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43 Cards in this Set
- Front
- Back
Esophageal Tissue Layers
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MUCOSA: **esophageal folds of mucosa run parallel to long axis of organ - not encirciling lumen.
- EPITHELIUM: THICK layer: nonkeratinized stratified squamos epithelium continuous with pharynx -> renews itself through mitosis of stem cells in basal layer - Langerhan cells: antigen presenting functions - for defense of surrounding tissues LAMINA PROPRIA: papillae undulates into epithlium to increase surface area between the two tissues to bind them together - Well Vascularized!!: rich in capillaries in nerves (if epithelium is broken, get bleeding from this rich bed of blood vessels) - not very cellular - accumulations of diffuse lymphatic tissue MUSCULARIS MUCOSA: only Longitudinal smooth muscle!! - thin and discontinuous in upper esophagus -> thicker and more continuous in lower esophagus SUBMUCOSA: loose CT - esophageal MUCOUS glands - rich elastic fiber network: impt for reclosure of lumen follow peristalsis of food - Submucosal Plexus (Meissner's) -lymphatic tissues, adipose cells, nerves, and BV's MUSCULARIS EXTERNA: 2 layers - Upper esophagus: only skeletal muscle! - voluntary control - Middle: both smooth and skeletal; smooth appears first in inner circular and then eventually outer long. until all smooth! - Lower: all smooth - involuntary control - Auerbach's plexus - between 2 layers SEROSA/ADVENTITIA: - Cervical/Thoracic (above diaphragm): Adventitia - After Diaphragm: Serosa (peritoneum) |
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Esophagus-Stomach Junction
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Esophagus -> LES -> Stomach
Esophagus: nonkeratinized stratified squamos epith. LES: NO thickening of muscularis externa b/c physiological sphincter under ANS control (& some function by diaphgram constriction) Stomach: simple columnar epithelium, 2 layers of muscularis mucosae, 3 layers of muscularis externa: middle circular, outer longit., inner oblique: facilitates churning and persitalsis |
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Stomach Layers
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MUCOSA: thick layer, smooth when relaxed but has Rugae when contracted (incorporates into submucosa that flatten when distended)
**Epithelium: simple columnar Surface Mucous Cells (NOT goblet cells) - Gastric pits: invaginations of surface mucous columnar epith. *where cells that are for replacement of damaged luminal cells are found -base of pits RECEIVE INFO FROM LONG TUBULAR GLANDS that differ in stomach regions **Lamina Propria: infiltrated with GLANDS! **Muscularis Mucosae: 2 layers - forms MUCOSAL RIDGE SUBMUCOSA: - NO GLANDS (unlike esophagus and duodenum) - Meissner's plexus present - Rugae MUSCULARIS EXTERNA: 3 layers to maximize churning and peristalsis: inner oblique, middle circular, outer longitudinal - Auerbach's plexus |
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Glands beneath Gastric Pits
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glands empty into the gastric pits -> lumen of stomach
- glands found in MUCOSA LAYER: takes up most of lamina propria - beneath Gastric pits |
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Cardiac Glands
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-Cardiac: where esophagus enters stomach (small part)
- simple or branched tubular glands that are the same length as the gastric pits - Predominate in MUCUS SECRETING cells (differ from surface mucous cells & neck cells) - Parietal Cells: secrete HCl and IF into lumen and HCO3- into lamina propria |
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Gastric Glands
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MAIN STOMACH GLANDS!! - glands of Fundus and Body that secrete Digestive Agents
- Branched Tubular glands - 3-7 glands empty into 1 gastric pit base 5 CELL TYPES in gland walls: 1) PARIETAL(oxynitic cell): - secrete HCl and IF - large, oval, and eospinophilic plasma (pumps ions from the cell into lumen of gland) - bulge laterally into surrounding CT - mainly in UPPER part of glands, up into the base of pits 2) CHIEF (peptic or zymogenic) cell: produce pepsiongen and weak lipase for pancreas - round nucleus, BASOPHILIC cytoplasm due to ribosomes - typically artifactually light staining - usually at BASE of gland 3) MUCOUS "neck" cells: - concentrated in neck (superficial area) of glands *DIFFER FROM SURFACE mucous cells: - secrete soluble mucus vs. surface mucous cells that are INsoluble) -shorter than surface mucus cells - less mucinogen in apical cytoplasm (mucinogen + h20 = mucin) but mucinogen is what stains! 4) STEM cells: small columnar cells in UPPER region of glands and base of pits - few in quantity but give rise to: 1) all cells of gland 2) surface mucous cells (those residing in pits) 5) ENTEROENDOCRINE (EEC): aka enterochromaffin/argentaffin cells: - single endocrine cells dispersed near BASE OF GLAND - endocrine secretion! - cytosplasmic SPHERICAL BASAL granules that contain hormone - secretions important for motility and glandular secretions ie) glucagon, somatostatin, gastrin **1 cell secretes 1 hormone! |
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Pyloric Glands
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3 Cell Types: no parietal or chief cells!
