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Understanding Blood as Connective Tissue

Blood is classified as a liquid connective tissue composed of plasma and formed elements. Plasma is 91.5% water and contains proteins. Formed elements include red blood cells, white blood cells, and platelets. Red blood cells contain hemoglobin and transport oxygen. White blood cells help fight infection in two categories - granulocytes which have granules, and agranulocytes which do not. Platelets help form blood clots to stop bleeding from damaged blood vessels. The bone marrow produces all blood cells through hematopoiesis regulated by hormones like erythropoietin. Hemostasis stops blood flow through platelet plug formation, vascular spasms, and coagulation into a clot.
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0% found this document useful (0 votes)
13 views8 pages

Understanding Blood as Connective Tissue

Blood is classified as a liquid connective tissue composed of plasma and formed elements. Plasma is 91.5% water and contains proteins. Formed elements include red blood cells, white blood cells, and platelets. Red blood cells contain hemoglobin and transport oxygen. White blood cells help fight infection in two categories - granulocytes which have granules, and agranulocytes which do not. Platelets help form blood clots to stop bleeding from damaged blood vessels. The bone marrow produces all blood cells through hematopoiesis regulated by hormones like erythropoietin. Hemostasis stops blood flow through platelet plug formation, vascular spasms, and coagulation into a clot.
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Download as DOCX, PDF, TXT or read online on Scribd

BLOOD

“classified as a liquid connective tissue”

FUNCTIONS OF BLOOD BLOOD PLASMA

● Protection ● Composed of approximately


● Transportation 91.5 percent water, 8.5 percent
● Regulation solute most of which are
protein (7% by weight)
PHYSICAL CHARACTERISTICS OF
BLOOD

● Color range
● Oxygen-rich blood is scarlet
red
● Oxygen-poor blood is dull
red
● pH must remain between
7.35–7.45
● Blood temperature is slightly
higher than body
temperature

COMPONENTS OF BLOOD

● Blood Plasma - a watery liquid


extracellular matrix that
contains dissolved FORMED ELEMENTS
substances
● Formed elements - are cells ● Red blood cells
and cell fragments. ● White blood cells
● Platelets

RED BLOOD CELLS


(ERYTHROCYTES)

● Contain the
oxygen-carrying
protein
hemoglobin which
is a pigment that
gives whole blood
its red color.
● RBCs are biconcave discs with a
diameter of 7-8 micrometer.
BLOOD
“classified as a liquid connective tissue”

● RBC are highly specialized for ● They stain red-orange with


their oxygen transport function. acidic dyes
● Lives only about 120 days ● The granules usually do not
because of the wear and tear cover or obscure the nucleus,
their plasma membranes which most often has two
undergo as they squeeze lobes connected by a thick
through blood capillaries. strand of chromatin.
● Found in response to
PRODUCTION OF RBC
allergies and parasitic worms
Erythropoiesis
BASOPHIL
● it is the production of RBCs
-The round, variable-sized granules
● starts in the red bone marrow
of a basophil are basophilic
with a precursor cell called a
proerythroblast ● they stain
● a cell near the end of the blue-purple
development sequence ejects with basic dyes
its nucleus and becomes a ● have
reticulocyte histamine- containing
granules
WHITE BLOOD CELLS
● initiate inflammation
(LEUKOCYTES)
NEUTROPHIL
● have nuclei and do not
contain hemoglobin. -The granules of a neutrophil are
● classified into granular and smaller, evenly distributed, and pale
agranular lilac in color

Granular – granules in their ● The nucleus has


cytoplasm can be stained two to five
lobes,
Agranular – Lack visible
connected by
cytoplasmic granules
very thin
GRANULAR LEUKOCYTES strands of chromatin.
EOSINOPHIL ● Act as phagocytes at active
sites of infection
● Has a large,
uniform sized AGRANULOCYTES MONOCYTES
granules
● -are 12–20 μ m in diameter
BLOOD
“classified as a liquid connective tissue”

