Fibers
•Collagen/ white fibers
•Elastic/yellow fibers
•Reticular fibers/Argyrophilic – fine collagen
fibers
COLLAGEN FIBRES
•In bundles branch,1-12um in dia, White
•H &E and Van Gieson:pink;masson’s
T:blue;
•Tensile force,birefringence,swell with
weak alkali,boiling convert it into gelatin.
•Synthesis:fibroblast,regulation,degradation
(MMP)
•Made of tropocollagen mol;made of 3
polypeptide chains(procollagen)
SYNTHESIS
•AA taken up by cells& linked PROα
CHAINS αchain 3chains join to form
PROCOLLAGEN MOL such mol leave
cell through secretory vacuoles to form
TROPOCOLLAGEN MOL aggregate to
form COLLAGEN FIBRILS.(vit C,oxy)
•Fibrillogenesis
TYPES
TYPE LOCATION
I(250nm dia) SKIN,BONE,TENDON,FASCIA,
CAPSULE
II(20 to 100nm) HYALINE CARTILAGE
,NOTOCHORD,INTERVERTEBRAL
DISC
III RETICULAR FIBRES,FETAL
SKIN,BLOOD VESSEL.
IV BASAL LAMINA,KIDNEY
GLOMERULI
RETICULAR
FIBRES(Argyrophilic)
•Collagen type III,Striation(68ηm),20ηm
diameter,do not bundle,uneven in
thickness.
•Form network by branching
•Silver impregnation:black but type I:brown
•H&E:not identified;
•More carbohydrates:PAS
•Early mechanicalstrenth,delicate,suporting
stroma in lymphatic T.(not thymus)
•Synthesis:reticular cells
RETICULAR FIBRES
ELASTIC FIBRES
•Run singly,branches,0.1-0.2μm in dia
•Not well stained H&E;Certain fixative
make them refractile then can be
visualised
•Composed of:central core of elastin &
surrounding network of fibrillin microfibril
•Lacks hydroxylysine,random distribution of
glysine:HYDROPHOBIC & random coiling.
•Vertebral ligaments,larynx,elastic A
WEIGERT’S STAIN
GROUND SUBSTANCE
•Glycoprotiens:keratan s
•Multiadhesive
glycoproteins:laminin,fibronectin
•Proteoglycans:aggrecan,decorin
Pr + long chain polysaccharide –
glycosoaminoglycans
(MPS)
» Sulphated
» Non sulphated
Ground Substance
•GSG linked with pr.
•Carry sulphate gr(so3-)Carboxyl gr(coo-).
•Thus proteoglycans r in long chain,
•Can retain water thus proteoglycans form
•semi-solid, gel:stiffness
•Molecular arrangement: sieve
•Barrier:kidney;gas exchange:lungs
GLYCOSAMINOGLYCANS
TISSUE CHOND
ROITIN
SULPHA
TE
DERMAT
AN
SULPHA
TE
HEPARA
N
SULPHA
TE
HEPARI
N
KERATA
N S.
HYALUR
NIC
ACID
TYPICAL
CT
+ +
CARTILA
GE
+ + +
BONE +
SKIN + +
+
+
BASEME
NT M
+
OTHERS B/V LUNGS MAST C CORNEA
INTER V
DISC
SYNOVI
AL
FLUID
HYALURONIC ACID
•Hyaluronan:free carbohydrate chain
•Polymers r very large
•Synthesized by enzymes ¬
posttranslatioally modified
•No sulfate,proteoglycan aggregates
•So cartilage resist compression without
inhibiting flexibility
CLASSFICATION OF C. T.
•Types of cells
•Types of fibres
•Amount of ground subs
CLASSIFICATION
CONNECTIVE TISSUE
ADULT C. T. FETAL C. T.
ORDINARY SPECIALISED
BLOOD
CARTILAGE
BONE
LOOSE C. T. DENSE C.T.
WHITE YELLOWAREOLAR
ADIPOSE
RETICULAR
REGULAR IRREGULAR
TENDON
LIGAMENT
APONEUROSIS
S/C TISSUE
FETAL C.T:WARTON’JELLY
LOOSE AREOLAR T.
Loose Connective
•Areolar Tissue
–Gel like matrix
–Fibroblasts, mast cells
–Collagen, elastic and reticular fibers
–Functions to wrap and cushion organs
–Found in the lamina propria, around organs,
capillaries
Dense Connective
•Dense Regular
–Parallel collagen fibers
with a few fibroblasts
and a few elastin fibers
–Attach muscles to
bones
–Great tensile strength
in one direction
–Tendons and ligaments
DENCE REGULAR C.T.
TENDON
Dense Connective
•Dense irregular
–Collagen fibers with a few elastic fibers
haphazardly arranged
–Strong in many directions
–Dermis, joint capsules, submucosa of
digestive tract
DENCE IRREGULAR C.T.
ADIPOSE TISSUE
APPLIED
•SCURVY:Vit C DEFICIENCY
•OSEOGENESIS IMPERFECTA:Brittle
bone disease,blue sclera hearing
loss,TYPE I asso
•EHLERS-DANLOS :hypermobility of joints
of digit,TYPE III asso
•MARFAN’S S:FBN1,fibrillin gene