1) MAINLY mucous cells - mucinogen-PALE-takes up most of cell cytoplasm volume, NUCLEUS PUSHED FAR TO BASE! 2) EEC's: G cells and D cells: light eospinophilic (looks like parietal cell but nucleus more in center) **ENTER LOCAL CIRCULATION OF GI 3) some stem cells Short length glands compared to long Gastric glands |
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Pyloric Stomach-Duodenum Junction (Pyloric Sphincter)
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Fundus of Stomach -> Duodenum of Small Intestine
STOMACH FUNDUS: - uniform surface mucus cells - undulating muscularis mucosae that follows mucosa SUBMUCOSA: - rugae - folds of submucosa that flatten with distension - rich in caps/BV in CT PYLORIC SPHINCTER: anatomical! thickening of stomach's muscularis externa's Inner circular and oblique layers! (hypertrophy) -closes down with each peristalic contraction to allow only fluids and small material to pass through to small intestine - RETROGRADE movement: allows churning of food and homogenization of chyme in stomach! DUODENUM: - Submucosa - BRUNNER's GLANDS: pure mucous submucosal glands |
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Rugae
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Infolding of submucosa
1) In stomach 2) Esophagus 3) Large Intestine **serves to increase surface area and allow for storage of food - flattens out when food enters (distension) VS PLICAE CIRCULARIS in small intestine - circular folds that are always there! |
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GI TRACT COMPONENTS
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22-25 feet long hollow tube
- 4 separate organs that connect oral cavity with anus 1) Esophagus: 1 foot 2) Stomach: 1 foot 3) Small Intestine: 15 feet 4) Large Intestine: 5 feet - ENTERIC NS |
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FUNCTION of GI
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1) Mechanical Propulsion: peristalsis
2) Digestion: physical and chemical breakdown 3) Absorption: uptake into system of needed substances 4) Protection: defenses that prevent or limit invasion by ingested viruses and bacteria, also protection against self digestion |
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ENTERIC NS
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- GI has efferent neurons, afferent, and inerneurons
- can carry out reflexes in absence of CNS input - motor neurons control intestinal muscles and peristaliss and churning of intestinal contents - 2 TYPES OF GANGLIA: 1) Auerbach's myenteric plexus 2) Meissner's submucosal plexus |
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Lower Esophageal Sphincter
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- Physiological sphincter: no pronounced thickening of inner circular layer at junction but a specialized szone of somewhat thickened circular muscle surround esophagus as it traverses the diaphgram and continues into abdomical regiion
- this thickened circular muscle is maintained under TONIC contraction except w/ swallowing - controlled by Eneteric NS and protects against reflux of acid from stomach - diaphgram also contributes to esophageal sphincter function **becomes in lower part under diaphgram, part of abdominal pressure!! harder to reflux! |
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Hiatus Hernia
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Bulging of the stomach through the diaphragm into thoracic cavity:
- can cause ACID REFLUX BECAUSE MORE FAVORABLE GRADIENT!! |
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Protective Mechanisms of the Esophagus
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1) thick stratified nonkeratinized squamos epithelium of mucosa
**renewed every 5-7 days from basal stem cells 2) dispersed lymphatic tissue in lamina propria and submucosa **B lymphocytes from plasma cells that produce antibodies **more lymphatic tissue near esophageal glands because have simple cuboidal spithelium at ducts |
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Swallowing/Problems with Esophagus
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Problems with Esophagus will present as Dysphagia:
1) Physical Blockage: lumen growth causes impingement -> malignant! 2) Aclasia: no innervation from myenteric plexus, so no sympathetic innervation and no relaxation of LES - tonically active so food gets stuck in esophagus (dilated esophagus) |
