

Specific plasma proteinsCYTOKINES:

-Low molecular weight

-communication of leukocytes

-Soluble, multifunctional mediators

-Autocrine, paracrine, endocrine effects

-Pleiotropy, redundancy

-Synergist, inhibitory, modulator

1. Interleukins (IL)

2. Interferons (INF) (antiviral, tumour/autoimmun--treatment)

3. Tumour necrosis factor (TNF)

4. Transforming growth factor (TGF) (tumours, tissue regeneration)

5. Colony-stimulating factors (CSF) (bone marrow, cell proliferation)

6. Adipokines (produced by visceral fat)

ACUTE PHASE PROTEINS

CRP (C-reactive protein)

-Binds C polysaccharide in cell wall of Pneumococcus

-Liver

-1-8 mg/l

-Mediators: cytokines

-Swelling of bacterial wall

-Improves uptake of necrotic remnants

-Activates complement system (classic pathway)

-Immunomodulatory

Serum-amyloid A (SAA) & P (SAP)

-Different isoforms

-Apolipoprotein (transport)

Procalcitonin

-Marker of severe sepsis caused by bacteria

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#Erythrocyte sedimentation#Erythrocyte sedimentation

� inhibited coagulation (e.g. citrate, EDTA), gravitation

� 3 phases:

� Aggregation: slow, proteins have important role � aggregate (rouleauxformation)

� Precipitation: aggregates precipitate in the plasma, faster

� Clustering: aggregates sank, slow

� Normal values:

� Male: 2-6 mm/h

� Female: 8-10 mm/h

� Non specific!!!

Erythrocyte sedimentation rate (ERS)

� Westergren

� Na-citrate, EDTA

Faster sedimentation (>normal value)

Age, anaemia, pregnancy, macrocytosis, inflammation, tumour

Slower sedimentation (<normal value)

Hematocrit (male!), microcytosis, hypogammaglobulinaemia, spherocytosis

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##ReticulocyteReticulocyte

� RBC precursor

� Contains: RNA, haemoglobin (34 %), network of granules or filaments (residual RNA and organelles)

� Bone marrow (<1 % RBCs) (diapedesis)

� Immature � 1-2 days � mature erythrocyte

Reticulocyte count

� Importance: erythropoietic activityof bone marrow

� Necessity: differential diagnosis foranaemia, follow-up cares: bonemarrow transplantation, chemotherapy

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Reticulocyte count methods

1. Brillant cresyil blue or methylene blue staining � light microscope(see lab practice!) (Hb, RNA precipitate)

(time-consuming, unaccurate)

2. Automatic methods:� Larger number of counted cells� Faster� Reproducible results� Less possible error1. Electric resistance -- Coulter- counter

As each particle enters the aperture, it has essentially displaced a volume ofelectrically-conductive fluid equal to its own volume, and the baseimpedance is therefore modulated by an amount proportional to thevolume of the particle. This results in an electrical pulse of short durationbeing created by each particle; the height of the pulse being essentiallyproportional to the volume of the particle. The pulse may be measuredas a change in resistance, current or voltage across the electrodes.(ThermopediaTM)

2. Flow cytometer� Optical� cells are forced one at a time through a focused light beam� Labelling with fluorescent dye, e.g. auramin-O, thiazole orange (TO), 488 nm

Changes in reticulocyte count

� > : increased RBC production (due to blood loss, anaemia)

� < : decreased RBC production (anaemia (pernicious, aplastic, iron deficiency), radiation, infection, bone marrow deficiency)

� Result might interfere with:

� drugs for Parkinson’s disease, rheumatoid arthritis, fever, malaria, chemotherapy

� Radiation

� Antibiotics

� Pregnancy

� Blood transfusion

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##ErythropoetinErythropoetin

� Glycoprotein (cytokine), 34 kDa

� Isolated in 1977

� Production:

Kidney (85-90 %, peritubular fibroblast-like interstitial cells in cortex

and outer medulla – site of O2 consumption!)

Liver (10-15 %)

� Hypoxia (kidney) � tissue hypoxia inducible factor-2 (HIF-2) is constitutively synthesized and no longer degraded � EPO gene HRE (hypoxia response element) �� EPO

� Other stimulators: hypoxia non-renal sensors, adrenalin, noradrenalin, prostaglandins, spherocytosis

Haase VH. Regulation of erythropoiesis by hypoxia-inducible factors, Blood Rev., 2013

HIF-EPO-Ironmetabolism

Renal EPO-producing cells

Divalent metal transporter

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ferroportin

Transferrin complex

(hepcidin promotes ferroportin degradation)

more iron is released from enterocytes,

hepatocytes and RES cells

HIF-regulated genes

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EPO receptor on erythroid progenitor cell

EPO non-erythroid effects

Wang et al., Erythropoietin, a Novel Versatile Player Regulating Energy Metabolism beyond the Erythroid System, Int J Biol Sci, 2014

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EPO as a PED

� most widely used PED (performance-enhancing drug)

� Stroke, thrombus, heart attack

#Bilirubin#Bilirubin

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Bile pigment

� Haemoglobin (80 %), tissue haemoproteins (myoglobin, cytochromes, enzymes)

� Antioxidants effects

� Non-conjugated bilirubin: van den Bergh-reagent + alcohol discoloration �indirect reaction � indirect bilirubin

� Not filtrated in kidney, no presence in urine (albumin)

� Increased RBC degradation, haemolysis, haematoma � glucuronide production ↓�

Hyperbilirubinemia: > 40 µmol/l (sclera, skin yellowish, icterus, Kernicterus – blood-brain barrier!)

