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THYMUS
Dr. Pradipta Ray Choudhury
MBBS, MD, PhD
Associate Professor of Anatomy, SMCH, Silchar
• Thymus is a primary lymphoid
organ & the site of maturation of T
lymphocytes.
• thymus is fully formed &
functional at birth (c.f. LN, spleen,
tonsil etc. are under-developed at
birth) continues to grow until
puberty then begins to involute
& replaced by fatty tissue.
Thymus
- It is a bi-lobed
structure in thorax.
- It has only efferent
lymphatic.
Child
STRUCTURE
A. Connective tissue framework
- Capsule
- septae/trabeculae
- cellular reticulum- formed by
epithelial reticular cells.
B. Parenchyma
1. Cortex
2. Medulla and Hassall’s corpuscle.
 Covered by a connective tissue
capsule.
From capsule many septa/
trabeculae extend to the interior.
 capsule and trabeculae contain
blood vessels, lymphatics and
nerves.
A. Connective tissue framework
• These septa
divide thymus
into many
incomplete
lobules.
• Each lobule has
an outer dark
stained cortex &
an inner light
stained medulla.
The
medulla of
adjacent
lobules are
continuous
• The supporting stroma of the
organ within the lobule is formed
by epithelial reticular cells.
• These are stellate cells & their
cytoplasmic processes come in
contact with the processes of
neighbouring cells thus forming
a cellular reticulum within the
thymus.
This reticulum is different from the
reticulum of other lymphoid
organs where it is formed by
reticular fibres.
• In between the
epithelioreticular
cells, developing
T lymphocytes
(Thymocytes)
are found.
Epithelioreticular cells/ Epitheliocytes:
• Form the structural framework of
thymus.
• 6 types are recognised: Type I to
type VI.
• Secrete hormones like Thymulin,
Thymopoietin, Thymosin etc.
necessary for T lymphocytes
differentiation.
The epithelioreticular cells envelop
the thymic blood capillaries to
form the blood- thymic barrier.
Blood–Thymic Barrier
• It protects developing T lymphocytes
in the thymus from exposure to
antigens present in blood (which may
influence the developing T lymphocytes)
It is formed by:
1. Endothelium with basal lamina
2. perivascular space containing
Macrophages
3. Type I Epithelio-reticular cells
Perivascular
connective
tissue with
macrophage
lined by
endothelium
Parenchyma:
Cortex
The cortex is darkly stained
because it is densely packed with
developing T-lymphocytes
(thymocytes).
- Also contain few macrophages
and epithelioreticular cells(type
I,II,III).
T lymphocytes
T-lymphocyte of thymus/Thymocyte:
T cell precursors (lymphoblasts)
arrive in thymus from bone marrow.
• thus the outer cortex contains
larger lymphocytes
divide to form smaller maturing
lymphocytes which then move into
deeper cortex & then the medulla.
ultimately the thymocytes
leave the thymus as
immunocompetent T
lymphocytes
are released in circulation
through blood vessels &
lymphatics.
Medulla and Hassall’s Corpuscle
Medulla is lightly stained because
the lymphocytes are less densely
packed.
- For this reason the epitheliocytes
(type IV, V & type VI) in the
medulla appear to be numerous.
MEDULLA
- The most characteristic feature
of the medulla is the presence of
thymic (Hassall’s) corpuscles.
- these are acidophillic (pink
stain) small rounded structures
- are made up of closely packed,
concentrically arranged
epithelio-reticular cells (type VI).
MEDULLA
WITH
CORPUSCLE
• Each corpuscle has a central
core formed by degenerating
epitheliocytes & macrophages.
• number of Hassall’s corpuscles
increases with increasing age.
• functional significance
of Hassall’s corpuscles is not
known.
FUNCTIONS of thymus:
• thymus receives stem cells from
bone marrow
mature T lymphocytes are formed
(involved in cell mediated
immunity).
• mature T lymphocytes are then
carried to the lymph node, spleen
and other lymphatic tissue.
in thymus
• Thus Thymus is considered as a
central lymphoid organ and is
essential till puberty.
• After puberty the other
lymphatic tissues of the body are
fully developed; hence thymus
gets atrophied.
• Removal of thymus in newborn
→ failure of seeding of other
lymphoid organs with
immunocompetent T cells →
deficiency in immunological
competence to fight against
invading pathogens → infection
→ death.
Applied importance:
1.DiGeorge's syndrome :
Congenital failure of the thymus
to develop.
2. Thymectomy is done in severe
autoimmune diseases.
The End
EDUCATION OF T LYMPHOCYTES
Thymus in children Thymus in adult
Mucosa-Associated Lymphoid Tissue
(MALT)
• Mucosa-associated lymphoid tissue
(MALT) is localized lymphocyte
aggregation in the mucosa of the
gastrointestinal, respiratory tracts.
• Types: Gut-associated lymphoid tissue
(GALT), Bronchus-associated lymphatic
tissue (BALT).
MALT In GIT – gut associated
lymphoid tissue(GALT):
- Aggregated nodules (Peyer’s
patches)
- Lymphoid nodules in vermiform
appendix
- tonsils: form Waldeyer’s lymphoid
ring at the entrance of pharynx
Tonsils:
• These are a number of collection
of lymphoid tissues at the junction
of the oral cavity and pharynx.
• they guard the entrance to the
pharynx.
• They produce immune response
against the airborne and ingested
antigens.
• Types: palatine, pharyngeal,
lingual, & tubal tonsils.
lingual tonsil: present on the dorsum
of posterior 1/3rd
of tongue.
pharyngeal tonsil: single mass
situated in the posterior wall of the
nasopharynx.
Tubal tonsil: around the pharyngeal
opening of auditory tube
• The largest of these are the right
and left palatine
tonsils, present on either side of
the oropharyngeal isthmus.
Palatine tonsil
• palatine tonsils
are paired
structures
• The outer
surface is covered
by a connective
tissue capsule.
• The superficial aspect of the
tonsils is covered by stratified
squamous nonkeratinized
epithelium.
• The epithelium dips into the
substance of tonsil in the form of
several tonsillar crypts (10 - 12 in
number)
• The parenchyma of the tonsil is
composed of numerous lymphoid
nodules, many of which display
germinal centres.
Tonsillitis: enlargement of tonsils
due to infection/allergy.
The End
EDUCATION OF T LYMPHOCYTES