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Dr. Ali Tahir.  Moist lining of GIT, Nasal passages & body cavities that communicate with the exterior  The mucous membrane of oral cavity is called.

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Presentation on theme: "Dr. Ali Tahir.  Moist lining of GIT, Nasal passages & body cavities that communicate with the exterior  The mucous membrane of oral cavity is called."— Presentation transcript:

1 Dr. Ali Tahir

2  Moist lining of GIT, Nasal passages & body cavities that communicate with the exterior  The mucous membrane of oral cavity is called “Oral Mucosa”  Located anatomically between skin & GIT mucosa & shows some properties of both  Because of its various functions, it is considered an organ Dr. Ali Tahir, M.Phil (Part I)

3  Protection From mechanical forces & abrasion while chewing food & from micro-organisms resident in the oral cavity  Sensation Temperature, Touch, Pain, Taste Receptors for Satisfaction of thirst, Swallowing, gagging, salivation  Secretion Major secretion is saliva Major & minor salivary glands Sebaceous glands are frequently present (upper lip & buccal mucosa) sometimes called Fordyce’s spots but their secretions are insignificant May be an accident of embryologic development Dr. Ali Tahir, M.Phil (Part I)

4 Two parts 1. Outer vestibule (bounded by lips & cheeks) 2. Oral cavity proper (separated from vestibule by teeth & gingiva) Superiorly bound by hard & soft palate Inferiorly by floor of mouth & tongue Posteriorly by pillars of fauces Dr. Ali Tahir, M.Phil (Part I)

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7  Lining Mucosa Constitutes the large part (60%) Soft, pliable  Masticatory mucosa 25% Firm, immobile Gingiva & hard palate  Specialized mucosa Dorsum of tongue, in the form of papillae Unique to oral cavity 15% Dr. Ali Tahir, M.Phil (Part I)

8  Oral mucosa is more deeply coloured compared to skin  B/c of Concentrated & dilated blood vessels Thickness of epithelium Degree of keratinization Amount of melanin  Inflamed mucosa is more red b/c of dilation of blood vessels Dr. Ali Tahir, M.Phil (Part I)

9  Two main components Stratified Squamous Epithelium (oral Epithelium) Lamina Propria  Interface b/w these two is irregular consisting of C.T papillae & rete ridges/pegs  Basal lamina separates the two Dr. Ali Tahir, M.Phil (Part I)

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11 Keratinized Epithelium Hard palate gingiva & tongue  Basal cell layer  Prickle cell layer  Granular cell layer  Keratinized layer Non-keratinized Epithelium Buccal mucosa, floor of mouth, ventral surface of tongue  Basal cell layer  Prickle cell layer  Intermediate cell layer  Superficial cell layer Dr. Ali Tahir, M.Phil (Part I)

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13  A layer of loose fatty or glandular connective tissue may be present between the oral mucosa & underlying bone/muscle  This layer contains blood vessels, nerves & minor salivary glands  Composition of submucosa determines the flexibility of the attachment of oral mucosa to underlying stuructures  Eg, in gingiva & hard palate, oral mucosa is directly attached to periosteum & no submucosa is present. This is called mucoperiostium & is firm and inelastic Dr. Ali Tahir, M.Phil (Part I)

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15  In several regions, nodules of lymphoid tissue consisting of crypts formed by invaginations of the epithelium into the lamina propria are present  Mostly present in posterior parts of oral cavity Lingual tonsils Palatine tonsils Pharyngeal tonsils  Together form Waldeyer’s ring  Small nodules may also be present in soft palate, ventral surface of tongue & floor of mouth Dr. Ali Tahir, M.Phil (Part I)

16  Consist of tightly packed cells called keratinocytes  Maintains its structural integrity by a continuous process of cell renewal  Two types of cell population Progenitor cells Maturing cells  Cells produced by mitosis in the deeper layers (basal & parabasal layers) migrate to the surface layers Dr. Ali Tahir, M.Phil (Part I)

17  Dividing cells are present in clusters at the bottom of epithelial ridges  Progenitor population consists of two groups Stem cells (slow cell cycle)  Produce basal cells & retain proliferative potential of tissue Amplifying cells  Increase the no. of cells available for maturation  After division, each daughter cell recycles in the progenitor population or enters the maturing population  Time required to replace all the cells in the epithelium is called Turnover time Dr. Ali Tahir, M.Phil (Part I)

18  Wide range of estimates have been made  52-75 days for skin  4-14 days for gut  41-57 days for gingiva  25 days for cheek  Non-keratinized epithelium turns over faster than the keratinized Dr. Ali Tahir, M.Phil (Part I)

