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Cavernous tissue refers to blood-filled spaces lined by endothelium and surrounded by smooth muscle. It is present in the erectile tissue of the penis and clitoris . [ 1 ]
A corpus cavernosum penis (singular) (from Latin, characterised by "cavities/ hollows" [2] of the penis, pl.: corpora cavernosa) is one of a pair of sponge-like regions of erectile tissue, which contain most of the blood in the penis of several animals during an erection.
Smooth muscle is grouped into two types: single-unit smooth muscle, also known as visceral smooth muscle, and multiunit smooth muscle. Most smooth muscle is of the single-unit type, and is found in the walls of most internal organs (viscera); and lines blood vessels (except large elastic arteries), the urinary tract , and the digestive tract .
Each crus represents the tapering, posterior fourth of each corpora cavernosa penis; the two corpora cavernosa are situated alongside each other along the length of the body of penis while the two crura diverge laterally in the root of penis before attaching firmly onto either ischial ramus at their proximal end.
Anatomy photo:42:07-0103 at the SUNY Downstate Medical Center - "The Male Perineum and the Penis: The Corpus Spongiosum and Corpora Cavernosa" Image at downstate.edu; Image at downstate.edu; Histology image: 17703loa – Histology Learning System at Boston University; Encyclopedia of Reproduction
The unusual microscopic anatomy of a muscle cell gave rise to its terminology. The cytoplasm in a muscle cell is termed the sarcoplasm; the smooth endoplasmic reticulum of a muscle cell is termed the sarcoplasmic reticulum; and the cell membrane in a muscle cell is termed the sarcolemma. [9] The sarcolemma receives and conducts stimuli.
The corpus cavernosum is homologous to the corpus cavernosum penis in the male. It develops from the genital tubercle in the embryo. [1]The clitoris also has two vestibular bulbs beneath the skin of the labia minora (at the entrance to the vagina), which expand at the same time as the glans clitoridis to cap the ends of the corpora cavernosa.
Partial smooth muscle differentiation of a fibroblastic cell; Activation of a stellate cell (e.g. hepatic Ito cells or pancreatic stellate cells). Loss of contractile phenotype (or acquisition of "synthetic phenotype") of a smooth muscle cell. Direct myofibroblastic differentiation of a progenitor cell resident in a stromal tissue.