|
Logical Biology 6 (3): 62-64,
2006 |
PERSPECTIVE |
|
http://logibio.com |
|
|
© Truthfinding Cyberpress (http://im1.biz/tfcp) |
CELL REPRODUCTION |
Cell
Division versus Cell Reproduction:
No
Evidence for Cell “Division”
Shi V. Liu
Eagle Institute of Molecular Medicine
(Part 1 received 2006-08-15; accepted 2006-08-25;
Part 2 received 2006-09-15, accepted 2006-0929;
Both
published 2006-09-30*)
HIGHLIGHT
A serious discussion on the problems
and pitfalls of describing cell reproduction as a cell “division” was made. However, “top” scientific journals rejected
to publish this discussion even in its short format.
ABSTRACT
Symmetric “cell division” has
been a rooting concept for microbiology and cell biology that has contributed
to a distorted view on microbial/cell life for centuries. A proposal is made here to replace “cell division”
with “cell reproduction” to better capture the reality and to help unifying
biology. This change in terminology should
not be treated as a simple wording game but a fundamental revolution in
microbiology/cell biology.
KEY WORDS
Cell reproduction, Cell “Division”,
Cell age, Cell life, Cell death, Cell “cycle”, Cell Reproduction cycle
Part 1. Cell Division versus Cell
Reproduction
“Cell division” is a very common term used in
scientific researches and publications.
The term might have taken its root from the early microscopic
observations on some so-called “symmetric” microbes which form two “identical”
cells from the previous one cell. To the
early microbiologists/cell biologists, there was indeed no way to argue for any
distinction between the two cells formed from the one cell. Thus, microbiologists or cell biologists have
simply called these two cells formed from one cell as identical daughter
cells. However, by doing so,
microbiologists/cell biologists in fact have violated a basic life principle:
reproduction means succession of generation which means there is a genuine
chronological age difference between the old template and the new copy.
Perhaps microbiologists/cell
biologists have realized the dichotomy they created for biology. Thus, instead of calling it as “cell
reproduction” to conform to the normal scientific rule and logical pattern of
classifying sub-level term/concept under its higher level term/concept, they
used a new term “cell division” or “cell fission”. By definition, division or fission does not
intrinsically entail any mechanism of reproduction and thus it theoretically
does not have a need to abide by any life principle related with reproduction.
Thus, ever since the
beginning of microbiology/cell biology, the reproduction processes of
microbes/cells have been described as some automatic cycling processes. “Cell cycle” has even become a standard term
for cell reproduction cycle. Even though
the subject under study is really a reproduction process, many cell biologists
(including microbiologists) have never taken any serious consideration over the
very fact that the objects they are studying in the reproduction process should
contain an old template and a new copy. Some
microbiologists/cell biologists even became very upset when such possibility
was pointed out. In the words of one
such expert “The semantic metaphors of “mothers and babies” and “life cycles
and immortality” may be of interest to philosophers but are not of any
practical or theoretical value that I can see.” (Logical Biol. 5: 254-271, 2005).
An expert on “cell division cycle” even claimed that my alternative view
on microbial/cell life (Sci. China
42: 644-654, 1999; Logical Biol. 1:
5-16 and 25-31, 2000; 4: 1-6, 7-15, 16-27 and 88-101, 2004; US patent 6767734B,
2004; Trends Biotechnol. 23:9-10,
2005) will cause “confusion as to the nature and study of the cell cycle” when
he wrote in a Commentary that was initially accepted for publication by Trends in Biotechnology but later
withdrawn from publication by that journal after the editor and board members
read my reply to this Commentary (my reply was later published in Logical Biol. 5: 335-349, 2005 but that
expert has refused repeated invitations to publish his Commentary in Logical Biol.)
However, increasing evidence
has now shown that the so-called “symmetric” cell division is not “typical” at
all and could not even serve as a representative for the diversified manners of
cell reproduction. Many so-called
“asymmetric” cells/microbes actually “divide” asymmetrically. More importantly, at the molecular level,
even the so-called “symmetric” cells/microbes are not symmetric in their bodies
and in their “divisions”. Unfortunately,
facing such an overwhelming amount of “inconsistent” data that contradict the
dogmatic view of cell and cell division, microbiologists/cell biologists are
not willing to reconsider the validity of their long-inherited “symmetry”
assumption on cell body and the “equality” principle in cell division. Mainstream microbiologists/cell biologists
are still closing their door tight to alternative views which in fact have
provided much clearer insight to the underlying mechanisms of cell reproduction
and cell aging (Logical Biol.
Furthermore, instead of
correcting the fundamental mistakes in understanding cell reproduction, some
microbiologists/cell biologists have come up with additional extreme
claims. They called the two different
cells formed from one cell as either non-identical daughters or daughters with different
fates. To them, the difference between
the two cells is not a reflection of the generation/age difference as a result
of a normal reproduction but a result of the so-called “cell
differentiation”. Believe it or not, some
microbiologists have even claimed that this “cell differentiation” has occurred
even in some unicellular microbes (Logical
Biol.
However, my over twenty-years’
search on the evidence for the “one mother two daughter” “cell division”
concept has ended with an empty hand. To
the contrary, I have found more recordings in literature (Logical Biol. 5: 350-355, 2005; PloS
Biol. 3: 295-300, 2005) that actually accommodate my view of the
microbial/cell life. In my view, whether
a cell/microbe has a symmetric or an asymmetric body, its reproduction is
always asymmetric in the sense that one cell still retains the old templates and
existing materials (being it a strand of original DNA or else) and the other
cell must form such molecules/structures (at least with some new materials). Thus, the differences in age between two
cells formed from one cell are not limited to the cell level as one should be
called as the mother the other as the daughter but are present at the deep
underlying levels.
