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Untitled - D Ank Unlimited

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thymus 699 thymus<br />

Marrow<br />

stem cell<br />

TdT –<br />

Lyt –<br />

θ –<br />

β 3<br />

FR.5<br />

Prothymocyte FR.5 Thymocyte<br />

TdT +<br />

Lyt –<br />

θ, + θ –<br />

Bone marrow Thymus<br />

The normal thymus of infant showing lobulation and sharp separation of<br />

cortex from the stalk-like medulla (40× magnification).<br />

markers for thymic tissue. The blood supply to the cortex<br />

comes from capillaries that form anastomosing arcades.<br />

Drainage is mainly through veins; the thymus has no<br />

lymphatic vessels. The thymus develops from the branchial<br />

pouches of the pharynx at about 6 weeks of embryonal age.<br />

β 4<br />

α 1<br />

α 7<br />

Thymosin<br />

TdT +<br />

Lyt 1 + 2 + 3 +<br />

θ ++<br />

FR.5<br />

α 1<br />

Peripheral<br />

lymphoid tissue<br />

Proposed site of action of thymosin polypeptides on maturation of T cell subpopulations.<br />

Normal adult thymus. The thymus often shows an X- or H-shaped<br />

configuration.<br />

α 7<br />

?<br />

Hassall’s corpuscle.<br />

T-cells<br />

suppressor<br />

Killer<br />

Helper<br />

TdT –<br />

Lyt 1 + 2 + 3 +<br />

θ +<br />

Hassall’s<br />

corpuscle<br />

In most species, it is fully developed at birth. In humans,<br />

the weight of the thymus at birth is 10 to 15 g. It continues<br />

to increase in size, reaching a maximum (30 to 40 g) at<br />

puberty. It then begins to involute with increasing age, but<br />

remains functional. The medulla involutes first with pyknosis<br />

and beading of the nuclei of small lymphocytes, giving<br />

a false impression of an increased number of Hassall’s<br />

corpuscles. The cortex atrophies progressively. The blood–<br />

thymus barrier protects thymocytes from contact with<br />

antigen. Lymphocytes reaching the thymus are prevented<br />

from contact with antigen by a physical barrier. The first<br />

level is represented by capillary walls with endothelial cells<br />

inside the pericytes outside the lumen. Potential antigenic<br />

molecules that escape the first level of control are taken<br />

over by macrophages present in the pericapillary space.<br />

Further protection is provided by a third level, represented<br />

by a mesh of interconnecting epithelial cells that enclose the<br />

thymocyte population. The effects of thymus and thymic<br />

hormones on the differentiation of T cells are demonstrable<br />

in animals congenitally lacking a thymus (nu/nu animals),<br />

in neonatally or adult thymectomized animals, and in<br />

T

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