Organs

On this page 12 sections
Lungs
- Surface Lining: The lungs are completely enveloped by a serous membrane called the visceral pleura.
- Histopathology: Under a microscope, the visceral pleura is distinctly composed of a single layer of flat mesothelial cells sitting atop a thin, supportive fibrovascular connective tissue layer containing blood vessels and lymphatics. This serous fluid-secreting layer gives the lungs their smooth, lustrous external appearance to prevent friction during breathing.
Liver
- Surface Lining: The liver is covered by a dense connective tissue capsule (Glisson’s capsule), which is itself covered by a layer of visceral peritoneum (mesothelium) over most areas.
- Histopathology Distinction: While it does feature a mesothelial coat, a histopathological diagnosis of an unidentified liver specimen relies heavily on its unique parenchymal architecture—namely, classic hexagonal hepatic lobules, cords of hepatocytes, central veins, and portal triads, rather than a prominent outer fibrovascular mesothelium.
Heart
- Surface Lining: The outer layer of the heart is the epicardium (visceral pericardium), which also consists of an outer mesothelium.
- Histopathology Distinction: While it matches the mesothelial description, the subepicardial fibrovascular layer of the heart uniquely contains a highly characteristic, thick cushion of adipose tissue (fat) alongside large coronary vessels and nerves, all tightly bound to deep layers of thick, branching cardiac muscle (myocardium).
Layers:
The pericardium (the sac enclosing the heart) has layers like an onion:
- Fibrous Pericardium: The tough, outer connective tissue layer.
- Serous Pericardium: The inner double-layered membrane, which splits into:
- Parietal layer: Lines the inside of the fibrous sac.
- Visceral layer (Epicardium): Adheres directly to the outside of the heart muscle itself.
Oral Cavity
- Surface Lining: The oral cavity is lined by a mucous membrane (oral mucosa), not a serous membrane.
- Histopathology Distinction: The oral cavity never contains mesothelium. Instead, because it is an environment exposed to mechanical friction from food, it is lined by a thick stratified squamous epithelium (which can be keratinized on the hard palate/gingiva or non-keratinized on the cheeks and floor of the mouth). It lacks a thin, lustrous mesothelial layer entirely.
Stomach
Parts

Cells
| Cell Type | Location | Primary Secretions | Major Physiological Function |
| Surface Mucous Cells (Foveolar Cells) | Luminal surface and upper gastric pits | High-viscosity mucin, Bicarbonate ions HCO_3^ | Forms a gel-like, alkaline protective barrier that prevents gastric juices from auto-digesting the stomach wall. |
| Mucous Neck Cells | Narrow neck region of the gastric glands | Thinner, soluble, more acidic mucus | Provides localized lubrication and acts as a stem/progenitor pool for replacing surface cells. |
| Parietal Cells(Oxyntic Cells) | Middle and upper body (isthmus/neck) of gastric glands | Hydrochloric acid (HCl), Intrinsic Factor | HCl: Lowers pH to 1.5–3.5 to denature proteins and activate pepsinogen. Intrinsic Factor: Essential for Vitamin B12 absorption in the small intestine. |
| Chief Cells(Zymogenic Cells) | Base (fundus) of the gastric glands | Pepsinogen, Gastric lipase | Pepsinogen: Cleaves into active pepsin under acidic conditions to digest proteins. Gastric lipase: Initiates the breakdown of dietary fats. |
| G Cells(Enteroendocrine) | Basal region / highly concentrated in pyloric antrum | Gastrin (hormone) | Released into the bloodstream to potently stimulate parietal cell HCl secretion and promote mucosal tissue growth. |
| ECL Cells(Enteroendocrine) | Basal region of gastric glands | Histamine (paracrine signal) | Released locally to bind to H2 receptors on neighboring parietal cells, inducing robust acid production. |
| D Cells(Enteroendocrine) | Basal region / pyloric antrum | Somatostatin (hormone/paracrine) | Serves as a crucial negative feedback brake that directly inhibits gastrin and HCl release when luminal pH drops too low (below 2). |
Fundus of stomach
- Muscle Layers: 3 Layers of Smooth Muscle
- Histological Breakdown: The stomach requires intense churning and mechanical breakdown of food. To do this, its muscularis externa is modified to include three distinct smooth muscle layers (ordered from innermost to outermost):
- Inner Oblique Layer: Unique to the stomach; provides the extra directional force needed for churning.
- Middle Circular Layer: Thickens at the pylorus to form the pyloric sphincter.
- Outer Longitudinal Layer: Runs along the length of the organ.
Intestine (Duodenum, Jejunum, Ileum)
- Muscle Layers: 2 Layers of Smooth Muscle
- Histological Breakdown: The entire small intestine follows the classic GI tunic plan. Its muscularis externa consists strictly of two smooth muscle layers:
- Inner Circular Layer: Compresses the lumen to mix chyme.
- Outer Longitudinal Layer: Shortens the tube to propel food forward via peristalsis.
- How to distinguish them individually under a microscope:
- Duodenum: Characterized by prominent Brunner’s glands in the submucosa layer, which secrete alkaline mucus to neutralize stomach acid.
- Jejunum: Features the most well-developed, tall Plicae circulares (circular folds) and long villi, but lacks specific identifying glands in the submucosa.
- Ileum: Characterized by prominent aggregates of lymphoid follicles known as Peyer’s patches in the submucosa (and sometimes extending into the mucosa).
Esophagus
- Muscle Layers: 2 Layers, but with a highly unique gradient of muscle types.
- Histological Breakdown: The muscularis externa of the esophagus also maintains a standard inner circular and outer longitudinal layout, but its tissue composition transitions radically from top to bottom depending on voluntary vs. involuntary control:
- Upper 1/3: Composed exclusively of Skeletal muscle (for voluntary swallowing).
- Middle 1/3: A mixed combination of both Skeletal and Smooth muscle.
- Lower 1/3: Composed exclusively of Smooth muscle as it nears the stomach.
Spleen
The spleen is structurally divided into two distinct functional regions based on its appearance on fresh tissue cuts: the White Pulp and the Red Pulp. These two zones are separated by a narrow interface called the Marginal Zone.
| Feature | White Pulp | Red Pulp |
| Primary Component | Lymphoid tissue (Lymphocytes) | Vascular tissue (Blood-filled spaces & cords) |
| Core Function | Immune response: Activates T & B cells against blood-borne antigens. | Blood filtration: Removes senescent RBCs, stores platelets, recycles iron. |
| Key Microstructures | PALS (T-cells), Nodules (B-cells), Central arteriole | Cords of Billroth (Macrophages), Splenic Sinusoids |
| Circulation Type | Closed circulation | Open circulation (blood empties into tissue cords) |