HIPA: Connective Tissue Flashcards
Connective Tissue Structure
Few Cells, lots of ECM
Connective Tissue Functions
a. The most important function of the connective tissue is to provide structural support
for the body.
b. Connective tissues are used for storage of metabolites.
c. Connective tissues play an important role in defense and protection of the body by
mediating immune, inflammatory, and allergic responses.
d. Connective tissues are used to “repair” other tissues and organs through the formation of
the fibrous scar.
Fiber Types
Three main types of fibers are present in connective tissue, collagen fibers,
reticular fibers, and elastic fibers. These fibers are formed by several types of fibrillar
proteins. Collagen and reticular fibers are composed of different types of collagen, while
the elastic fibers are composed of elastin and fibrillin.
Collagen
Collagen is an extracellular fibrillar protein and is the most abundant protein in the
human body. Collagen fibers are the principal structural components of most
connective tissues. They are flexible and have a high tensile strength. Collagen is
produced principally by fibroblasts. There are more than 28 different types of
collagens present in our body.
collagen structure
a. Collagen molecule measures ~300 nm and consists of three polypeptide
chains that form a triple helix. The synthesis and formation of collagen will
be covered in Biochemistry course.
b. Collagen molecules are polymerized laterally and head-to-tail to form
collagen fibrils. Fibrils cannot be visualized in the light microscope, but
have a distinctive banding when viewed with an electron microscope. The
banding is due to the presence of small gaps between collagen molecules,
which absorb stain.
c. Collagen fibrils in several types of collagens are assembled into collagen or
reticular fibers, which can be visualized in a light microscope.
d. Collagen fibers can be assembled into larger structures called the collagen
bundles, formed only by type I collagen.
Collagen Hierarchy
Bundle, Fibers, Fibrils, Molecules
T1 Collagen
Type I collagen is the principal type of collagen. It is found in the dermis of
the skin, tendons, ligaments, fascia, bone, and most connective tissues
proper. Type I collagen forms fibrils that are assembled into fibers, which
can be assembled into larger bundles.
Type II
Type II collagen is found in cartilage. This type of collagen forms fibrils,
but not fibers. Fibrils cannot be visualized in a light microscope and this
gives the cartilage its glassy appearance.
T3 Collagen
forms banded fibrils that assemble into reticular fibers,
which form a supporting framework for the cells of various tissues and
organs, such as the loose connective tissue, walls of blood vessels, lymphoid
tissues, bone marrow, smooth muscle, nerves, lung, etc. Reticular fibers are
named so because of their arrangement into a meshwork, or a network
(=reticulum).
T4 Collagen
Type IV collagen does not form banded fibrils, but forms sheet-like
meshwork of beaded filaments found in the basal lamina.
Ehlers-Danlos syndrome (EDS)
It is a congenital disorder, which is caused
by the impaired extracellular modification of collagen, which results in the
formation of defective collagen fibers. There many different types of EDS,
which have different symptoms. Typically, patients present with skin hyper
elasticity, loose, unstable joints that are prompt to dislocation, low muscletone/muscle weakness, and various bone abnormalities including deformities of the spine, osteopenia (low bone density), and others.
Elastic Fibers function
respond to stretch and distention
elastic fiber arrangement
thinner fibers in a branching pattern to form a network
elastic fiber stain
eosin may/may not work, orcein for selective staining,
Elastin
hydrophobic domain, cross-linked covalent bonds, fibers or lamellar layers (bl. vessels)
Elastin Function
elasticity (coming back) of conn. tissue, elastin molecules coil back into original shape
Fibrillin
glycoprotein, thin microfibrils that surround elastic fibers and provide substrate for assembly.
Marfan’s Syndrome
CV, skeletal, and ocular defects- mitral valve prolapse, rupture of arteries, arachnodactyly
Mutation in Fibrillin Gene
Ground Substances Function
Fill in ECM
Ground Substances Components
glycosaminoglycans (GAGs), proteoglycans,
and multiadhesive glycoproteins
GAGs structure
most abundant, long-chain, unbranched, highly neg charged polysaccharides
GAGs and water
hydrophilic so form a gel
GAGs function
resist compression/deformation, diffusion of water sol. particles
Hyaluronic Acid
GAG, always present in ECM, long molecule w/ no sulfate, does not form proteoglycans
Common Types of GAGs (CNCT)
Chondroitin sulfate, dermatan sulfate, keratan sulfate, and heparan
sulfate are some of the more common types of GAGs found in the
connective tissue. These GAGs attach to proteins to form proteoglycans.
Proteoglycan Structure and Hyaluronic Acid Aggregates
GAGs covalently attached to core protein, form brush structure, attach non-covalently to hyaluronic acid to form giant aggregates (hyaluronic acid aggregates)
Hyaluronic Acid Aggregates
Account for Connective Tissue ability to resist compression without losing flexibility (Q)
Multi-adhesive Glycoproteins Function
cross links between collagen, ECM, and Cells (think hemidesmosomes, focal adhesions)
Fibronectin pt. 1
most abundant glycoprotein in cnet tissue
Fibronectin pt. 2
can assemble into thin fibers, dimer that has binding domains for ECM (1,2,3 collagen), GAGs, integrin, fibrin, etc.
Integrin is a big one
Laminin
Basal Lamina, binding to 4 collagen, integrin, etc.
Three disulfide linked polypeptides
Cell adhesion sites
Resident Cells Characteristics
(fixed cells), mitose in the cnet tissue and spend most of life there
Fibroblast
principal resident cell
Fibroblast Function
produce components of ECM (see notes)
Fibroblast location
typically near collagen
Active Fibroblasts Where?
actively growing cnct tissue, wound repair; loose connective tissue