This reminded me of a topic I posted. You’d also probably be looking at muscle involvement as well.
Retinoic acid induces alveolar regeneration in the adult mouse lung
European Respiratory Society – 1 Jan 04
Recent data suggests that exogenous retinoic acid (RA) can induce alveolar regeneration in a mouse and a rat model of experimental emphysema and disrupted alveolar development. This may be because RA is required during normal alveolar development and…
Recent data suggests that exogenous retinoic acid (RA) can induce alveolar regeneration in a mouse and a rat model of experimental emphysema and disrupted alveolar development. This may be because RA is required during normal alveolar development and the subsequent provision of RA reawakens the gene cascades used during development.
Here, additional evidence that RA is required during alveologenesis in the mouse is provided by showing that disulphiram disrupts this process. A further model of disrupted alveolar development using dexamethasone administered postnatally is then described, and it is further shown that RA administered to these adult mice restores the lung architecture to normal.
This is a little off topic but again the keyword is regeneration.
1.3.4 Retinoic Acid
RA has been found to have a role in neural patterning (Wilson et al., 2004) in
development. In the chicken spinal cord, RA treatment increases motor neuron
generation and increases the proliferation of ventral progenitors (Sockanathan and
Jessell, 1998). Treatment of RA in zebrafish embryos also increases the number of
motor neurons generated during development (Ryu et al., 2015) and biases the
proliferating progenitors towards motor neuron fates at the expense of GABAergic
interneurons (Kong et al., 2018). It is necessary for adult neurogenesis in mammals
(Jacobs et al., 2006) and is used extensively in vitro to direct neuronal differentiation
of stem cells (Tonge and Andrews, 2010; Tan et al., 2015). The RA signalling
pathway, such as receptors (rarab, rxrga) and downstream genes (crabp2a, cyp2ba),
is upregulated in the adult zebrafish spinal cord after a lesion (Reimer et al., 2009).
Raldh2 is increased in mammalian spinal cord after injury in NG2+ cells (Mey et al.,
2005; Kern et al., 2007). No studies so far have investigated the functional role of RA
in neuroregeneration in the spinal cord.