19  Cancer chemotherapy drugs block the life cycle of cancer cells as well as normal host cells  Cells with short turnover time are most affected. These include Blood cells precursors in bone marrow Intestinal epithelium Oral epithelium  Leads to formation of oral ulcers  In addition, inflammation also affects rate of mitosis Dr. Ali Tahir, M.Phil (Part I)

20  Epidermal growth factor  Keratinocyte growth factor  Interleukin-1  Transforming growth factor α and ß Dr. Ali Tahir, M.Phil (Part I)

21  Present on masticatory mucosa (hard palate, gingiva, parts of dorsal surface of tongue)  Inflexible, tough, abrasion resistant, tightly bound to lamina propria  Process of maturation is called keratinization or cornification Dr. Ali Tahir, M.Phil (Part I)

22  Basal cell layer (stratum basale) Cuboidal or columnar cells containing bundles of tonofibrils. Site of most cell divisions  Prickle cell layer (stratum spinosum) Larger, ovoid cells with conspicous tonofibril bundles, upper part of layer contains membrane-coating granules  Granular cell layer (Stratum granulosum) Flattened cells, keratohyaline granules associated with tonofibrils  Keratinized (stratum corneum) Extremely flattened & dehydrated cells with loss of all organells, cells filled with fibrillar material. If pyknotic nuclie retained, called para-keratinized Dr. Ali Tahir, M.Phil (Part I)

23  Basal cell layer (stratum basale) Cuboidal/columnar cells containing separate tonofilaments  Prickle cell layer (stratum spinosum) Larger ovoid cells containing dispersed tonofilaments, membrane coated granules in upper part of layer  Intermediate layer (stratum intermedium) Slightly flattened cells containing dispersed tonofilaments & glycogen  Superficial layer (stratum superficiale) Slightly flattened cells, dispersed tonofilaments, glycogen, fewer organelle, nuclie Dr. Ali Tahir, M.Phil (Part I)

24  Cells of basal layer are least differentiated cells  Contain organelles & certain structures such as tonofilaments & desmosomes  Tonofilaments are fibrous proteins & belong to the class of intermediate filaments  Aggregate to form bundles called tonofibrils  Chemically represent cytokeratins which are chracteristic constituents of epithelial cells Dr. Ali Tahir, M.Phil (Part I)

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26  Represent a large family of proteins  Classified according to the molecular weight & charge. E.g.. Low molecular weight (40kDa) found in glandular & simple epithelia Intermediate molecular weight found in stratified epithelia High molecular weight (67kDa) in keratinized stratified epithelia  Keratinzed epithelium has Type1, 5, 6, 10, 14, 16  Non-keratinized epithelium has Type 4, 5, 13, 14, 19 Dr. Ali Tahir, M.Phil (Part I)

27  Cohesion b/w cells is provided by protein-carbohydrate complexes produced by epithelial cells themselves  In addition, modifications of adjacent cell membranes of cells called desmosomes provide attachment into which tonofilaments insert  Adherence b/w epith & C.T is provided by hemidesmosomes which attach the cells to basal lamina Dr. Ali Tahir, M.Phil (Part I)

28  Two other types of connections are Gap junctions Tight junctions  Gap junction: Membranes of adjacent cells run closely together separated by a small gap Small interconnections are present Gap junctions allow electric/chemical communication  Tight junction Adjacent cell membranes are tightly apposed Dr. Ali Tahir, M.Phil (Part I)

29  Also called lamellate granules  Are small memrane bound structures about 250nm in size containing glycolipid, originate from golgi complex  Appear in the upper part of prickle layer  They are elongated in keratinized & circular in non-keratinized epithelium  In the upper part of stratum granulosum/intermedium, these granules appear to fuse with superficial cell membrane to discharge their contents into intercellular space Dr. Ali Tahir, M.Phil (Part I)

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31  Cells in the superficial part of granular layer develop a thickening on the intra- cullular aspect of their membrane  It contributes in resistance of keratinized layer to chemical solvents  One of the major constituent of this thickening is a protein called involucrin Dr. Ali Tahir, M.Phil (Part I)

32  Found in keratinized epithelium  Contains keratohyalin granules, which are basophilic granules under light microscope  These are irregular in shape  0.5-1nm in size  Synthesized by ribosomes  Intimately associated with tonofibrils  Facilitate aggregation & formation of cross- links b/w cytokeratin filaments  Proteins making bulk of these granules are called Loricrin Dr. Ali Tahir, M.Phil (Part I)