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Esophagus: MAIN FUNCTION
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1) Propulsion
2) Protection |
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Stomach: Main Function
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1) Digestion - physical and chemical
2) Propulsion 3) Protection (also from self!) |
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Mucosal Ridges
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Formed from smooth muscle fibers in muscularis mucosa of Stomach extending into interglandular lamina propria
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Protection mechanisms of Stomach
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1) Surface Mucous Cells - protect from normal "wear and tear"
2) Secreting Mucous cells in Cardiac region and Pyloric area 3) HCO3- from Parietal Cells: neutralize any H+ that may leak through 4) replacing surface cells via stem cells every 3-5 days 5) if above mech's DONT WORK --> Rapid Re-Epithilization |
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Rapid Re-Epithelization:
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- occurs when surface mucus cells are lost or HCO3- doesn't protect cells
- Migration of Surface mucous cells located WITHIN gastric pits (protected b/c exposed to less toxin) -> surface to replace damage surface mcuous cells - Simple Columnar Epithelium Surface Mucus Cells -> Squamos Epithelial Lining (20 min) --> back to columnar cells (if not constantly damged) ** if constant damge: no repopulation of by stem cells and surface epithelial cells lost --> ULCERS due to lack of ability of cells in pits to re-epithelialize surface |
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Mucosal Geometry of Large Intestine
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Epithelium:
-Intestinal Glands = CRYPTS OF LIEBERHUKHN - Enterocytes have Microvill (but less developed as those in small intestine) Submucosa: 1) Meisner's plexus 2) Rugae Muscularis Externa: 1) Auerbach's |
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Mucosal Geometry of SMALL intestine
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Epithelial Layer:
- Microvilli - folds in enterocyte plasmolemma with actin filaments (cell membrane) - Enterocytes - Terminal Bar/Web - Intestinal Glands = Crypts of LIberkhukhn Lamina Propria: - Intestinal villi: highly vascularized folds of lamina propria that extend up into lumen --> increases SA of small intestine to increase absorption Muscularis Mucosae: discontinous throughout small intestine because of structures such as 1) Brunners glands - submucosal glands in duodenum 2) Peyer's patches - GALT in ileum (SUBMUCOSA!!) Submucosa: 1) Plicae Circulares (Valves of Kerkring): similar to rugae but don't disappear with distension of lumen. - Function: slow the passage of intestinal contents and increase absoprtive surface area. - Large in upper small intestine and diminishes in frequency towards distal ileum. 2) Brunner's glands - mucosal glands!! 3) Meisnesser's plexus (also Auerbach's) |
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Cells of Luminal Epithelium: COLON
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1) Enterocytes - absorptive cells (less frequent than in Small intestine
- responsible for ionic exchange and other transepithelial transport activities (ie. ionic regulation and h20 resoprtion) - Enteroctyes have apical microvill 2) Goblet cells: secrete mucus --> more found in distal small intestine than in duodenum **for fecal lubrications - very abundant in lower colon and rectum! 3) M (microfold) cells: flattened cells with basal folds that overlies GALT - transport stuff from lumen to lymphocytes in gut 4) Stem cells: lie in middle of Intestinal glands - migrate up and down to replace mature cells 5) EEC: solitary hormone produce cells located throughout epithelium but mainly in base of gland - triangular shaped, basal zymogen granules (secrete hormones to blood - each cell -> different hormone! |
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Small Intestine Luminal Epithelium Cells
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Intestinal Villi have terminal bars/webs so material needs to pass THROUGH ENTEROCYTES & not between them.