� Blood contains indirect bilirubin (5-17 µmol/l)

� Conjugated bilirubin: direct bilirubin

� hepatocyte dysfunction (direct bilirubin returns into sinusoidal blood) � water soluble, hyperbilirubinemia � filtrated in kidneys � presence in urine

Urobilinogen

� 80-90 % oxidation to stercobilinogen, excretedwith feces

� 10-20 % blood stream to liver and kidney

� Kidney: filtrated, urine

Prehepatic: haemolysis, haematoma,

hereditary or acquired haemolytic

disorders

Intrahepatic: Gilbert-disease (transport),

decreased bilirubin uptake or conjugation

(benign), hepatocyte damage,

inflammation

Posthepatic: obstuction of bile duct

(tumor, stone, inflammation)

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White blood cells(leukocytes)

May-Grünwald-Giemsa staining

Flow-cytometry (marker of cell

surface)

� Number: 5-8 000 cells/µl

� Haematopoetic stem cell, HSC

� Bone marrow, blood stream, lymphatic system, organs

� Quantitative blood test:

� leukocytosis(↑), leukopenia(↓)

� Qualitative blood: percentage of the leukocyte types

Types of leukocytes

� NEUTROPHIL - 50-70%

� diameter: 10-12 μm

� nucleus: segmented (multiple lobes)

� granules: small, poorly stained

� lifespan: hours (spleen-tissue: days)

� targets: bacteria, fungi

� Phagocytosis

� EOSINOPHIL - 2-4%

� diameter: 10-12 μm

� nucleus: two lobes

� granules: large, hematoxylin-eosin staining

� lifespan: 1-2 weeks (hours in circulation)

� Targets: parasites, allergic reactions

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� BASOPHIL - < 1%

� diameter: 12-15 μm

� nucleus: 2 or 3 lobes

� granules: strong basophil staining (blue)

� lifespan: several hours-days

� Histamine release during inflammation and allergy – anaphylaxia

� LYMPHOCYTE - 20-40%

� diameter: 7-8 μm

� nucleus: non-central, round

� Life-span: weeks-years

� B-cells: antibody production (plasma cell) – humoral immunity

� T-cells: destroying cells infected by viruses (and tumour cells) – cellularimmunity

� NK (Natural Killer) cell: large lymphocyte, non-specific cellular immunity

� MONOCYTE - 4-8%

� diameter: 15-20 μm

� nucleus: bean shape

� phagosoma in the cytoplasm

� lifespan: hours-days in circulation, in tissue: macrophag (without activationmonths-years), activated by cytokins, chemoattractants

� phagocytosis (microbes, tissue debris), antigen presentation

� Tissue macrophages (Histiocytes) (reticuloendothelial system/monocyte-macrophage cell system):� Dendritic cells (skin, mucous epithelium)

� Kupffer cells (liver)

� Microglia (brain)

� Osteoclast (bone)

� Langerhans cell (skin, mucosa)

� Alveolar macrophages (lung)

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Phagocytosis� Phago=devour, cyto=cell, sis=process

� Engulfing and destruction of particulate matter

� Neutrophil granulocyte, monocyteAutophagy:

Nobel Prize in Physiology or Medicine (Ohsumi, 2016)

- new type of vesicle (autophagosome) transporting cellular cargo to the

lysosome for degradation

- controls important physiological functions where cellular components

need to be degraded and recycled

- Fuels the renewal of cellular components

- essential for the cellular response to starvation and other types of stress

- eliminate invading intracellular bacteria and viruses

- embryo development, cell differentiation, eliminates damaged proteins

and organelles, quality control mechanisms

- Disrupted autophagy has been linked to Parkinson’s disease, type 2

diabetes and other disorders that appear in the elderly

Oxidative burst

Reactive Oxygen Intermediates

Reactive Nitrogen Intermediates

Enzymes

Immune responses

1. Natural (innate) immunity

• First contact with the infectious agents

• No memory

• mechanism: phagocytosis, complement proteins (stimulation of phagocytosis [opsoniation], chemotaxis, cytolysis)

2. Adaptive (acquire) immunity

• Based on the recognition of the antigen

• Cell-based (cytolysis) and humoral immunity (production of antibodies)

• memory (vaccination)

