Neuroangiogenesis

Neuroangiogenesis is the coordinated growth of nerves and blood vessels.[1] The nervous and blood vessel systems share guidance cues and cell-surface receptors allowing for this synchronised growth. The term neuroangiogenesis only came into use in 2002[2] and the process was previously known as neurovascular patterning. The combination of neurogenesis and angiogenesis is an essential part of embryonic development and early life.[3] It is thought to have a role in pathologies such as endometriosis,[4] brain tumors,[5] and Alzheimer's disease.[6]

Physiology

Neurovascular patterning

Neurovascular development is the parallel emergence and patterning of the nervous system and the vascular system during embryogenesis and early life.[3][5] Neurovascular congruency appears to be determined by shared molecular patterning mechanism involving axon guidance that involves axonal guidance molecules such as sema3A (semaphorin 3A) and (neuropilin).[7]

Mechanisms

Neuroangiogenic and axonal guidance molecules act on both neuronal growth cones and endothelial tip cells in order to guide growth.[5]

Neuronal growth cones are situated on the tips of nerve cells and are responsive to different factors, both positive and negative. Growth of the neuron occurs by an extension of the actin (red in image) and microtubule (green in image) cytoskeleton.[8]

Neuronal growth cone

Tip cells found at the extremity of the developing blood vessel control adjacent endothelial cells to direct growth. Tip cells have receptors and ligands via which they respond to local neuroangiogenic factors.[8]

Neurogenic factors

There are many neuroangiogenic factors, some of which act to promote neuronal growth and vice versa.[5] The table shows examples

Neuroangiogenic factorEffect on neuronEffect on vascular endothelial cellsReceptor/LigandOrigin
IGF-1Promotion of neurogenesis and synaptogenesisEC proliferation, migration, and differentiationLigandLiver cells
bFGFProliferation of cortical progenitors and neurogenesisEC proliferation, migration, and differentiationLigandAdipocytes
NGFNeuron survival, differentiationPromotion of angiogenesis and arteriogenesis in ischemic hindlimbsLigandMultiple
NeuropilinAxon guidanceSynergistic action of VEGF165 in EC migration and proliferation
Vascular development		ReceptorTarget cell
VEGFNeuronal development and patterning, and has neurotrophic and neuroprotective effectsInduces angiogenesis, promotes endothelial cell survival, proliferation and migrationLigandMultiple

Pathology

Neuroangiogenesis is implicated in a number of pathologies, including endometriosis,[4] brain tumors,[5] and senile dementias, such as Alzheimer's disease.[6] Each of these incurs a significant cost for the healthcare industry, meaning that complete understanding of processes involved – including neuroangiogenesis – is necessary to enable development of functional treatments.[5][9]

Endometriosis

Endometriosis is a common gynaecological disease caused by endometrial tissue implanting outside the uterus, a symptom of which is chronic pelvic pain. The formation, growth and persistence of these implants are dependent upon angiogenesis to increase the supply of blood vessels. The resulting increase in blood flow may correlate directly with pain symptoms. One possible explanation for this is the simultaneous growth of neurons into these areas alongside blood vessels through neuroangiogenesis.[4]

Brain tumors

Brain tumors, such as glioblastoma multiforme, are characterized by dense vascularity associated with high expression of the proangiogenic factors, VEGF and interleukin 8.[5]

Brain injury

Following ischemic stroke or traumatic brain injury, angiogenesis supports oxygen and nutrient re-supply to injured tissue, and stimulates neurogenesis and synaptogenesis, particularly in the ischemic penumbra.[5] Neuroangiogenesis is finely regulated and sequential, involving proliferation and migration of endothelial cells to restore blood-brain barrier function, recruitment of pericytes, and stabilization new blood vessels, a process dependent on upregulation of proangiogenic factors, such as VEGF and angiopoietin-1.[5]

Alzheimer’s disease

A condition possibly resulting from a reduction in neuroangiogenic factors is Alzheimer’s disease. Without continued neuroangiogenesis during aging, areas of the brain may no longer have the full complement of functional capillaries and hence, by inference, cerebral blood flow and cognitive ability decline.[5][6] This condition of reduced neuroangiogenesis and lower capillary density during senescence, possibly involving impaired regulation of angiogenic factors by hypoxia, could be a vascular basis for Alzheimer's disease.[5][6][10]

See also

References
  1. Greaves, E; Collins, F; Esnal-Zufiaurre, A; Giakoumelou, S; Horne, A. W.; Saunders, P. T. (2014). "Estrogen receptor (ER) agonists differentially regulate neuroangiogenesis in peritoneal endometriosis via the repellent factor SLIT3". Endocrinology. 155 (10): 4015–26. doi:10.1210/en.2014-1086. PMID 25051436.
  2. Park; et al. (2002). "Delayed Up-regulation of Vascular Endothelial Growth Factor and flk-1 after Global Cerebral Ischemia in Mongolian Gerbil -Possible roles in neuroangiogenesis?" (PDF). Korean Neurological Association. Retrieved 30 September 2015.
  3. Bautch, V. L.; James, J. M. (2009). "Neurovascular development: The beginning of a beautiful friendship". Cell Adhesion and Migration. 3 (2): 199–204. doi:10.4161/cam.3.2.8397. PMC 2679887. PMID 19363295.
  4. Asante, A; Taylor, R. N. (2011). "Endometriosis: The role of neuroangiogenesis". Annual Review of Physiology. 73: 163–82. doi:10.1146/annurev-physiol-012110-142158. PMID 21054165.
  5. Vallon M, Chang J, Zhang H, Kuo CJ (2014). "Developmental and pathological angiogenesis in the central nervous system". Cell Mol Life Sci. 71 (18): 3489–3506. doi:10.1007/s00018-014-1625-0. PMC 4165859. PMID 24760128.CS1 maint: uses authors parameter (link)
  6. Ambrose, C. T. (2012). "Neuroangiogenesis: A vascular basis for Alzheimer's disease and cognitive decline during aging". Journal of Alzheimer's Disease. 32 (3): 773–88. doi:10.3233/JAD-2012-120067. PMID 22850316.
  7. Bates, D; Taylor, G. I.; Minichiello, J; Farlie, P; Cichowitz, A; Watson, N; Klagsbrun, M; Mamluk, R; Newgreen, D. F. (2003). "Neurovascular congruence results from a shared patterning mechanism that utilizes Semaphorin3A and Neuropilin-1". Developmental Biology. 255 (1): 77–98. doi:10.1016/s0012-1606(02)00045-3. PMID 12618135.
  8. Park, J. A.; Choi, K. S.; Kim, S. Y.; Kim, K. W. (2003). "Coordinated interaction of the vascular and nervous systems: From molecule- to cell-based approaches". Biochemical and Biophysical Research Communications. 311 (2): 247–53. doi:10.1016/j.bbrc.2003.09.129. PMID 14592405.
  9. Morotti, M; Vincent, K; Brawn, J; Zondervan, K. T.; Becker, C. M. (2014). "Peripheral changes in endometriosis-associated pain". Human Reproduction Update. 20 (5): 717–36. doi:10.1093/humupd/dmu021. PMC 4337970. PMID 24859987.
  10. Ambrose, C. T. (2016). "The Role of Capillaries in the Lesser Ailments of Old Age and in Alzheimer's Disease and Vascular Dementia: The Potential of Pro-Therapeutic Angiogenesis". Journal of Alzheimer's Disease. 54 (1): 31–43. doi:10.3233/JAD-160303. PMID 27392865.
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