Crosstalk of Brain and Bone-Clinical Observations and Their Molecular Bases.
Ellen OttoPaul-Richard KnapsteinDenise JahnJessika AppeltKarl-Heinz FroschSerafeim TsitsilonisJohannes KellerPublished in: International journal of molecular sciences (2020)
As brain and bone disorders represent major health issues worldwide, substantial clinical investigations demonstrated a bidirectional crosstalk on several levels, mechanistically linking both apparently unrelated organs. While multiple stress, mood and neurodegenerative brain disorders are associated with osteoporosis, rare genetic skeletal diseases display impaired brain development and function. Along with brain and bone pathologies, particularly trauma events highlight the strong interaction of both organs. This review summarizes clinical and experimental observations reported for the crosstalk of brain and bone, followed by a detailed overview of their molecular bases. While brain-derived molecules affecting bone include central regulators, transmitters of the sympathetic, parasympathetic and sensory nervous system, bone-derived mediators altering brain function are released from bone cells and the bone marrow. Although the main pathways of the brain-bone crosstalk remain 'efferent', signaling from brain to bone, this review emphasizes the emergence of bone as a crucial 'afferent' regulator of cerebral development, function and pathophysiology. Therefore, unraveling the physiological and pathological bases of brain-bone interactions revealed promising pharmacologic targets and novel treatment strategies promoting concurrent brain and bone recovery.
Keyphrases
- bone mineral density
- white matter
- resting state
- soft tissue
- bone loss
- cerebral ischemia
- functional connectivity
- bone marrow
- bone regeneration
- postmenopausal women
- public health
- healthcare
- multiple sclerosis
- mental health
- dna methylation
- blood pressure
- radiation therapy
- bipolar disorder
- cell death
- brain injury
- gene expression
- single cell
- climate change
- rectal cancer
- single molecule