Communication and regulation of leukocytes: CYTOKINES

Inflammation response: Arachidonic-acid derivates

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Natural immunity

� Pathogen-associated molecular pattern (PAMP)(e.g. polysaccharide of bacteria, viral RNA): indicating groups of microorganisms, but not specific ones

� Pattern recognition receptors (PRR): PAMP detection: � Toll-like receptors

� NOD-receptor (intracellular, viruses)

� Mannose-binding lectin

� Cells:� MACROPHAGES

� DENDRITIC CELL

� GRANULOCYTES

� NK CELLS (virus)

� Attachement to the endothelial wall � „rolling”, stepping out to the tissue �

migration

Humoral part of innate immunesystem – complement system

Cascade of proteolytic enzymes

Produced in liver (precursor forms)

3 pathways:

ClassicalLectin

Alternative

Function: � Cytolysis (pore formation in membrane – C5-9)

� Chemotaxis (C5a fragment)

� Opsonisation (C3b, C4b)

� Changing the molecular structure of viruses

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Membrane attack complex

(MAC)

Adaptive immunity

� Antigen presentation in the membrane:

MHC (major histocompatibility complex) � A protein joined to the antigen for cell surface display (HLA- human leukocyte antigen)

� MHC-I � Found in every cells

� High degree of variety, individual differences („marker of my cells”)

� cytotoxic T-cells can recognise (virus infected cells, tumour cells)

� MHC- II � Immune cells (antigen presenting cells)

� Join to antigen fragments digested in lysosomes (e.g. bacteria)

� Helper T cells can recognise

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Immunological „synapse”: MHC/antigen – T-cell receptor

Adaptive immunity – T-cellsHelper T-cell (TH)

� CD4 membrane marker

� its receptor recognizes MHC-II + antigen complex

� type 1: facilitation of further phagocytosis

� type 2: facilitation of B-cells - specific production of antibodies

Cytotoxic T-cell (T-killer, T-effector)

� CD8 membrane marker

� recognizes MHC-I

� virus/tumor cell (apoptosis, perforation of the membrane)

NK-cell: cytotoxic without antigen-specificity (part of innate immunity)

CD = Cluster of Differentiation

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Memory cell

� CD8+/CD4+ or B-cell

� stores the memory of antigens for years

� fast activation and division in the case of new exposition

Regulatory T-cell (suppressor T-cell)

� immuntolerance: active inhibition of response in the case of the antigens of self-tissue and tolerated (non-harmful) others

� central: selection of autoreactive cells in the thymus

� peripheral: demarcation (e.g. brain, eye, joints), inhibitory cytokines (TGF), negative co-stimulation (CD molecules)

γδ T-cell

� receptor consists of γδ subunits instead of the common αβ

� intraepithelial lymphocyte in the mucosa

� recognizing whole proteins without MHC

Adaptive immunity – B-cells

� Plasma cell: antibodyproduction

� Antigen presenting cells

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##ImmunoglobulinsImmunoglobulins

IgG: most common, binds phagocytes (opsonization),

passes placenta

IgM: ancient, initial synthesis

IgA: in mucosa-secreted fluid

IgE: cytophil antibody, binds to basophils and mast cells

IgD: B-cell receptor before antigen exposition

Mediators of immune response

ARACHIDONIC ACID derivates:

ACUTE PHASE PROTEINS

CYTOKINES

(see slide #10)

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##BloodBlood groupsgroups

� ~ 35 blood group systems

� AB0 (& Rh): main types

� Prelevance: A: 42%, B: 9%, 0: 46%, AB: 3%

� Antigens & antibodies (agglutinins):

- antigen – foetal life 6th week

- antibody – postnatal life, day #10

� Development: Bacterial infection (E. Coli - B; Strepptococcus - A)

#ABO #ABO antigensantigens

Bombay: H-antigen misses terminal sugar (fucose) → no more sugars can

bind to it (0 group with other genotype)

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Testing for blood group determination

� Not for paternity testing, only excludes!

� Cross reaction:

� Major test

� Minor test

� Non-compatible blood transfusion:

� Antibody-antigen reaction � hemolysis of donor cells � hemoglobin release, kidneyfailure

agglutination

#Landsteiner #Landsteiner principleprinciple

(Karl Landsteiner, 1900)

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Rh (Rhesus) blood group� Protein antigens, 3 allelic pairs: c/C, d/D, e/E

� D is the only strong antigen – Rh+ blood group

� there is no spontaneous immunization (antibodies)only if:

a. Rh-receives Rh+blood

b. Rh-mother has Rh+ baby (Rh prophylaxis by giving incomplete Rh-antibodiesthat suppress production, unless possibility of erythroblastosis fetalis)

Blood clotting

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#14 Explain the adhesion, aggregation and activation of thrombocytes.

Serotonin

TXA2

ADR

collagen

Primary

adhesion

before

activation

Aggregatio

n of the

activated

platelets

#15 Describe the extrinsic pathway. Describe the intrinsic pathway and the contact phase.

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# 16 Expound the activation and regulation of the plasmin system.