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34  As the cells of granular layer reach the junction with the keratinized layer, a sudden change occurs  All organelles are lost, including nuclie & keratohyalin granules  Cells dehydrate & assume the shape of hexagonal disks  These are called squames  Squames are lost within days, a process called desquamation & replaced by cells from underlying layers  Limit the colonization of pathogenic micro- organisms  Keratin layer in oral cavity may be upto 20 layers of squames Dr. Ali Tahir, M.Phil (Part I)

35  A slight increase in size occurs in intermediate cell layer  Accumulation of glycogen in cells of surface layer  Occasionally keratohyalin granules are seen but these aren’t associated with tonofilaments  These granules may remain upto the surface layer Dr. Ali Tahir, M.Phil (Part I)

36  Cells in the superficial layer are slightly more flattened  Contain dispersed tonofilaments, retain nuclie & do not dehydrate  Thus are tolerant to compression & distension Dr. Ali Tahir, M.Phil (Part I)

37  Some variation of anatomical locations of keratinized & non-keratinized epithelium may occur  Hyperkeratosis of keratinized oral epithelium is physiological to chronic irritation  Hyperkeratosis of non-keratinized epithelium can be associated with abnormal cellular changes that can lead to cancer  Inflammation of gingiva can lead to loss of keratinization or parakeratinization  These changes are usually reversible when irritant is removed Dr. Ali Tahir, M.Phil (Part I)

38  Oral epithelium is largely impermeable & lacks absorptive capacity  Epithelium at the floor of the mouth, however, is thin & more permeable comparatively (Nitroglycerin to relieve angina pain)  Oral epithelium thus limits the absorption of toxins from micro- organisms except in dentogingival junction Dr. Ali Tahir, M.Phil (Part I)

39  Melanocytes Present in basal layer Lack desmosomes & tonofilaments Dendritic, synthesis of melanin pigment granules (melanosomes)  Merkel Cells Present in basal layer Non-dendritic, tactile sensation  Langerhans cells Dendritic Present in parabasal layer Antigen trapping & processing  Lymphocytes Variable location Inflammatory response B or T cells Dr. Ali Tahir, M.Phil (Part I)

40  Two types of pigmentation is seen in oral mucosa Endogenous Exogenous  Endogenous pigments in oral mucosa are melanin & hemoglobin  Melanocytes are derived from neural crest ectoderm  Enter the epithelium at 11 th week of gestation  Melanosomes are injected into adjacent keratinocytes by long dendritic processes that often pass through several layers of epithelium  Groups of melanosomes can be seen under light microscope, called melanin granules Dr. Ali Tahir, M.Phil (Part I)

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42  Light & dark individuals have the same number of melanocytes, the difference results from the activity of melanocytes  In persons with heavy melanin pigmentaion, melanophages are seen in the connective tissue  In oral mucosa, melanin pigmentation is most commonly seen in gingiva, buccal mucosa, hard palate & tongue & is more in dark skinned individuals Dr. Ali Tahir, M.Phil (Part I)

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44  Oral melanotic macule Increased production of melanin pigment without proliferation of melanocytes  Nevus (Mole) Benign proliferation of melanocytes  Melanoma Malignant tumour of melanocytes Melanoma of oral cavity is aggressive Dr. Ali Tahir, M.Phil (Part I)

45  Exogenous Caused by foreign material introduced locally or systemically One of the most common oral exogenous pigment is amalgum Gives rise to bluish-gray patch called amalgum tattoo Systemic administration of metals such as lead & bismuth can cause gingival margin pigmentation (called Burton’s line) Dr. Ali Tahir, M.Phil (Part I)

46 Stratum distendum is another name for  Submucosa of lining oral epithelium  Prickle layer of non-keratinized epithelium  Superficial layer of Non-keratinized epithelium  Granular layer of keratinized epithelium Dr. Ali Tahir, M.Phil (Part I)

47 The superficial cells of granular layer of keratinized oral epithelium have intra- cellular thickenings to resist chemical solvents containing which proteins? 1. Cytokeratins 2. Glycoproteins 3. Involucrin 4. Filaggrin Dr. Ali Tahir, M.Phil (Part I)

48  Blood flow in oral mucosa is the greatest in which region 1. Soft palate 2. Floor of mouth 3. Gingiva 4. tongue Dr. Ali Tahir, M.Phil (Part I)

49  In infants, Suckling Pad refers to 1. A thickened vermillion zone 2. A thickened intermediate zone 3. A thickened labial mucosa 4. A thickened muco-cutaneous junction Dr. Ali Tahir, M.Phil (Part I)

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