CELLS: 1) Enterocytes: highest in frequency (Duodenum > colon) 2) Goblet cells: lowest in frequency (Colon > Duodenum) EXOCRINE cell 3) EEC (APUD): present at base of crypts and on surface of intestinal villi - AMINE precursor uptake and decarboxylation 4) M cells 5) Stem Cells 6) PANETH CELLS: EXOCRINE cells - in BASE of glands/crypts - eosinophilic granules packing apical cytoplasm - lysozyme: - stains eosinophilic - Zinc - binds Pb-Hematoxylin as black **BREAKDOWN PRODUCTS BROUGHT TO M CELLS -> LYMPHOCYTES = Immune exclusion |
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Central Lacteals & Pathway of lipids
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present in SMALL INTESTINE - INTESTINAL VILLI
- lymphatic vessels that transport CM from intestines and deliver lipids to circulation PATHWAY of LIPIDS (CM):GOES THROUGH LYMPHATIC CIRCULATION FIRST -> SYSTEMIC CIRCULATION -> PORTAL CIRCULATION (intestine, heart, liver) CM made in Small intestine -> central lacteal -> lymphatic ducts -> thoracic ducts -> inferior/superior vena cava-> hepatic artery -> liver **CENTRAL LACTEAL - WITHIN THE BASAL SIDE OF ENTEROCYTES IN INTESTINAL VILLI |
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Mesentery
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pathway for blood vessels and nerves that go to and from the Small intestine
*attached jejunum and ileum to abdominal wall |
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Differences in Submucosa of Small Intestine: Duodenum vs. Jejunum vs. Ileum
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DUODENUM
1) Brunner's glands 2) high frequency of enterocytes 3) high frequency of Plicae Circularis JEJUNUM: 1) NO Brunner's glands or Peyer's patches ILEUM: 1) Peyer's patches - 10 lymph nodules - patches of follicles and interfollicular lymphoid tissue = GALT (specific to ileum: always present!!) 2) INTRAepithelial lymphocytes: migrated from underlying lymph tissues ie. M cells: always overlying GALT - important for TRANSPORT (not APC's or macrophages) 3) Unnamed GALT |
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Ileoceccal Valve
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Ileum -> Cecum
Ileum: MUCOSA: - intestinal villi: rapped mucosal lining - Crypts of Liberkuhn ILLECOCECCAL VALVE: no sphincter! - thickening fold of tissue - extension muscularis externa of colon wall - in TONIC contraction by SYMPATHETIC innervation - VALVE PREVENTS REFLUX from cecum to ileum - may act as a SPHINCTER: prevent ileal contents into cecum Colon: MUCOSA: - smooth mucosal lining - simple tubular glands (no microvilli) |
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Large Intestine: Colon->Rectum
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SURFACE EPITHELIUM:
- Intestinal glands - crypts - high frequency of GLOBLET CELLS (highest in rectum) - low frequency of enterocytes Muscularis Externa: - Taeniae Coli: 3 evenly spaced longitudinal bands of outer longitudinal muscle (but not present in rectum!!) |
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Large Intestine: Rectoanal Junction
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BASICALLY WHERE PECTINATE LINE IS (right before start of External sphincter which does overlap with internal anal)
AT JUNCTION: - termination of muscularis mucosae - dense irregular CT in lamina propria - Submucosa and lamina propria - highly vascular!! ie) NEAR OR IN AREA OF EXTERNAL SPHINCTER has HEMORRHOIDAL veins --> hemororhoids!) **RECTUM -part of large intestine: dilated portion of it - HIGHEST frequency of GOBLET cells - NO Taeniae Coli **ANUS INTERNAL ANAL SPHINCTER: hypertrophy and extension of circular layer of SMOOTH MUSCLE e of muscularis externa PECTINATE LINE: site of embryonic anal membrane (Endoderm -> ectoderm); WITHIN ANAL CANAL - SIMPLE COLUMNAR EPITH. -> Stratified squamos NON keratinized epith (short transition zone) --> STRAT SQUAMOS KERTINZED EPITH. (skin beyond anus!) EXTERNAL ANAL SPHINCTER: circumferential RING OF SKELETAL MUSCLE - not continuous with Internal sphincter |
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Rectum Anal Canal
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- includes Pectinate Line
- plus or minus 4cm of pectinate line |
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Hemorrhoids
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2 plexuses veins within Submucosa become distended and varicose
**IN OR NEAR AREA OF EXTERNAL ANAL SPHINCTER! 1) Internal Hemorrhoidal Plexus: above Pectinate line (between rectum and anus; and where intouernal and external sphincter overlap!) 2) External Hemorrhoidal Plexus: occurs at junction of anal canal and anus |
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Crypts of Lieberkuhn
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= Intestinal Glands (both small and large intestine)
- have stem cells near the base of the pits that renew surface epithelium every 3-5 days and Paneth Cells & EEC cells that turn over every 3-5 weeks - cells in these crypts secrete salts and H20 |
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Digestive Mechanisms of Small Intestine:
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1) Enzymes from Pancreas - complete digestion of chyme from stomach
a) Amylase b) Lipase c) Peptidases d) Trypsinogen -> trypisin via Enterokinase from Enterocyte glycocalyx |
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Bile Absorption (why important?)
