WBC's and platelets

WBC

Types of granulocytes

neutrophil

eosinophils

basophils

band, seg

maturation stages

myeloblast

promyelocyte

myelocyte

metamyelocyte

band

seg

When reading a slide be on the conservative side and call it the more mature one

0-2% in bone marrow

15-20 μm, 7:1-5:1 nucleus

no granules, basophilic cytoplasm

1-3 nucleoli

no clumping chromatin

1-4% in bone marrow

12-24 μm, 5:1-3:1 nucleus

little clumping

azurophilic granules in basophilic cytoplasm

1-2 nucleoli

5-20% in the bone marrow

10-18 μm, 2:1- 1:1 nucleus

slight clumping (way to differentiate from promyelocyte)

blueish pink cytoplasm, azurophilic granuoles

0-1 nucleoli ( most likely wont see it

5-15% in the bone marrow

10-18 μm, 1:1 nucleus (big identifier to differentiate from myeolocyte

basophilic chromatin

pink with granules cytoplasm

0 nucleoli

10-35% in the bone marrow

10-16μm, 1:1-1:2 nucleus

pink, violet pink granuoles cytoplasm

clumped chromatin

0 nucleoli

smooth indented nucleus

10-16μm, 1:3 nucleus

5-15% in the bone marrow

pink, violet pink granuoles in cytoplasm

clumped chromatin

multiple lobes connected

0 nucleoli

very clumped blue-purple chromatin

0-1% in bone marrow

10-16μm

pink with red big granule in cytoplasm

bilobed nucleus

promyelocytes can be indentified cytochemically

10-16μm, 1:3 nucleus

0-1% in bone marrow (least amount)

pale blue with black-blue granules

very clumped chromatin

identified by purple granules

granules can be washes away in staining

neutrophil kinetics

movement between pools

Neutrophils split 50/50 in the periferal blood in the circulating pool or the marginal pool
there for 10 hour

bone marrow

mitotic pool

12-21 days

maturation and storage pool

6-7 days

vasculature

6-14 days

tissue

4-5 days

stop or slow foreign material

phagocytized of the foreign material

moving to area of inflamation

neutrophilia increase in WBC

bone marrow 3-6 days, vasuculature 8-18 hours

anti- inflamitory, defense against helminth parasites

7 hrs in bone marrow, 10 hours in vascular

hypersensitivity immune reactions

Monocytes: monoblast

15-25μm, 7:1-4:1 nucleus

fine chromatine

0-1% in bone marrow

1-2 nucleoli

moderately basophilic cytoplasm, no granules

promonocytes

monocyte

14-20μm, 4:1-2:1 nucleus

0-1% in bone marrow

reticular pattern for chromatin

paler blue-gray cytoplasm

0-2 nucleoli

0 nucleoli

reticular pattern chromatin

12-18μm, 1:1-2:1 nucleus

0-2% in bone marrow

pale blue gray cytoplasm, has red dust like particles

has vacuoles

macrophage

when monocytes are in tissues

can enlarge in size

kupffer (liver), splenocytes (spleen), dust lungs, Langerhans (skin)

bone marrow (55 hours)

vasculature 8-12 hours

months

phagocytosis, defense mechanism (microorganism and tumor cells), scavenger (damage cells, plasma proteins, plasma lipids), breaks down heme oxidase to get to iron, process antigens for lymphocyts, produce and secrete substances

platelets (thrombocyte)

thrombocytopenia- <150k of platelets

thrombocytosis >450k of platelets

pre megakaryoplast

megakaryoblast

bfu, cfu, ld-cfu meg cant be distinguished on the microscope

CFU, BFU goes through mitosis and LD-CFU goes through endomitosis

DNA doubles but it doesnt split

promegakaryocytes

red-purple fine chromatin

basophilic nongranular cytoplasm

1-2 nucleoli

20-45μm, 5:1-3:1 nucleus

megakaryocyte

increased red-purple fine chromatin

basophilic, azurophilic granules

0-1 nucleoli

20-80μm, 3:1-1:1 nucleus

Platelet

blue-purple granular chromatin

pale blue with pink hue, many azurophilic granules cytoplast

0 nucleoli

30-100μm

"mother cell"

no nucleus

light blue-purple cytoplasm

1-4μm

kicks out nucleus

bone marrow (5-7 days)

vasculature (7-10 days)

hemostasis through fibrin production, stop bleeding

lymphocytes

AG independent development: primary organs (bone marrow and thymus)

AC dependent development; secondary organs (spleen, lymph nodes, tonsils, etc)

T cell differenciates in thymus, b cell in bone marrow

pre-lymphoblast is indistiguishable from one another

lymphoblast

prolymphocyte

basophilic cytoplasm

1-2 nucleoli

no clumping chromatin

10-20μm, 7:1-4:1 nucleus

indistinguishable to a myloblast to the untrained eye

small lymphocyte

0-1 nucleoli

clumped, blue purple chromatin

basophilic cytoplasm

9-18μm, 5:1-3:1 nucleus

0 visible nucleoli

dark purple, clumped chromatin

basophilic cytoplasm

7-10μm 4:1-2:1 nucleus

medium lymphocyt

large lymphocytes

pale-blue, may contain azurophilic granules

10-12μm

chromatin is clumped, no nucleoli

clear, pale, may contain azurophilic granulescytoplasm

13-15μm

coarse chromatin

5% in peripheral, 95% in vascular

bone marrow- 3days, vasculature 3-4 days, can be up to 10 years

can move between whenever they want

Function

B- humoral immunity (antibodies)

t- cell mediated immunity

secretion of lymphokines

helper, cytotoxic, suppressor

atypical (reactive) lymphs: outside normal standards

if many may be battling viral infection

abnormalities in WBC

toxic granulation

heavy darkened granules in neutrophils

shows severe infections, drug poisoning, and burns

Dohle bodies

light blue area in cytoplasm of neutrophil

shows infections, poisoning, burns, chemo, toxemia of pregnancy, may-hegglin anomaly

hypersegs

6 or more lobes in a neutrophil

shows megaloblastic anemis, chronic infection, Undritz anomaly

vacuolated

result of phagocytosis

shows septicemia, severe infection, can be from storage in EDTA

degenerated

structureless mass (pyknotic nucleus)

not counted in differential

storage in EDTA

pelger- huet anomaly

bi-lobed nucleus (glasses)

benign inherited disorder, myelocytic leukemia, severe infection

Chediak- steinbrinck-higashi syndrome

red-purple granuoles in cytoplasm

rare fatal disorder

alder-reilly anomally

blue-black granulation throughout

hurlers or hunters syndrome (inherited)

may-hegglin anomaly

larger than normal dohle, giant platelets are also here

inherited disorder

auer rods

red-purple rods in myeloblasts, mono, promyelocytes

showed in acute monocytic leukemia, acute mylogenous leukemias erythroleukemia

smudge cells

disintegrating nucleus

increased chronic lymphocytic leukemia, rupture during cell prep

platelet satellitosis

reacting to serum factor of EDTA

platelets encircling neutrophils

average # platlets in 10 fields * 20000=confirmation on platelet count