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        <datestamp>2026-09-21T09:18:17Z</datestamp>
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          <dc:title>Supporting Data for "Multipotent neural stem cells are found in the mouse periphery and contribute to early peripheral neural development"</dc:title>
          <dc:creator>Wan Xu (9391988)</dc:creator>
          <dc:subject>Peripheral nervous system</dc:subject>
          <dc:subject>Neurosciences not elsewhere classified</dc:subject>
          <dc:subject>Foetal development and medicine</dc:subject>
          <dc:subject>neuroscience</dc:subject>
          <dc:subject>developmental biology</dc:subject>
          <dc:subject>neural stem cells</dc:subject>
          <dc:subject>neurodevelopment</dc:subject>
          <dc:subject>stem cell biology</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;Conventional models of mammalian development hold that neural stem cells (NSCs) are restricted to the central nervous system. In this thesis, we identify and characterize a population of peripheral NSCs (pNSCs) present in the neonatal mouse periphery and, to a limited extent, in adult tissues. These cells can be isolated from multiple peripheral tissues, express canonical NSC markers, and exhibit molecular and functional properties closely resembling those of brain-derived NSCs. Lineage-tracing analyses further demonstrate that pNSCs originate from Sox1-positive neuroepithelium, sharing the same developmental origin as conventional brain NSCs, rather than that of the neural crest. Single-cell RNA sequencing of pNSCs in situ resolves quiescent and active NSC clusters that show strong transcriptional similarity to brain NSCs. Furthermore, these cells exhibit low correlation with other tissue-resident stem cell populations in the corresponding tissues, indicating that they are indeed authentic endogenous NSCs.&lt;/p&gt;&lt;p dir="ltr"&gt;We show that pNSCs emerge during early neurulation from the entire rostrocaudal neural tube and migrate broadly into embryonic peripheral tissues. Through extensive immunostaining and single-cell sequencing of near-term embryonic tissues, we demonstrate that pNSC progeny contribute to multiple peripheral cell populations, including neurons and a smaller fraction of glial cells, across diverse tissues. Postnatal mapping further revealed marked tissue- and region-specific differences in pNSC persistence. In most peripheral tissues, pNSCs were detected only transiently and declined rapidly after birth, whereas the lung retained Sox1-positive pNSC clusters from neonatal stages into adulthood, identifying it as a uniquely stable peripheral niche for long-term pNSC maintenance. Upon bronchial injury, lung pNSCs exhibited limited Ki67 expression and gave rise to Sox1-negative, non-neuronal progeny, suggesting a restricted regenerative response in the endogenous lung niche.&lt;/p&gt;&lt;p dir="ltr"&gt;Functional analyses further showed that peripheral tissue-derived pNSCs can be expanded in vitro for extended periods and are capable of differentiation into neurons, astrocytes, and oligodendrocytes, confirming their multipotency.&lt;/p&gt;&lt;p dir="ltr"&gt;Collectively, these findings establish pNSCs as a neuroepithelium-derived stem cell population with broad peripheral distribution during development, tissue-dependent postnatal persistence, and context-dependent responses to injury in the lung. Our findings expand current understanding of mammalian NSC development and offer a more accessible source of endogenous NSCs with potential relevance to regenerative medicine.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-21T09:18:17Z</dc:date>
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          <dc:identifier>10.25442/hku.33276978.v1</dc:identifier>
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          <dc:rights>CC BY-NC 4.0</dc:rights>
          <dc:rights>Open Access after 2028-08-18</dc:rights>
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