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- water and bile absorbed in samll intestine
1) liver only produces 3g bile a day but need 10 g for digestion so need to recycle bile for re-processing in liver and gall bladder! --> complete digestion of fat 2) bile absorption facilitates h20 absorption --> if problem then diarrhea! |
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Protective Mechanisms of Small Intestine
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1) protect from SELF DIGESTION from acidic chyme!!
- Glycocalyx: glycoproteins surrounding microvilli of enterocytes - Goblet cells: alkaline secretions coating epithelial surface - Brunner's glands: alkaline secretions from duodenal glands - Bile: secreted from liver - alkaline and buffers acidic chyme - pancreatic fluid: secreted with pancreatic enzymes into lumen of duodenum; alkaline **NET: secrete alkaline fluid! 2) protection from INVASION OF EXOGENOUS ORGANISMS: - Lymphoid tissue: 1. Intraepithelial lymphoid tissue in mucosa 2. diffuse lympoid tissue in lamina propria 3. isolated lympoid nodules in lamina propria/submucosa 4. circular aggregations of lymph nodules in ileum (Peyer's Patches - GALT) 5. Paneth cells - secrete lysozyme: lyses walls of bacteria that have survived through the base of the crypts --> IgA **principal function is "IMMUNE EXCLUSION" - TO DELIVER ANTIGENIC MATERIAL TO M CELLS -> lymphocytes -> immune response triggered > plasma cells (within in Peyer's patches) SECRETE IgA-type antibodies sepcific (gi tract -> lymph -> gi) |
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Appendicitis
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acute inflammation of appendix
1) ULCERATION of mucosa - abdominal pain 2) PERITONITIS: inflammation spreads -> bursting of appendix |
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Appendix
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- filled with diffuse lymphatic tissue and with nodules (looksl ike GALT but NOT peyer's patches)
- lymph nodules contain antibody producing plasma cells and immunocompotent B and T lymphocytes - no INTESTINAL VOLUME like in small intestine |
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Anal (Rectal Columns) = columns of Morgagni
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- 1st part of anal canal formed into longitudinal folds --> allow gas to pass out while feces retained
- where columns end = pectinate line (simple columnar epith -> stratified squamos non keratinized epith. - stratified squamos non keratinized epith -> keratinized at anus to skin |
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External Sphincter
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addition of skeletal muscle layer (not continuous with circular layer of muscularis externa that thickens in Internal anal sphincter)
- overlaps with some of internal anal sphincter! - voluntary control!! |
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Immune Exclusion
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-of SMALL INTESTINE
MECHANISM: M-cells in the epithelium trans- port antigens from the lumen to underlying lymphocytes capable of initiating an immune response. Lymphocytes from the stimulated clone of effector and mem- ory cells then return to the GI tract. In the GI tract plasma cells secrete IgA-type antibodies specific for the antigen previously presented to their lymphocyte precursors. This immunoglobulin is taken up actively by the columnar absorp- tive cells that bind it to the glycocalyx where it protects by “immune exclusion”. |
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HEV
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specialized post capillary venule in GALT and lymph nodes that is the location of where lymphocytes REENTER FROM BLOOD TO LYMPH!!
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