The nucleus of a develop into precursor cells


monocyte is usually called megakaryoblasts
kidney shaped or ● Platelets help stop blood loss
horseshoe shaped, and from damaged blood vessels
the cytoplasm is blue by forming a platelet plug.
gray and has a foamy appearance. ● Their granules also contain
chemicals that, once released,
The color and appearance are due
promote blood clotting.
to very fine azurophilic granules,
Platelets have a short life
which are lysosomes.
span, normally just 5 to 9
● Largest of the white blood days.
cells
HEMATOPOEISIS
● Function as macrophages
● Important in fighting chronic ● Blood cell formation
infection ● Occurs in red bone marrow
● All blood cells are derived
LYMPHOCYTES
from a common stem cell
The nucleus is round (hemocytoblast)
or slightly indented ● Hemocytoblast
and stains darkly. differentiation
o Lymphoid stem cell produces
The cytoplasm stains
lymphocytes
sky blue and forms a
o Myeloid stem cell produces
rim around the nucleus
other formed elements
The larger the cell, the more
CONTROL OF ERYTHROCYTE
cytoplasm is visible.
PRODUCTION
May be as small as 6–9 μ m in
● Rate is controlled by a
diameter or as large as 10–14 μ m in
hormone (erythropoietin)
diameter.
● Kidneys produce most
● Nucleus fills most of the cell erythropoietin as a response
● Play an important role in the to reduced oxygen levels in
immune response the blood
● Homeostasis is maintained by
PLATELETS
negative feedback from blood
● Myeloid stem cells develop oxygen levels
into mega karyocytecolony-
forming cells that in turn
BLOOD
“classified as a liquid connective tissue”

DEVELOPMENTAL ASPECTS OF
BLOOD

Sites of blood cell formation

● The fetal liver and spleen are


early sites of blood cell
formation
● Bone marrow takes over
hematopoiesis by the seventh VASCULAR SPASMS
month
● Fetal hemoglobin differs from ● Anchored platelets release
hemoglobin produced after serotonin
birth ● Serotonin causes blood vessel
● muscles to spasms
● Spasms narrow the blood
HEMOSTASIS vessel, decreasing blood loss
● Stoppage of blood flow COAGULATION
● Result of a break in a blood
vessel ● Injured tissues release
● Hemostasis involves three thromboplastin
phases ● PF3 (a phospholipid) interacts
o Platelet plug formation with thromboplastin, blood
o Vascular spasms protein clotting factors, and
o Coagulation calcium ions to trigger a
clotting cascade
PLATELET PLUG FORMATION ● Prothrombin activator
● Collagen fibers are exposed converts prothrombin to
by a break in a blood vessel thrombin (an enzyme)
● Platelets become “sticky” and ● Thrombin joins fibrinogen
cling to fibers proteins into hair-like fibrin
● Anchored platelets release ● Fibrin forms a meshwork (the
chemicals to attract more basis for a clot)
platelets BLOOD CLOTTING
● Platelets pile up to form a
platelet plug ● Blood usually clots within 3 to
6 minutes
● The clot remains as
endothelium regenerates
BLOOD
“classified as a liquid connective tissue”

● The clot is broken down after ● These antigens, called


tissue repair agglutinogens occur in
characteristic combinations.
UNDESIRABLE CLOTTING
Based on the presence or
Thrombus absence of various antigens,
blood is categorized into
● A clot in an unbroken blood
different blood groups.
vessel
● Within a given blood group,
● Can be deadly in areas like
there may be two or more
the heart
different blood types.
Embolus ● Large losses of blood have
serious consequences
● A thrombus that breaks away
o Loss of 15 to 30 percent
and floats freely in the
causes weakness
bloodstream
o Loss of over 30 percent
● Can later clog vessels in
causes shock, which is fatal
critical areas such as the brain
● Transfusions are the only way
BLEEDING DISORDER to replace blood quickly
● Transfused blood must be of
Thrombocytopenia
the same blood group
● Platelet deficiency
HUMAN BLOOD GROUPS
● Even normal movements can
cause bleeding from small ● Blood contains genetically
blood vessels that require determined proteins
platelets for clotting ● A foreign protein (antigen)
may be attacked by the
Hemophilia
immune system
● Hereditary bleeding disorder ● Blood is “typed” by using
● Normal clotting factors are antibodies that will cause
missing blood with certain proteins to
BLOOD GROUPS AND clump (agglutination)
TRANSFUSION ABO BLOOD GROUPS
● The surfaces of erythrocytes Based on the presence or absence of
contain a genetically two antigens
determined assortment of
● Type A
antigens composed of
● Type B
glycoproteins and glycolipids.
BLOOD
“classified as a liquid connective tissue”

