Grey matter of the spinal cord
Substantia grisea medullae spinalis
Also known as: spinal grey matter, dorsal horn, ventral horn, anterior horn, posterior horn, Rexed laminae, spinal gray matter
The H- or butterfly-shaped central core of the spinal cord. It contains neuronal cell bodies organised into posterior (sensory), lateral (autonomic) and anterior (motor) horns, and into Rexed laminae I–X.
Overview
On each side the grey matter forms a posterior (dorsal) horn, which receives and processes sensory input, and an anterior (ventral) horn, which contains the lower motor neurons. Between thoracic segment 1 and lumbar segment 2 there is also a lateral horn, the intermediolateral cell column, containing sympathetic preganglionic neurons. The two halves are joined by the grey commissure around the central canal.
Rexed divided the grey matter into ten laminae on cytoarchitectonic grounds. Laminae I–VI form the dorsal horn. Lamina I is the marginal zone, which receives nociceptive Aδ and C input. Lamina II is the substantia gelatinosa, the site of the "gate control" of pain and of opioid analgesia. Laminae III–IV form the nucleus proprius (mechanoreception), and lamina V contains wide-dynamic-range neurons involved in referred pain. Lamina VII is the intermediate zone, containing Clarke's nucleus (nucleus dorsalis, C8–L3), the origin of the dorsal spinocerebellar tract, and the autonomic intermediolateral column. Lamina VIII holds commissural interneurons, and lamina IX contains the α and γ motor neuron pools. Lamina X surrounds the central canal.
The motor neurons in lamina IX are arranged somatotopically. Medial groups supply axial (trunk) muscles; lateral groups supply limb muscles and are prominent only in the enlargements. Extensor pools lie anterior (ventral) to flexor pools, and proximal muscles medial to distal ones. Each pool contains large α motor neurons, which innervate extrafusal fibres, and smaller γ motor neurons, which set muscle-spindle sensitivity. Pools are also controlled by Renshaw cells, glycinergic interneurons that mediate recurrent inhibition.
- Location
Central core of the cord, surrounding the central canal throughout its length. It is largest at the cervical and lumbosacral enlargements; lateral horns are present only from T1 to L2.
Parts & subdivisions
- Posterior (dorsal) hornLaminae I–VI. Primary afferents terminate here and synapse on projection neurons (spinothalamic origin in I and V) and on interneurons. Nociceptors end mainly in laminae I–II, and large Aβ touch fibres in III–V.
- Substantia gelatinosa (lamina II)A dense zone of small interneurons that modulates nociceptive input. It is rich in opioid receptors and enkephalinergic interneurons, and is the basis of Melzack–Wall gate control: Aβ input, for example rubbing a bruise, inhibits pain transmission.
- Lateral horn (intermediolateral column, T1–L2)Contains the cell bodies of sympathetic preganglionic neurons. Their axons leave in the ventral roots and white rami communicantes. Damage at T1 can cause Horner syndrome.
- Sacral parasympathetic nucleus (S2–S4)Occupies the equivalent position in sacral segments, but forms no visible horn. It is the origin of the pelvic splanchnic nerves to the bladder, distal colon and erectile tissue.
- Clarke's nucleus (nucleus dorsalis, C8–L3)Lies on the medial base of the dorsal horn in lamina VII. It relays unconscious proprioception from the lower limb and trunk via the dorsal spinocerebellar tract.
- Anterior (ventral) horn (lamina IX)Contains α motor neurons (to extrafusal muscle fibres) and γ motor neurons (to intrafusal spindle fibres). These are the lower motor neurons, the "final common pathway". They are arranged medial for axial muscles, lateral for limb muscles, and ventral for extensors versus dorsal for flexors.
- Renshaw cellsGlycinergic interneurons in the ventral horn. They are excited by recurrent collaterals of α motor neurons and inhibit the same and synergistic motor neurons (recurrent inhibition). Tetanus toxin blocks their transmitter release, producing spasms.
- Grey commissure and lamina XGrey matter around the central canal, crossed by commissural fibres. Lamina X receives visceral afferents.
Anatomy
- Arterial supply
Mostly the anterior spinal artery, through central (sulcal) branches that supply the anterior and lateral horns and the base of the posterior horn. Posterior spinal arteries supply the tip of the dorsal horn.
- Histology
Neuronal cell bodies of very different sizes (α motor neurons up to ≈70 µm), dendrites, unmyelinated and thinly myelinated axons, protoplasmic astrocytes, microglia and capillaries. Nissl staining shows motor neurons with coarse Nissl bodies.
- Development
The alar plate of the neural tube forms the dorsal (sensory) horn and the basal plate forms the ventral (motor) and lateral horns. They are separated by the sulcus limitans.
Function
- Receives and processes all somatic and visceral afferent input entering through the dorsal roots.
- Contains the lower motor neurons that drive skeletal muscle (final common pathway).
- Contains interneuronal networks for reflexes, reciprocal inhibition and central pattern generation.
- Gives rise to sympathetic (T1–L2) and sacral parasympathetic (S2–S4) preganglionic outflow.
- Modulates pain transmission (gate control, descending opioid and monoaminergic inhibition).
Clinical significance
Poliomyelitis and spinal muscular atrophy
Selective destruction of anterior horn cells causes a pure LMN picture: asymmetric flaccid paralysis, areflexia, fasciculations and wasting, with normal sensation. Poliovirus does this; spinal muscular atrophy is the genetic equivalent (SMN1 deletion, the "floppy baby").
Amyotrophic lateral sclerosis (ALS)
Degeneration of anterior horn cells (LMN) and corticospinal neurons (UMN) produces combined wasting, fasciculations, spasticity and hyperreflexia, with sensation and eye movements spared. Riluzole is used as treatment.
Compiled from standard anatomy and physiology references — see the Nervous System sources. For education only; not medical advice.