TY - JOUR
T1 - Some distal limb structures develop in mice lacking Sonic hedgehog signaling
AU - Kraus, Petra
AU - Fraidenraich, Diego
AU - Loomis, Cynthia A.
N1 - Funding Information:
The authors thank C.X. Tong and M. Birgé for excellent assistance, H. Westphal for kindly providing the Shh-deficient line, and A. Joyner, M. Nagashima, T. Lufkin, H. Makarenkova, R. Kimmel, H. Park, K. Briegel and H. Sun for sharing mice, probes and experiences. Especially we thank A. Joyner and D. Yelon for interesting discussions and H. Makarenkova, T. Lufkin, C. Basilico and M. O'Guin for comments on the manuscript. P.K. and C.L. were supported by the Dermatology Foundation and the March of Dimes Foundation, respectively.
PY - 2001
Y1 - 2001
N2 - Patterning of the limb is coordinated by the complex interplay of three signaling regions: the apical ectodermal ridge (AER), the zone of polarizing activity (ZPA), and the non-ridge limb ectoderm. Complex feedback loops exist between Shh in the ZPA, Bmps and their antagonists in the adjacent mesenchyme, Wnt7a in the dorsal ectoderm and Fgfs in the AER. In contrast to the previously reported complete absence of digits in Shh(-/-) mice, we show that one morphologically distinct digit, with a well-delineated nail and phalanges, forms in Shh(-/-) hindlimbs, while intermediate structures are severely truncated and fused. The presence of distal autopod elements is consistent with weak expression of Hoxd13 in Shh(-/-) hindlimbs. Shh(-/-) forelimbs in contrast have one distal cartilage element, a less-well differentiated nail and fused intermediate bones. Interestingly, Ihh is expressed at the tip of Shh mutant limbs and could account for formation of distal structures. In contrast to previous studies we also demonstrate that Shh signaling is required for maintenance of normal Fgf8 expression, since expression of Fgf8, unlike some other AER marker genes, is rapidly lost from anterior to posterior after E10.5, with only a small domain of Fgf8 expression remaining posteriorly. Furthermore, loss of expanded Fgf8 expression is paralleled by a collapse of the handplate. Our data show that development of most intermediate elements of the hindlimb skeleton are Shh-dependent, and that Shh signaling is required for anterior-posterior expansion of the AER in both limbs and for the subsequent branching of zeugopod and autopod elements. Finally, we show that Shh is also required for outgrowth of the limb ectoderm and thus for the formation of a distinct limb compartment. (C) 2001 Elsevier Science Ireland Ltd.
AB - Patterning of the limb is coordinated by the complex interplay of three signaling regions: the apical ectodermal ridge (AER), the zone of polarizing activity (ZPA), and the non-ridge limb ectoderm. Complex feedback loops exist between Shh in the ZPA, Bmps and their antagonists in the adjacent mesenchyme, Wnt7a in the dorsal ectoderm and Fgfs in the AER. In contrast to the previously reported complete absence of digits in Shh(-/-) mice, we show that one morphologically distinct digit, with a well-delineated nail and phalanges, forms in Shh(-/-) hindlimbs, while intermediate structures are severely truncated and fused. The presence of distal autopod elements is consistent with weak expression of Hoxd13 in Shh(-/-) hindlimbs. Shh(-/-) forelimbs in contrast have one distal cartilage element, a less-well differentiated nail and fused intermediate bones. Interestingly, Ihh is expressed at the tip of Shh mutant limbs and could account for formation of distal structures. In contrast to previous studies we also demonstrate that Shh signaling is required for maintenance of normal Fgf8 expression, since expression of Fgf8, unlike some other AER marker genes, is rapidly lost from anterior to posterior after E10.5, with only a small domain of Fgf8 expression remaining posteriorly. Furthermore, loss of expanded Fgf8 expression is paralleled by a collapse of the handplate. Our data show that development of most intermediate elements of the hindlimb skeleton are Shh-dependent, and that Shh signaling is required for anterior-posterior expansion of the AER in both limbs and for the subsequent branching of zeugopod and autopod elements. Finally, we show that Shh is also required for outgrowth of the limb ectoderm and thus for the formation of a distinct limb compartment. (C) 2001 Elsevier Science Ireland Ltd.
KW - Limb development
KW - Mouse
KW - Shh
KW - Sonic hedgehog
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U2 - 10.1016/S0925-4773(00)00492-5
DO - 10.1016/S0925-4773(00)00492-5
M3 - Article
C2 - 11118883
AN - SCOPUS:0035213877
SN - 2667-291X
VL - 100
SP - 45
EP - 58
JO - Cells and Development
JF - Cells and Development
IS - 1
ER -