The lack of these antigens is called ● The first pregnancy usually


proceeds without problems
● Type O
● The immune system is
The presence of both A and B is sensitized after the first
called type AB pregnancy
● In a second pregnancy, the
The presence of either A or B is
mother’s immune system
called types A and B, respectively
produces antibodies to attack
the Rh+ blood (hemolytic
disease of the newborn)

Rh BLOOD GROUP

● Named because of the


presence or absence of one of
eight Rh antigens
(agglutinogen D) BLOOD TYPING
● Most Americans are Rh+
● Problems can occur in mixing ● Blood samples are mixed with
Rh+ blood into a body with anti-A and anti-B serum
Rh– blood ● Coagulation or no
coagulation leads to
Rh DANGERS DURING determining blood type
PREGNANCY ● Typing for ABO and Rh
● Danger is only when the factors is done in the same
mother is Rh– and the father manner
is Rh+ , and the child inherits ● Cross matching – testing for
the Rh+ factor agglutination of donor RBCs
● The mismatch of an Rh– by the recipient’s serum, and
mother carrying an Rh+ baby vice versa TRANSFUSION
can cause problems for the Is the transfer of whole blood or
unborn child blood components into the
BLOOD
“classified as a liquid connective tissue”

bloodstream or directly into the red the recipient does not have
bone marrow. antibodies that will attack the
donor RBCs.
A transfusion is most often given to
alleviate anemia, to increase blood HOMEOSTATIC IMBALANCES
volume (for example, after a severe
-Anemia is a condition in which the
hemorrhage), or to improve
oxygen-carrying capacity of blood is
immunity.
reduced. All of the many types of
Agglutination - is an antigen– anemia are characterized by
antibody response in which RBCs reduced numbers of RBCs or a
become cross linked to one another. decreased amount of hemoglobin in
the blood.

● Inadequate absorption of
iron, excessive loss of iron,
increased iron requirement,
or insufficient intake of iron
causes iron deficiency anemia
● Inadequate intake of vitamin
B12 or folic acid causes
megaloblastic anemia
● Insufficient hemopoiesis
resulting from an inability of
TYPING AND CROSS MATCHING
the stomach to produce
BLOOD FOR TRANSFUSION
intrinsic factor, which is
● To avoid blood-type needed for absorption of
mismatches, medical vitamin B12 in the small
technologists type the intestine, causes pernicious
patient’s blood and then anemia.
either cross-match it to ● RBC plasma membranes
potential donor blood or rupture prematurely in
screen it for the presence of
antibodies.
● Blood typing use antisera
● Cross-match - the possible
donor RBCs are mixed with
the recipient’s serum. If
agglutination does not occur,
BLOOD
“classified as a liquid connective tissue”

● hemolytic anemia in red bone marrow interferes


● Deficient synthesis of with the production of red
hemoglobin occurs in blood cells, white blood cells,
● thalassemia and platelets.
● Destruction of red bone
marrow results in aplastic
anemia.

The RBCs of a person with sickle-


cell disease (SCD) contain Hb-S, an
abnormal kind of hemoglobin.
When Hb-S gives up oxygen to the
interstitial fluid, it forms long, stiff,
rodlike structures that bend the
erythrocyte into a sickle shape

LEUKEMIA

-Refers to a group of red bone


marrow cancers in which abnormal
white blood cells multiply
uncontrollably.

● The accumulation of the


cancerous white blood cells

Common questions

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Erythropoiesis is the process of red blood cell (RBC) production, initiated in the red bone marrow by precursor cells called proerythroblasts. The kidneys produce erythropoietin in response to decreased oxygen levels in the blood, stimulating erythropoiesis as a form of negative feedback to restore homeostasis . Once the development sequence nears completion, the cells eject their nuclei to become reticulocytes, which mature into RBCs . This process ensures that RBC levels increase when more oxygen transport is required, maintaining efficient delivery of oxygen throughout the body.

White blood cells (leukocytes) are crucial in the body's immune system, defending against infections and foreign invaders. They are classified into granulocytes and agranulocytes. Granulocytes include neutrophils, which act as phagocytes at infection sites, eosinophils responding to allergies and parasitic worms, and basophils initiating inflammation through histamine release . Agranulocytes include monocytes, which differentiate into macrophages to fight chronic infections, and lymphocytes, important for adaptive immunity, as they produce antibodies and destroy infected cells . This classification reflects their varied roles in immune defense, involving both innate and adaptive immune responses.

