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MASSACHUSETTS NURSE NEWSLETTER ::
October 2005
It’s not nice to fool mother nature
Environmental pollutants and the immune system
By David H. Sherr, Ph.D.
Department of Environmental Health
Boston University School of Public Health
In evolution, surprisingly
little is left to chance. Biologic systems, whether composed
of millions of liver cells working in concert
to detoxify the blood, or white blood cells attempting to defend
against foreign microbe invasion, are “designed” with
controls, regulators, checks and balances. The selective value
of such biologic oversight is the evolution of systems that, despite
their complexity, tend not to fail.
For example, all animal cells are equipped with dozens of proteins
that regulate how frequently a cell divides. Should some of the
regulatory machinery become defective, cells generally invoke
a genetically encoded suicide program.
It actually takes several events to impair both growth regulation
and activation of the cell death program, and in that rare instance,
a cancer is formed. Even so, most tumors go undetected because
they are eliminated quickly by the sentinel immune system.
It’s when the balance between growth and death is tipped
in the direction of growth, and the immune system is impaired that
bad things happen. Our laboratory studies show how several environmental
pollutants do exactly that.
Immune system protects health
The immune system is responsible for defending its host against
invading bacteria, viruses, fungi, and, as noted above, newly
formed cancers. Defense against bacteria and fungi is assumed
primarily
by a system of interacting white blood cells known as the B lymphocyte
arm of the immune system.
B lymphocytes mass produce proteins (antibodies) which bind to
and kill microbes. Each B cell is capable of producing antibody
of only one given specificity. The development of millions of
B lymphocytes expressing millions of specificities insures that
the
immune system has the potential to respond to millions of different
foreign insults.
The B cells must “learn” their specificities early
in their development, must grow enough to constitute the host with
a significant mass of B cells of every given specificity, and must
learn not to respond to self components. B cells that fail to learn
the difference between “self” and “foreign” components
are forced to activate the suicide program, sparing the host from
autoimmune disease. This education occurs continually in the bone
marrow, where all eight kinds of blood cells are produced.
The failure of immature B lymphocytes to learn these lessons
results either in an inadequate immune response to foreign microbes,
leaving
the host susceptible to infection, or to an inappropriate autoimmune
reaction to host tissue.
Unfortunately, just like babies and
young children, bone marrow B cells are more sensitive to environmental
pollutants then their more mature counterparts.
Pollutants disrupt immune system
Our laboratory has shown that two classes of common pollutants,
aromatic hydrocarbons and phthalates, disrupt B cell education.
Hydrocarbons are ubiquitous and are produced every time something
organic is burned - from fossil fuels in our cars and coal in
our power plants, to charcoal broiled steaks. Phthalates, which
leach
from hundreds of common products containing plasticizers (e.g.
medical tubing, plastic bags, cosmetics), can also be found throughout
our environment.
The effects of these chemicals on immature B lymphocytes are
dramatic. Hydrocarbons, many of which are carcinogenic, prematurely
induce
bone marrow B cells to initiate the cell death program. Notably,
the doses of hydrocarbons required to suppress B cell development
are significantly lower than those required to induce cancers.
Consequently, estimates of hydrocarbon exposure risks, which
generally involve cancer as an endpoint, may underestimate the
dangers of
pollutant exposure.
It has been demonstrated that phthalates similarly induce programmed
cell death. Indeed, the strength of the death signal delivered
by phthalate-like chemicals is the strongest suicide signal our
laboratory has ever seen. At low doses, phthalates spare B cells
from the death program but induce them to cease growth.
Research focus
A key goal in our laboratory is to define, on a molecular level,
how these chemicals invoke aberrant cellular responses. Both
hydrocarbons and phthalates are recognized by distinct cellular
protein receptors
that transmit signals to cell nuclei wherein reside genetic programs
for cell suicide and growth regulation. This begs the question
of what these receptors evolved to do in the first place; certainly
they haven’t evolved to recognize by-products of human industry.
We must conclude then that activation of these receptors by environmental
chemicals is an unwise practice, one that clearly was not part
of Mother Nature’s evolutionary plan.
And we all know that it’s not nice to fool Mother Nature.
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