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The Circulatory System: Blood Elements, Clotting, and the ABO and Rh Blood Groups
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The Circulatory System: Blood Elements, Clotting, and the ABO and Rh Blood Groups
1. Which of the formed elements would increase after the donation of a pint of blood
and why?
Following a transfusion of a pint of blood, the formed elements that are more likely to
increase in number are erythrocytes (red blood cells or RBCs). The reason is that RBCs are the
most abundant created elements in blood [approximately 4-6 million per mm3 (μl) of blood].
This represents approximately 45 percent of the total blood content, while plasma accounts for
55 percent, and the rest 1 percent consists of leucocytes (white blood cells or WBCs) and
thrombocytes (platelets). RBCs are abundant because they perform the critical function of
transporting oxygen from the lungs to the rest of the body and carbon dioxide from these other
parts of the body back to the lungs for exhalation (Marieb & Smith, 2016).
Blood coagulation or clotting is purposely intended to reduce excessive blood loss when
blood vessels rupture. Interaction of several plasma elements (procoagulants or clotting factors)
and others ingredients produced by injured tissues and platelets is required for this process to
proceed effectively (Periayah, Halim, & Saad, 2016). The process of clotting takes place in the
following three steps. In the first phase, the damaged platelets and tissues release platelet factor
(PF) 3 and tissue factor (TF), respectively. These elements activate the clotting cascade or
mechanism. In the second phase, PF3 and TF interact with other calcium ion and other clotting
factors, and in the process forming prothrombin factor – which transforms plasma prothrombin
into thrombin. The last step is the enzymatic polymerization of plasma fibrinogen proteins by
thrombin into an insoluble material known as fibrin. The fibrin is responsible for forming the
mesh-like strands that trap RBCs. This lays the groundwork for clots (Marieb & Smith, 2016).
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Blood typing refers to the process of classifying blood depending on the specific
glycoproteins present on the external surfaces (plasma membrane) of red blood cells. These
proteins are usually known as agglutinogens or antigens, and are determined genetically.
Typically, blood types are classified based on the presence of antigens A, B, or both and the
presence of the rhesus factor. In the ABO blood types, the agglutinogens (antigens) occur
together with plasma proteins known as agglutinins or antibodies. Today, several blood typing
methods exist, depending on many potential antigens, but the elements commonly typed for
include the antigens for Rh blood groups and ABO blood groups. There are four types of ABO
blood groups: A, B, AB, and O. People with blood group A carry the "A" antigen on their RBC
plasma membranes, whereas their plasma contains Anti-B. In the U.S., it is estimated that nearly
40 percent of whites, 27 percent of Blacks, and 28 percent of Asians have blood type A. On the
other hand, people with blood type B carry the "B" antigen while their plasma contain Anti-A
antibodies. Estimates suggests that 11 percent of Whites, 20 percent of Blacks, and 27 percent of
Asians in the U.S. are blood group B. The AB blood group individuals have antigens A and B
but no antibodies. This makes them universal recipients. Approximately 4 percent of Whites, 4
percent of Blacks, and 5 percent of Asians are blood group AB. Finally, blood group 'O' people
lack antigens on their RBC membranes but carry anti-B and Anti-A proteins in their plasma.
These individuals are universal donors. Roughly 45 percent of White, 49 percent of Black, and
For the Rh blood types, people whose RBCs contain the Rh antigen are described as
being Rh-positive (roughly 85 percent of people in the United States), while those without the Rh
antigen are Rh-negative. Contrary to ABO blood types, neither Rhesus negative or Rhesus
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positive people carry preformed anti-Rhesus agglutinins (antibodies). However, people who are
Rhesus negative can develop these antibodies when transfused for the first time with Rhesus
positive blood. These antibodies can react with Rhesus antigen when such people receive Rh-
positive blood in the future. This would result in clumping or agglutination and eventually cell
hemolysis.
As mentioned above, blood types are classified based on the presence of antigens A, B, or
both and the presence of the rhesus factor. In the ABO blood types, the agglutinogens (antigens)
occur together with plasma proteins known as agglutinins or antibodies. Typically, these plasma
proteins react with antigens absent on the individual's "own" red blood cells. It means that if the
blood group does not fit with that of the recipient, the antibodies in the recipient's plasma are
more likely to react with the antigens on the surface of the RBCs. This results in a process
known as agglutination or clumping and subsequently hemolysis. This is the primary reason why
blood typing is necessary before any transfusion is performed. For example, agglutination and
hemolysis is likely to occur when a recipient who is blood group A gets transfused blood type B.
In this case, the clumping occurs because the recipient is carrying Anti-B antibodies in his/her
plasma, which automatically reacts with antigen B found on the plasma membrane of the donor
However, there is no agglutination when blood group O is transfused to all other blood
types because there are no antigens in the RBC cell membranes in these blood groups. Blood
group individuals are often known as universal donors. On the other hand, no clumping occurs
when other types of blood are donated to AB blood group recipients because they lack
antibodies. These individuals are known as universal recipients. Finally, the same antibody-
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antigen interaction is expressed in rhesus blood groups. However, as mentioned above, both Rh-
negative and Rh-positive people do not have preformed antibodies. Rh-negative people are the
ones that can only develop anti-Rh antibodies once exposed to Rh-positive blood, and they
would react to subsequent exposures to Rh-positive blood, causing clumping and hemolysis
(Alhabbab, 2018).
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References
Marieb, E. N., & Smith, L. A. (2016). Human anatomy & physiology laboratory manual (12th
ed.). Pearson.
Periayah, M. H., Halim, A. S., & Saad, A. Z. (2016). Mechanism action of platelets and crucial