Thrombocytopenia, characterized by low platelet levels, significantly impacts blood clotting. It leads to excessive bleeding even with minor injuries, as platelets are essential in forming initial plugs at wound sites . Hemophilia is a hereditary disorder where specific clotting factors are missing, impairing the coagulation cascade and preventing proper clot formation . Both conditions increase bleeding risks, requiring careful management to prevent severe blood loss and associated complications. Patient health can be compromised, necessitating medical interventions such as blood transfusions or administration of clotting factors to protect against excessive hemorrhage.

Blood groups are determined by specific antigens on erythrocytes, such as the ABO and Rh factors, which can trigger immune responses if mismatched during transfusions . In transfusion, blood must match both the ABO and Rh types to prevent agglutination and immune reactions . During pregnancy, an Rh- mother with an Rh+ fetus may become sensitized, causing her immune system to attack Rh+ blood cells in subsequent pregnancies, potentially leading to hemolytic disease of the newborn . Thus, proper typing is crucial in both transfusion and pregnancy management to avoid complications.

While coagulation is crucial for hemostasis, it can also lead to undesirable clotting, forming thrombi or emboli. A thrombus is a clot within an unbroken blood vessel, potentially obstructing blood flow and, if occurring in critical areas like the heart, can be fatal . An embolus forms when a thrombus breaks free and travels through the bloodstream, potentially lodging in vital organs like the brain, causing life-threatening blockages such as strokes . These events underscore the importance of tightly regulated coagulation processes, where any imbalance may trigger significant health risks, emphasizing the need for treatments that safely manage clot formation.

Oxygen levels have a direct influence on erythropoiesis through the regulation of erythropoietin production. When oxygen levels are low, typically detected by the kidneys, erythropoietin production is stimulated to increase RBC production, thereby enhancing the blood’s oxygen-carrying capacity . This ensures that tissues receive adequate oxygen supply despite initial deficiencies. Conversely, normal or high oxygen levels reduce erythropoietin production, slowing erythropoiesis and preventing an excess of RBCs, thereby maintaining homeostasis in the body’s oxygen transport system.

Anemia is characterized by reduced RBCs or hemoglobin, affecting oxygen transport. Iron deficiency anemia results from iron depletion due to poor absorption, increased requirements, or loss, leading to fewer hemoglobins for RBCs . Megaloblastic anemia arises from inadequate intake of vitamin B12 or folic acid, causing enlarged, dysfunctional RBCs. Pernicious anemia is due to lack of intrinsic factor, hindering vitamin B12 absorption necessary for RBC production . Hemolytic anemia involves premature RBC destruction, while thalassemia stems from deficient hemoglobin synthesis . Each type impacts bodily functions differently, impairing oxygen distribution and causing symptoms like fatigue and weakness.

Hemostasis is the process of stopping blood flow due to vessel injury, involving three phases: platelet plug formation, vascular spasms, and coagulation. Initially, when blood vessels are damaged, collagen fibers become exposed, causing platelets to adhere and release chemicals to attract more platelets, forming a plug . Subsequently, vascular spasms occur as platelets release serotonin, causing blood vessel muscles to contract and reduce blood flow . Coagulation follows, where injured tissues release thromboplastin, triggering a cascade involving several clotting factors and calcium, ultimately converting fibrinogen to fibrin. The fibrin meshwork stabilizes the platelet plug, effectively preventing further blood loss . This sequence ensures the vessel is repaired efficiently while minimizing bleeding.

Blood is classified as a liquid connective tissue primarily due to its physical characteristics and functions. Its color ranges from scarlet red when oxygen-rich to dull red when oxygen-poor, reflecting its role in oxygen transport . The pH of blood is maintained between 7.35 and 7.45, and its temperature is slightly higher than body temperature, which facilitates various biochemical processes . Blood plasma, composed primarily of water and proteins, acts as a medium for nutrient and waste transportation. The formed elements, including red blood cells, white blood cells, and platelets, are crucial for carrying oxygen, defense against pathogens, and blood clotting, respectively .

Blood typing and cross-matching are critical processes ensuring safe blood transfusions. Blood typing identifies the ABO and Rh antigens present on donor and recipient erythrocytes through specific antisera. Cross-matching involves combining donor's RBCs with the recipient's serum to check for agglutination, indicating incompatible blood . This process prevents transfusing blood that might cause immune responses or agglutination in the recipient, which could otherwise lead to severe transfusion reactions or fatalities. Thus, careful blood typing and cross-matching ensure that only compatible blood is transfused, minimizing potential complications .

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