Thus, for the correctness of
reflecting a reality and the consistence of organizing scientific knowledge, I
appeal to use “cell reproduction” instead of “cell division” and “cell
reproduction cycle” instead of “cell division cycle”. I strongly denounce the short form “cell
cycle” because it is even more problematic than the long form “cell division
cycle”. This ambiguous term may create
an illusion that cells (as living individuals) are actually being cycled. In fact, this situation has been reflected in
the “immortality” view on cells when the “cell cycling” is considered as
something that will continue indefinitely unless external environment does not
provide supporting living conditions.
I should point out that the
proposed terminology change is not simply a naming game. No matter how trivial this change appears in
the surface of words it indeed has far-reaching implications. For example, it not only paves a way for
unifying biology under truly common life principles but also provides some
conceptual frameworks to understand cell-based biology. For instance, the popular proposal of the so-called
“immortal strand DNA” hypothesis for stem cell may just be a misunderstanding
of the cell aging process and the so-called “self-renewal” property of stem
cells may simply a reflection that these cells may just stay alive longer than
the so-called one “cell cycle” or, as often the case, simply called the “life
cycle”.
Logically speaking, “cell
cycle” is not an equivalent term for “life cycle”. Just as we should not simplify human life
cycle into human cycle, we should not simplify cell (as an individual not a
process) as “cell cycle”. However, we
can perfectly say reproduction cycle as a way to describe the common process
repeated in many different individuals or even species.
I must confess that I am not
optimistic with the even a slow acceptance of my proposed terminology
change. “Cell cycle” has become such a
popular “sound-bite” that any alternative saying would be heard as awkward if
not awful. To eradicate its strong impact
that has been buried deeply in people’s minds some thorough brain washes are
necessary. Fortunately some washing
solutions are already shelved in Logical
Biology (http://logibio.com) and more are
coming from different parts of the world.
Part 2. No Evidence for Cell “Division”
Cell “division” represents a fundamental concept and even
a cardinal principle in cell biology and microbiology (Cell 100: 71-78, 2000). By
choosing the word “division” cell biologists/microbiologists have satisfied
their need for explaining why two “identical” or “similar” cells can be “found”
(perceived) as a result of the “growth” of one cell and avoided a criticism for
their artificial creation of a dichotomous biology where microorganisms/cells
do not follow the basic life principle – reproduction means generation of a
chronologically young body from a chronologically old body.
However, careful literature
examination (Logical Biol. 1: 5-16
and 32-49, 2000; US patent 6767734B, 2004) has not yet revealed a single piece
of evidence that demonstrates cell “division” – dividing existing cell structure and content. Early observations on cell “division” have
emphasized its “symmetric” nature.
However, more and more later studies have showed that not only many
cells’ “divisions” are morphologically asymmetric but also many “symmetrically
divided” cells are unequal in their cellular contents or behaviors (Sci. China 42: 644-654, 1999; Logical Biol. 4: 7-15, 16-27, 2004). Unfortunately, these asymmetric observations
have not been truly understood by mainstream cell
biologists/microbiologists. Sometimes,
these differences were just simply attributed to the so-called “cell
differentiation”. Believe it or not, “cell
differentiation” has even been claimed for unicellular microbes (Logical Biol.
It turned out that cell
biologists/microbiologists’ mistake in falsely characterizing cell reproduction as cell “division” was not
only due to some deficiencies in experimental observations in the early studies
but also some fallacies in logical reasoning (Logical Biol. 1: 17-20 and 25-31, 2000). This conceptual mistake in fact has installed
a much stronger constraint on the thinking of cell biologists/microbiologists
that prevented them from objectively and correctly interpreting any new
findings that are contradictory to their established dogma (Trends Biotechnol. 23:9-10, 2005; Microbe 1: 1, 2006).
However, with enough
experimental evidence (Sci. China 42:
644-654, 1999; Logical Biol. 4: 7-15
and 16-27 2004; 5: 350-355, 2005) to light up the center stage of cell research
– cell reproduction mechanisms and implications – and, more importantly, with the
existence of a new alternative cell life theory (Sci. China 42: 644-654, 1999; Logical
Biol. 5: 51-55 and 109-116, 2005), it is time to move across the cell
“division” barrier in understanding cell biology/microbiology. Let’s say the process of forming two cells
from one cell is a reproduction
process and the two cells so-formed are not of any twin daughter relationship
but a true parent-child relationship!
So I appeal cell
biologists/microbiologists to use the more truthful and universal terms “cell
reproduction” and “cell reproduction cycle” and get ride of the untruthful and idiosyncratic
terms “cell division” and “cell division cycle”. I believe that this terminology change and,
more importantly, this conceptual brain wash will benefit cell
biologists/microbiologists for long run in their future efforts of
understanding the true life of cells/microorganisms.
* This publication
contains two parts which address the same issue but were written for different submission
purposes. The longer version (first part
here) was first submitted to Cell on 2006-08-15
and was rejected on 2006-08-17. Then it was submitted to Science on 2006-08-21 but was rejected 2006-08-25. A much shorter version (second part here) was
submitted to Science on 2006-09-15
but again was rejected on 2006-09-29. The publication here contains the original
content as submitted to Science
except with added highlight and keywords.