1.1 Cell Adaptations

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    1.1 Cell Adaptations

    Types of Body Tissues

    1. Labile tissues

    Cells of these tissues undergo continuous

    turnover, where the mature cells are lost

    and replenished by maturation of stem

    cells or proliferation of other mature

    cells.

    Examples of such tissues include the

    bone marrow and epithelial surfaces

    (GIT, renal tubules, skin, mucous

    surfaces, lining of glands, etc.)

    2. Stable tissues

    Cells of these tissues are quiescent (i.e.

    have limited proliferative activity). When

    there is a growth stimulus (e.g. injury tothe tissue), however, they have the ability

    to proliferate.

    These tissues include the liver (e.g. when

    part of it is resected), endothelial cells,

    fibroblasts, and smooth muscle cells (thelatter three important in wound healing.)

    3. Permanent tissues

    Mature cells of these tissues cannot

    proliferate and there are no sufficientstem cells to replenish dead cells.

    Examples are striated muscle cells and

    neurons. If these tissues are injured, they

    will heal by scarring.

    Cell Adaptations

    When a cell encounters a new type of

    stress or demand, it will try to readjust

    itself in order to adapt to that stress while

    also maintaining its normal function. This

    process will work as long as the stress can

    be endured by the cell. The changes

    which a cell can undergo when there is

    stress are called adaptation and they are

    of four types:

    1. Hypertrophy2. Hyperplasia3. Atrophy4. Metaplasia

    1. Hypertrophy

    Hypertrophy is the increase in the size of

    cells of an organ leading to an increase in

    the size of the organ itself. The cells

    increase in size by increasing their

    structural proteins and their organelles.

    The stimulus for cells to undergo

    hypertrophy can be considered

    physiological (as in the case of increase in

    muscle cell size in weight-lifters) or

    pathological (as in the case of increase in

    cardiac muscle cell size in hypertension

    or when there is valve stenosis).

    If the stress persists , hypertrophy may

    not be able to keep compensating for it.

    Taking the heart as an example, if the

    hypertension persists (and worsens), the

    myocardium will start undergoing

    degenerative changes causing ventricular

    dilation. This can be explained by

    different causes such as:

    inability of blood vessels tosupply the demands of this

    enlarging heart

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    inability of mitochondria toprovide adequate ATP

    no more increase in myofilamentsThus, long-term stress can cause a switch

    from adaptation to actual cell injury.

    2. Hyperplasia

    Hyperplasia is an increase in the number

    of cells of a tissue. This process can be

    considered normal as in the case of:

    1. proliferation of the duct system inthe female breast at puberty

    2. regeneration of liver tissue after apart of it is resected

    Hyperplasia can be considered abnormal

    in cases like:

    1. endometrial hyperplasia due toexcessive stimulation by estrogen

    (when there is no enough

    progesterone to oppose it)

    2. skin warts caused by humanpapillomavirus (which allows the

    cells to go through the cell cycle,

    thus divide)

    Hyperplasia thus needs a stimulus tokeep going. If the stimulus is removed,

    hyperplasia will stop. This is the main

    difference between hyperplasia and a

    benign tumor (which doesnt need a

    stimulus to keep growing).

    3. Atrophy

    Atrophy is a decrease in the size of a cell.

    This is done in an effort by the cell to

    cope with situations like inadequate

    blood supply, undernutrition, disuse (in

    fractures for example), denervation

    (because this leads to disuse), loss of

    hormonal stimulation , or aging (senile

    atophy).

    This decrease in the size of the cell at the

    molecular level is due to a decrease in

    protein synthesis (because metabolism is

    slowed down) and an increase in protein

    degradation.

    How to destroy a protein (do not try this

    at home):

    1. Activate ubiquitin ligases bydecreasing your nutrition or by

    disuse of a tissue

    2. Allow ubiquitin ligases to gocleave and activate ubiquitin

    monomers

    3. Tag the protein you want todestroy with ubiquitins (so it is

    poly-ubiquitinated)

    4. Allow the hungry proteasome torecognize the ubiquitinated

    protein and break it down topieces (i.e. amino acids) in its core

    4. Metaplasia

    Metaplasia refers to the replacement ofmature epithelial cells by another type of

    mature epithelial cells.

    Normally the respiratory epithelium is

    composed of ciliated cells. Because

    tobacco smoke contains a lot of injuriousagents, the ciliated cells cannot easily

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    tolerate this stress so they will be

    replaced by stratified squamous cells

    which are more resistant to stress.

    This transformation occurs by

    reprogramming the genes of the local

    stem cells, which then divide and mature

    into squamous cells to take the place of

    the ciliated cells.

    While better resistance is achieved with

    squamous cells in this case, the squamous

    cells cannot secrete mucin nor do they

    have cilia to propel materials out of the

    respiratory tract. Thus there is loss of

    important function.

    Another example is in gastroesophageal

    reflux disease (GERD). When there is

    persistent or excessive irritation of the

    lower esophagus by acid reflux from the

    stomach, the normal squamous lining of

    the esophagus will be replaced by

    intestinal columnar cells which can resist

    the acid better. This in the long-term can

    cause adenocarcinoma of the lower

    esophagus.

    Metaplasia can also occur in

    mesenchymal tissues (like bone forming

    at site of injury) but are less common and

    are considered to be less important as an

    adaptive response.