How do you examine the reticuloendothelial system? You have
certain procedures you perform for examining the other systems of the body. Most textbooks
list the 10 major organ systems of the body that maintain homeostasis, but few mention
specific examination procedures for the reticuloendothelial system.
That is because this very important system is not composed of visceral organs, but
rather macrophages that are found in connective tissue. They carry on the process of
phagocytosis or detoxification in critical areas of the body.
You will recall that 60% of body weight is water, and of that, two-thirds of this fluid
is found inside the cells. The remaining one-third of total body water is found outside
the cells and is referred to as the extracellular fluid (ECF).
It is only the ECF that is involved with maintenance of homeostasis, that critical
process controlled by the autonomic nervous system and endocrine system through the
direction of the hypothalamus. The ECF is composed of the fluid in the blood stream (20%)
and the fluid outside the blood stream (80%) in the connective tissues. It is the
macrophages in the fluid of connective tissues that comprises the reticuloendothelial
system, or the macrophage system as it is sometimes called.
Obviously, since we are dealing with cells outside the blood stream, we cannot examine
the blood to get definitive answers. Nor will urinalysis yield much useful information.
X-rays, MRIs and cat scans are useless. Tissue biopsies are good, but outside the scope of
practice for D.C.s. So, how do you examine this critical system, and why would you want
to?
Macrophages are defined as mononuclear phagocytes found in the tissues. These cells
arise from stem cells in the bone marrow. They develop into monocytes and circulate in the
blood for about 40 hours.
Monocytes, as you know, are non-granular white blood cells that function as phagocytes
in the blood. They are transformed into macrophages after leaving the blood stream and
moving into the connective tissues. It is here that they undergo a magical metamorphosis
increasing in size, phagocytic activity and lysosomal enzyme content.
The lysosomal sacs of these cells contain hydrolytic (digestive) enzymes that are
active in an acid pH. This is an incredibly important point if you are using enzymes to
enhance immune function. Pancreatic enzymes are not active in an acid pH environment, only
in the alkaline environments found in the blood and small intestine.
Macrophages are most frequently concentrated in the following areas:
*** Loose connective tissues, which are especially numerous in mucous membranes of the
digestive and respiratory tracts and in association with the lymphatics in the connective
tissue of the pleura and peritoneum;
*** Lining the alveoli (terminal air sacs) of the lungs;
*** Lining the blood sinuses of the liver (Kupfer cells) and bone marrow;
*** Lining the sinuses of lymph nodes and the spleen, and
*** Microglia of the central nervous system. Microglia are small, non-neural,
interstitial cells of mesodermal origin that form the supporting structure of the central
nervous system.
Once in the connective tissues, the macrophages become powerful scavengers, even more
powerful than neutrophils. They have the ability to engulf not only much larger particles
but also larger quantities than the neutrophils.
Macrophages are capable of ingesting four times as much material as neutrophils before
dying. They can even phagocytize whole red blood cells and malarial parasites, whereas --
neutrophils are not capable of phagocytizing particles much larger than bacteria. Also,
macrophages have much greater ability to phagocytize necrotic tissue.
Phagocytosis
When these cells come in contact with extraneous particulate matter, either in the
tissues or in the blood stream, the phenomenon of phagocytosis takes place extremely
rapidly, the particle passing through the cell membrane to the inside of the phagocyte
within a few hundredths of a second.
Obviously, the phagocytes must be selective, otherwise some of the structures of the
body itself would be ingested.
Without going into great detail, it should be sufficient to say that phagocytosis is
dependent upon certain selective procedures. For example, if the surface of a particle is
rough, the likelihood of phagocytosis is increased, whereas a smooth particle is very
resistant to phagocytosis.
Also, the body has a means of selectively combining foreign particles with globulin
molecules called opsonins. Opsonins allow adhesion of the phagocyte to the surface of the
particle, which promotes phagocytosis.
Once a foreign particle has been phagocytized, the cell immediately begins digesting
the particle. Macrophages have proteolytic enzymes especially geared for digesting
bacteria and other foreign protein matter, as well as large amounts of lipases which
digest the thick lipid membranes possessed by certain bacteria.
In my upcoming columns, the focus will be on the individual organs that are supported
by the reticuloendothelial system. I will discuss specific nutritional supplementation
protocols for the spleen and lymphatic system, liver, and mucous membranes of the
digestive and respiratory tracts.
(Dr. Loomis welcomes input on the subjects covered in this column. To ask a
question, or make a comment, call him at 800-662-2630. Or write: 6421 Enterprise Lane,
Madison, WI 53719.)